BAJA MCQs
BAJA MCQs
BAJA MCQs
A. Salerno
B. Athens
C. Bologna
D. Alexandria
E. Montpellier
5. Herophilus was the:
A. First to dissect the human body and give the duodenum its name
around the 4th century B.C.
B. Founder of the science of Physiology
C. First to count the pulse and analyse its rate and rhythm
D. First to describe the blood pressure
E. First to count the respiratory rate and show its significance
1
6. The four cardinal signs of inflammation were first described by:
A. Galen
B. Hippocrates
C. Hunter
D. Erasistratus
E. Celsius
7. In ancient India (first century):
A. He was born in Pergamon in Asia Minor and lived from 199 to 129 B.C
B. He studied in Alexandria
C. Most of his views on physiology were correct
D. His concepts formed the theoretical basis of medicine and surgery for fifteen
centuries
E. Formulated the basis of the germ theory
9. In the early Christian era:
2
11. “No man can be a good physician who knows no surgery and conversely
on one can be a good surgeon without knowledge of medicine”. This was
said by:
A. Hugh of Lucca
B. Lanfranc of Milan
C. Theodoric of Cervia
D. Pope Innocent VI
E. Henri de Mondeville
12. Andreas Vesalius:
A. 1725
B. 1801
C. 1845
D. 1885
E. 1902
15. The Oldest Surgical College is probably:
3
16. Surgery was made a science and not just an art by:
A. William Cheselden
B. John Abernethy
C. Theodor Billroth
D. John Hunter
E. Lord Lister
17. John Hunter:
4
21. The first to demonstrate the analgesic effect of nitrous oxide was:
A. Horace Wells
B. Sir Humphrey Davy
C. Colton
D. Bigelow
E. C.T. Jackson
22. Anaesthesia was first successfully demonstrated in public:
A. Halstead
B. William Macewen
C. August Bier
D. Karl Kohler
E. John Liston
25. The germ theory of disease was established experimentally by:
A. Louis Pasteur
B. Joseph Lister
C. Jacob Henle
D. Koch
E. Summerlweiss
5
26. Joseph Litser:
A. Introduced asepsis
B. Used carbolic acid to dress wounds, sterilize instruments and spray
the air in the operating area
C. Was Professor of Surgery in University College Hospital, London
D. Influenced Volkmann, Lagenbeck and Thiersh
E. Is accredited with the germ theory of disease
27. Steam sterilization of surgical dressings, gowns and towels was
introduced by:
A. Volkmann
B. Ernst von Bergmann
C. Neuber
D. Lister
E. Lagenbeck
28. Theodor Billroth:
6
31. The first successful salpingectomy for ruptured ectopic pregnancy
was done by:
A. Spencer Wells
B. Lawson Tait
C. Anton Wolfler
D. Thomas Morse
E. Summelweiss
32. Early gynaecological surgeons included:
A. Spencer Wells
B. Marion Sims
C. Sir Frederic Treves
D. Lawson Tait
E. Sir John Eric Erichson
33. Sir William Macewan:
A. Worked in London
B. Was the father of neurosurgery
C. Was the first to diagnose a cerebral abscess and successfully operate for
extradural haemorrhage
D. Introduced the endotracheal tube
E. Introduced use of bone wax to control haemorrhage in neurosurgery
34. Early neurosurgeons included:
A. Victor Horsley
B. E.C. Cuther
C. Harvey Cushing
D. Halstead
E. Robert Gross
35. Cardiac surgery was first pioneered in:
A. New York
B. Boston
C. Edinburgh
D. Vienna
E. Paris
36. Early cardiac surgeons included:
A. Robert Gross
B. Clarence Craaford
C. Henry Souttar
7
D. John Strieder
E. Alfred Blalock
8
42. Discoverers of the blood groups included:
A. Splenectomy
B. Done by Muhe
C. In 1985
D. Done in France
E. Done without anaesthesia
44. Laparoscopic surgery compared to open surgery generally:
A. Reflux oesophagitis
B. Adrenalectomy
C. Oesophagectomy
D. Partial gastrectomy
E. Pancreatectomy
46. In the future, it may be possible to do appendicectomy via:
A. The mouth
B. Vagina
C. The anus
D. A port opening in the anterior abdominal wall
E. Perineum
47. In telesurgery:
9
CHAPTER 1
SHORT HISTORY OF SURGERY
ANSWER
1. C 34. A, C
2. A, B, C 35. B
3. A, B, C, D, E 36. A, B, C, D, E
4. A 37. B
5. A, C 38. A, C, D
6. E 39. A, C
7. B, C, D 40. A, B, C, D, E
8. B, D 41. C
9. B, C, D, E 42. B, D, E
10. A, B, C 43. B, C
11. B 44. A, B, C
12. B, C, D, E 45. A, B, C, D
13. C, D 46. A, B, C
14. C 47. A, B, D
15. A
16. D
17. A, C, D, E
18. A, B, C, D, E
19. A, B
20. D
21. B
22. A, C, D
23. A, C
24. B
25. A
26. B, D
27. B
28. A, B, C, E
29. B, C
30. A, C, E
31. B
32. A, B, D
10
33. B, C, D
CHAPTER 1
A SHORT HISTORY OF SURGERY
The oldest “book” in the world is:
Plato’s Republic
Mishnah
Sushrata Sumhita
Could do tonsillectomy
11
The first medical school was established in:
Salerno
Athens
Bologna
Alexandria
Montpellier
First to dissect the human body and give the duodenum its name
First to count the pulse and analyse its rate and rhythm
Galen
Hippocrates
Hunter
Erasistratus
Celsius
12
In ancient India (first century):
Alya (surgery) was considered the most important branch of the art of healing
Concerning Galen:
He was born in Pergamon in Asia Minor and lived from 199 to 129 B.C
He studied in Alexandria
His concepts formed the theoretical basis of medicine and surgery for fifteen
centuries
gynaecology
“No man can be a good physician who knows no surgery and conversely
on one can be a good surgeon without knowledge of medicine”. This was
said by:
Hugh of Lucca
Lanfranc of Milan
Theodoric of Cervia
Pope Innocent VI
Henri de Mondeville
Andreas Vesalius:
14
Contributed to the progress of surgery
1725
1801
1845
1885
1902
William Cheselden
John Abernethy
Theodor Billroth
John Hunter
15
Lord Lister
John Hunter:
diseases
Mandrogora
Opium
Hypnotism
John Hunter:
Did appendicectomy
Calcutta
16
MGH, Boston
France
U.C.H., London
Horace Wells
Colton
Bigelow
C.T. Jackson
17
Opposed by the church
Halstead
William Macewen
August Bier
Karl Kohler
John Liston
Louis Pasteur
Joseph Lister
Jacob Henle
Koch
Summerlweiss
Joseph Litser:
Introduced asepsis
18
the air in the operating area
introduced by:
Volkmann
Neuber
Lister
Lagenbeck
Theodor Billroth:
Appendicectomy:
19
D. Was the greatest German Surgeon of all time
E. Lived from 1841 top 1917
Spencer Wells
Lawson Tait
Anton Wolfler
Thomas Morse
Summelweiss
32. Early gynaecological surgeons included:
Spencer Wells
Marion Sims
Sir Frederic Treves
Lawson Tait
Sir John Eric Erichson
33. Sir William Macewan:
Worked in London
Was the father of neurosurgery
Was the first to diagnose a cerebral abscess and successfully operate for
extradural haemorrhage
Introduced the endotracheal tube
Introduced use of bone wax to control haemorrhage in neurosurgery
34. Early neurosurgeons included:
Victor Horsley
E.C. Cuther
Harvey Cushing
Halstead
Robert Gross
35. Cardiac surgery was first pioneered in:
New York
Boston
Edinburgh
20
Vienna
Paris
36. Early cardiac surgeons included:
Robert Gross
Clarence Craaford
Henry Souttar
John Strieder
Alfred Blalock
21
John’s Hopkins, Baltimore
Cook County Hospital, Chicago
St. Mary’s London
State Hospital, Moscow
Splenectomy
Done by Muhe
In 1985
Done in France
Done without anaesthesia
44. Laparoscopic surgery compared to open surgery generally:
Reflux oesophagitis
Adrenalectomy
Oesophagectomy
Partial gastrectomy
Pancreatectomy
46. In the future, it may be possible to do appendicectomy via:
The mouth
Vagina
The anus
A port opening in the anterior abdominal wall
22
Perineum
47. In telesurgery:
CHAPTER 1
SHORT HISTORY OF SURGERY
ANSWER
C 34. A, C
A, B, C 35. B
A, B, C, D, E 36. A, B, C, D, E
A 37. B
A, C 38. A, C, D
E 39. A, C
B, C, D 40. A, B, C, D, E
B, D 41. C
B, C, D, E 42. B, D, E
A, B, C 43. B, C
B 44. A, B, C
B, C, D, E 45. A, B, C, D
C, D 46. A, B, C
C 47. A, B, D
A
D
A, C, D, E
23
A, B, C, D, E
A, B
D
B
A, C, D
A, C
B
A
B, D
B
A, B, C, E
B, C
A, C, E
B
A, B, D
B, C, D
24
CHAPTER 2
MICROBIAL INFECTIONS
Haemostasis
Sepsis
Acute Pain Relief
Access to internal organs
Development of suture materials
Match the surgical historical events with the credited pioneer:
1
A. The Dose of the organism
B. Tissue environmental pH
C. Oxygen tension of tissues
D. Microbial synergism
establish
an infection is:
pyogenic
2
Malnutrition
Diseases of the immune system
Associated jaundice
9. Surgical infections:
3
10. Staphylococcus pyogenes:
A. Leucocidin
B. Haemolysin
C. Erythrogenic toxin
D. Hyaluronidase
E. Deoxyribonuclease
13. β-haemolytic streptococcus pyogenes:
4
E. 90% of them beleng to the Lancefield Group A
14. Streptococcus viridans:
A. Is a β-haemolytic streptococcus
B. Is a normal comensal of the Duodenum
C. Characteristically causes intra-oral infections – tonsilitis
D. May seed on to cardiac valves producing subacute bacterial
endocarditis
E. Frequently contaminates chronic leg ulcers and burns
A. Gram-ve rods
B. Responsible for pneumonic lesions
5
C. Occur in hepatic abscesses
D. Noted to contribute to wound infections after transplantation
procedures
E. A frequent cause for endotoxic shock
18. Pneumococci are:
19. A man of 60 with a week’s history of swelling of the left leg, with
fever,
malaise and anorexia and pitting oedema of the ankle is most
likely to be
suffering from:
A. Deep Venus Thrombosis of (Lt.) leg.
B. Congestive cardiac failure
C. Cellulitis of (Lt.) leg
D. Lymphaedema of the leg
E. Pyomyositis of the Lt. leg
20. The following are likely complications of Q19:
6
D. Lymphoedema
E. Pulmonary embolism
21. Treatment strategy of patient in Q.19:
A. Bed Rest
B. Elevation of affected limb
C. Immobilization of the affected limb
D. Crystaline penicillin 2 million, units 8 hourly 1/M
E. Debridement of dead and dying skin and soft tissues.
22. Cellulitis of the Scalp:
7
lower
molar teeth
C. Hemmed in by attachment of deep fascia to the hyoid bone
D. Associated with spread of inflammatory fluid along the sheath of the
stylohyoid muscle.
E. An emergency because it may precipitate asphyxiation.
25. In Ludwig’s Angina:
8
F. The Immediate antecedent may be tonsellectomy or peritonsillar
abscess.
G. Trismus and a tender mass over the parotid are the hall mark
features.
27. A Phlegmon:
A. Is a unilocular abscess
B. Is an inflammation which is spreading and diffuse
C. Usually incorporates small multiple tiny pockets of pus
D. Is usually the result of infection with mixed organisms – streps and
staphs.
E. Is often occasioned by extensive suppuration and tissue necrosis
28. An Abscess is:
9
A. The result of infection of several hair follicles
B. Produced by Streptococcus pyogenes infection
C. Seen in tissues well endowed with thick columns of fat
D. Characterised by radial spread of infection
between the skin and deep facia
E. Associated with ischaemic necrosis
30. Carbuncles:
10
33. The Systemic Inflammatory Response Syndrome (SIRS):
Infection) include:
11
37. Currently the organism responsible for most wound infections on
surgical
wards is:
Streptococci
Staphylococci
Pneumococci
Haemophilus influenza
Proteus organism
38. This organism is to be found in:
A. Pharynx of 5-10 per cent of the population
B. The anterior nares of about 50 per cent of the population
C. The upper respiratory tract of normal people
D. The oral cavity of normal people
E. Lower gastro-intestinal tract of patients
39. Which of the following clinical conditions may be regarded as
common
sequelae of cellulitis of the limb seen in the tropical environment?
risk?
12
A. Neck
B. Scalp
C. Orbit
D. Philtrum of upper lip
E. Anterior nares
follicles?
A. Cellulitis
B. Carbuncle
C. Vesicle
D. Pyoderma gangrenosum
E. A macule
42. The danger from bacteraemia lies particularly in:
13
Rapid diminution of urinary output in face of adequate hydration
Normal red cell count.
44. Match the following forms of synergistic Gangrene/Cellutitis with
their
causative organisms:
Melaney’s Gangrene
Ulcerative Gingivitis
Cancrum Oris
Necrotising Fasciitis
Fournier’s Gangrene
14
occur
include the following:
Road Traffic Accidents
Injuries in agricultural fields
Deep wounds with muscle damage
Foreign body containing wounds
Some physiological wounds – birth wounds
47. In tetanus wound Infection:
15
E. In the active form traditionally requires a dose of toxoid at intervals
of
weeks and 6 months.
F. Can be rapidly induced with 3 doses on day 1, 4 and 7
50. In Tetanus prophylaxis:
of:
16
C. Specialised Intensive Care Unit
D. General Ward Services
E. Dependable Ambulatory Service Unit
F. A Directing Team: Physician, Surgeon, Anaesthetist
53. Mild Cases of Clinical Tetanus:
pressure mechanism
17
56. In the Dangerously ill patient with clinical Tetanus Significant
prognostic
signs include:
Pronounced tachycardia
Severe Diaphoresis (Sweating)
Wide fluctuations of the blood pressure
Intense peripheral vaso constriction
Increased Urinary excretion of catecholamines
(> 1000ugm/day)
57. In patients dangerously ill with Tetanus:
A. The causative organisms Cl. welchii, Cl. perfringens, Cl. novy, Cl.
oedematiens
Cl. septicum are sacharolytic
B. The causative organisms Cl. sporogenes, and Cl. haemolyticus are
proteolytic
C. The most important toxin produced is the α-toxin
D. The anaerobic organisms are introduced more often by faecally
contaminated cloathing
E. Excessive haemorrhage and use of tourniquet are predisposing
causes.
59. In Gas Gangrene:
18
C. Retained foreign bodies do not affect the outcome of management
D. The causative organism may be autogenous (gastric and biliary
mucosa)
E. The lower limbs are more often affected than the upper limbs.
19
there is rapid
painful swelling of the stump within 24 hours, with oedema, and
discharge
of blood stained brownish exudates from a drain placed in the
wound. The
patient feels unwell but she is apyrexial, not anaemic and has a
pulse of
100min.
(s):
20
management
C. Irrigation of the wound and packing with gauze wrung in H202 is of
no
value
D. Crystalline Penicillin 10 mega units a day – with metronidazole and
clindamycin together is better than penicillin alone
E. Polyvalent antitoxin 15,000 unit/Kg body wt. is essential
F. Hyperbaric oxygen is of little practical value
65. The distinction between Clostridial myonecrosis and necrosting
fasciitis
21
A. The antibiotic of choice is ciprofloxacin
B. The antibiotics must be given for a minimum period of 5days
C. The beneficial effects of antibiotics are evident within 72 hours
D. Care must be taken to ensure adequate nutrition
E. Monitoring to ensure against subsequent functional damage to
lymphatics
68. Anthrax:
22
70. The Intestinal form of Anthrax is:
23
A. A 10-14 days period of observation of the suspects is mandatory
B. The incubation period is shorter for facial and trunk bites
compared
with bites on the limbs
C. Pain at the site of the bite is the most important early symptom
D. The hydrophobia is produced by laryngeal muscle spasm
E. The Diagnosis is confirmed by the finding of Negri bodies in the
brain
74. In the management of Rabies:
A. Prophylactic human diploid vaccine (HDCV) is the most effective
measure
B. The vaccine should be given immediately after exposure
C. Pre-exposure prophylaxis is essential for animal handlers
D. Where risk from rabies is serious combined rabies antiserum and
vaccination gives best protection
E. Thorough irrigation of the wound with soap reduces the number
developing
clinical rabies
F. Thorough wound irrigation lowers the mortality from 90% to 5%
G. It is safer to leave the wound unsutured
H. Tetanus toxoid and antibiotic should also be given
24
disease,
a 70-year old man develops fever, tachycardia, weakness with
intense
wound pain and rapid swelling and oedema of the stump. The
patient
rapidly becomes anaemic and 24 hours later becomes mildly
icteric; there
is evidence of impaired peripheral circulation and his 24-hour
urinary output
is about 600ml.
transmit rabies?
A. Bat
B. Squirrel
C. Horse
D. Cattle
E. Cat
25
78. Currently which of the following do you consider the most
effective first line
regime against the mycobacterium tuberculosis?
yaws?
A. Pyoderma gangrenosum
B. Pachyderma keratitis
C. Scaling dermatitis of the palm
D. Erythema nodosum
E. Lymphoedema of the affected foot
80. A young man of 25 presents with a painless, firm round ulcer on
the glans of
the penis which develops two weeks after sexual exposure. He
has no
systemic symptoms.
26
He is most likely to be suffering from:
Chancroid
Syphilis
Genital herpes
Aphthous ulcer
Lymphogranuloma venereum
A. Fingers
B. Anal canal
C. Lips
D. Inner thigh
E. Tongue
82. Which of the following chemotherapeutic agents exert their
influence by
dissolution of the cell wall of the organisms?
Penicillin
Cephalosporins
Lincomycin derivatives
Cloxacillin derivatives
Nystatin
83. Which of the following chemotherapeutic agents act by
competition with the
organisms for substrate by influencing the ribosomes inhibiting
protein
27
synthesis?
Sulphadimidine
Tetracycline
Chloramphenicol
Erythromycine
Gentamicin
84. Prophylactic antibiotic therapy is justified in:
28
Age of the patient
Haematoma formation
87. Which of the following factors is/are considered as significantly
affecting the
development of post-operative wound infection?
Glove punctures
Nasal carriage-patient and staff
Emergency operation
Skin towels
Skin carriage of organisms
88. Which of the following may be considered as effective means of
preventing
hospital infection?
Removal of the sources and reservoir of infection
at:
A. 10-15˚C
B. 15-20˚C
C. 20-25˚C
D. 25-30˚C
E. 30-35˚C
29
90. The humidity in the operating theatre should ideally be:
30
countries
C. Is responsible for boils, carbuncles, breast abscesses and
osteomyelitis
D. Produces the exotoxin--toxin
E. Is usually sensitive to cloxacillin, lincomy cin and cephalothin
94. Streptococcus pyogenes:
31
97. Cellulitis of the limb:
32
culture
results are known
their main
braches
E. Should be treated with appropriate antibiotics and early
surgical
decompression of the space
101. Cellulitis of the pharyngo-maxillary space:
33
feature
of treatment
E. Shows a strong tendency to recurrence
102. A carbuncle:
103. Bacteraemia:
34
A. Implies invasion of the circulation by actively multiplying
organisms
B. Arises from intravascular septic foci, e.g. abscesses,
infected
thrombosis
C. Is announced by chills and rigors and profound prostration
D. Usually produces significant leucocytosis with a shift to the
left
and a disappearance of eosinophils
E. Is associated with a severe hypercatabolic state with
marked
weight loss
105. Tetanus:
35
106. Modern management of tetanus:
36
109. The severely ill patient with clinical tetanus:
37
C. Usually has his spasms best controlled by succinyl
choline
D. Has a mortality of at least 10-15 per cent
E. Does better if a sympatholytic agent such as bethanidine
is added
to the treatment regime
38
C. Readily establishes in deep wounds contaminated by
clostridia
and aerobic organisms
D. Develops 48 hours after injury
E. Invariably gives rise to tissue clostridial
114. Gas gangrene:
115. Erysipelas:
39
subcutaneous
tissues
E. Responds briskly to crystalline penicillin in doses of 1 to 2
mega l/M
units daily
117. Erysipelas:
119. Anthrax:
40
B. Shows a predilection for the lymphoreticular system
C. Is most contagious in its intestinal form
D. May lead to pulmonary oedema which is rapidly fatal
E. May be treated with tetracycline in penicillin sensitive
individuals
although less effectively
120. Clinical Rabies:
41
122. Clinical Rabies:
42
124. Primary tuberculosis:
43
the organism
C. Is usually associated with active pulmonary lesions
D. In the later stages the glands are matted together through
periadenitis
E. Should be treated in later stages (sinuses) by excisional surgery
of gland and sinuses and skin grafting
127. Regarding Tuberculosis:
44
Through the joints and long bones in early septiaemia
129. Primary Pulmonary Tuberculosis:
A. Resolution
B. Calcification
C. Fibrosis with matting together
D. Haemorrhagic infarction
E. Caseation and formation of a Collar-stud abscess
45
132. A Ghanaian male of 30 presents with a painless cervical
swelling below
the level of the angle of the mandible of six weeks duration. He
admits
to a period of anorexia, malaise and weight loss but denies
coughs and
night sweats. The swelling is firm, discrete, and non tender.
There are
no other cervical swellings:
A. Bronchial cyst
B. Degeneration of lymphatic metastases
C. Suppurative lymphadenitis
46
D. Collar stud Abscess (Cold Abscess)
E. Cervical Dermoid
F. Lipoma
G. Cystic hygroma
134. A man of 70 presents with a chronically discharging cervical
sinus at the
level of the angle of the mandible, of two months duration. He
admits to
recent coughs with rusty spectrum but denies pyrexia and night
sweats.
47
by:
Site of TB lesion: pulmonary or extra pulmonary
Result of sputum smear: positive or negative
Previous anti TB treatment
Severity of TB infection
Appearance of Resistant Strains
48
and Rifampicin
C. The most effective Drugs are Isoniazid and Rifampicin
D. Isoniazid, Rifampicin Pyrazinamide and Ethambutol are
recognized as hepatoxic
E. Streptomycin is potentially Ototoxic and causes deafness in
babies - best
avoided.
Cross-reaction of HIV therapy with Rifampicin may be life
threatening
49
units daily for 6 weeks
142. Actinomycosis:
A. Is a granuloma
B. Is firm and nodular
C. Has indefinite edges
D. Usually spreads along fascial planes
E. Seldom spreads along lymphatics to lymph nodes
144. Actinomycotic infections:
50
E. Show a predilection for the face, chest and the liver
145. Cervico-facial actinomycosis:
A. The organism reaches the liver via the portal vein, hepatic artery
or from contiguous pulmonary lesions through the diaphrgram
B. There is rapid liver necrosis
C. The liver is riddled with numerous abscesses
D. There is progressive cachexia
E. The diagnosis is usually made at laparotomy
F. Jaundice is invariable at presentation.
51
148. In Ileocaecal actinomycosis:
150. Yaws:
52
pleomorphic rashes
E. Responds equally to neosalvan, bisttmuth and P.A.M.
151. Yaws:
53
C. Is responsible for destructive lesion of the hand and soft palate
and the nasal cartilages and bones
D. Is responsible for that deformity of the face called Goundou
E. Usually spares the long bones of the body
154. In Yaws (Framboesea):
54
lesion
C. The rashes differ from syphilis in being asymmetrical in distribution
D. By auto innoculation older lesions are surrounded by new
generation
of daughter papules
E. The typical yaw when fully developed is an escresence with
yellowish
crust raised 0.5-2cm above the skin
F. Healing of the lesions leaves pigmented spots especially on the
palms and hands
157. The Lesions of Tertiary Yaws include:
55
159. Gonorrhoea:
56
162. Non-gonococcal urethritis:
57
D. Is associated with painful nocturnal erections
E. Is confirmed by the finding of haziness in both glasses in the
two glass test
F. May show as an exquisitely tender and fluctuant prostate
58
one month
168. Gonococcal infection in the female:
59
In its primary or secondary form is best treated with procaine
penicillin in doses of 600,000 units daily for 15 days
171. Syphilis:
60
C. May present as isolated cranial nerve palsies
D. Is best treated by a course of penicillin aluminium monostereate
1.2 mega units twice weekly for seven weeks
E. Is not attended by reversion of serological tests to normal
after treatment
173. Tertiary syphilis:
A. The more recent the infection in the mother the greater the
probability and severity of the disease in the infant
B. Diagnosis of the early lesion needs to be confirmed by isolation
of
Treponema pallidum from the mucosal and skin lesions
C. Radiological changes in the skull and long bones are usually
present
D. The neurological and cardiovascular changes occur about the
time
of puberty
E. Treatment should primarily be through prophylactic treatment of
the
61
mother
175. In congenital syphilis:
62
D. The Primary lesion does not show contact bleeding
E. There is marked regional lymphadenopathy
F. There is little or no systemic reaction to the infection
178. In Primary Syphilis:
63
D. Itching is intense
E. Serological tests are usually positive and prove useful in differential
diagnosis
F. The mucosal lesions invade deeply the cheek and bucal mucosa
with risks of secondary haemorrhage.
G. Raised flat topped condyloma appear at mucocutaneous junctions
–
anal, vula, mouth
H. Generalised lymphadenopathy is common
I. Lymphadenopathy is symmetrical
180. In the Management of Primary and Secondary syphilis:
A. The basic lesions are evident within a year of onset of the disease
B. The basic lesion is an extensive necrosis bordered by epitheliod
64
cells
C. The basic lesion is the gumma, a necrotic granuloma
D. The necrotising lesions leave ulcers that are typically under mined
E. The necrotizing lesions produce punched out ulcers
F. The resulting ulcers heal leaving tissue paper thin scars
G. The cutaneous lesions show a predilection for the bony areas of
the leg and forearm
H. The tongue may show superficial atrophic glossitis
I. The tongue may show interstitial glossitis with leukaplakia
J. Perforation of the palate and nasal septum may occur
182. In Tertiary Syphilis:
65
A. Abortion in the first trimester
B. Still birth at term
C. Premature labour with maceration of the foetus
D. Normal child developing signs within first few weeks at home
E. Normal child developing signs in later childhood
F. Child without clinical signs or serological changes
184. Early Congenital Syphilis:
66
A. Is caused by the common herpes virus
B. Is encountered in both sexes
C. Is characterized by itching in the glans as the first symptom
D. Usually presents as an area of vesicular rashes and excoriations
of
the glans and prepuce
E. Is treated with sulphadimidine 1G qds for 5 days and topical
1 per cent hydrocortisone cream
187. Genital Herpes:
67
189. Lymphogranuloma venereum:
68
192. In Lymphogranuloma Venereum in the Female:
69
194. In the treatment of lymphogranuloma venereum the preferred
option is:
70
197. In HIV AIDS infection:
71
Persistent Generalised lymphadenopathy
sarcoma
72
There are symmetrical facial plaques
There is often leg oedema and pulmonary infiltrates
The lesion is mainly visceral in HIV in patient
The Human Herpes Virus 8 (HHV8) is encountered only in the HIV
associated kaposi sarcoma.
A. Routine testing of all patients cuts down the risks to the surgeon
B. It is pragmatic to assume that the risk in all procedures is significant
C. Wearing masks and goggles when using endoscopes and bone
and
dental drills has no protective value
D. Skin Contact with body fluids carries little risk
E. Wound irrigation entails no risk to the health attendant
203. The major risk factors of occupationally acquired HIV infection
include
the following except:
Puncture Wound
Visible blood on the injuring device
Placement of hollow needle in a vessel
Working on patients with late stage HIV
Contact with the intact skin.
204. The Recommendation for post-exposure prophylaxis (PEP) for
health care
workers include:
73
Action should be instituted within 2- 4h of injury
Washing skin with soap and water
The contaminating source is tested for HIV
In HIV +ve Class 1 source exposure the 2 drug post exposure
prophylaxis
is advised (zidovudine + lamivudine)
In HIV +ve Class 2 source exposure the 3 drug post exposure
prophylaxis
is advised (zidovudine, lamivudine and indinavir)
In mucous membrane exposure large volume exposure requires a
two
drug post exposure prophylaxis
HIV Tests of the worker should be done at 6 weeks, 3, 6 months
and
1 year
74
than they are in preventing them
D. Which are bactericidal generally act by dissolution of the cell
walls
of the organisms
E. Should always be given with vitamin supplements in all patients
207. In the general use of antibiotics in surgery:
75
Appendicectomy for acute appendicitis
Appendicectomy for perforated appendicitis
Appendicectomy for gangrenous appendicitis
Splenectomy for trauma in a 40 year old man
Repair of tendons severed by a Kitchen knife
209. In the prophylactic exhibition of antibiotics:
76
D. Has a preference for the unit air conditioner
E. Makes provision for sterilization facility within the suite
212. Which of these organisms is noted to be a particularly
dangerous cause
for epidemic nosocomial infection:
Site
77
infection (SSI) is:
Location in a cul-de-sae
Separation of sterilization from theatre suite
Elimination of shelves
Tiled theatre walls
Plenum ventilation with air changes of 20 per hour
Temperature range of 18-25°C
Humidity of 55-65%
Physical barriers protecting the clean areas of the theatre
78
217. Antibiotics:
A. Should be recognized as adjuncts and not substitutes for
indicated
surgical therapy
B. May considerably mask the signs of infective processes
C. Are more effective in the early cellulitic and hyperaemic stages
of infection
D. May be given prophylactically at the time of drainage of
abscesses
E. Used therapeutically must be assessed continuously with respect
to development of side effects
CHAPTER 2
79
MICROBIAL INFECTIONS
ANSWERS
1. A, B, C 38. B 75. D
2. A1, B2, C3, D4, E5 39. B 76. A, B, C, D
3. B 40. A, B, C, D, E 77. A, B, C, D,
E
4. A, B, C, D, E 41. B 78. B
5. A 42. A, B, C 79. C
6 C 43. A, B, C, D 80. B
80
24. A, B, C, D, E 61. E 98. A, C, D
25. A, B, C, D, E, F, G, H, I 62. D 99. A, B, C, D,
E
26. A, B, C, D, E, F, G 63. A, B, C, D 100. A, C, D, E
81
128. A 166. A, B, C, D, E, F, G 204. A, B, C, D, E,
F, G
129. A, C 167. B 205. B
130. C, D 168. A, B, C, D, E, F 206. A, B, C, D
131. A, B, C, E 169 A, B, C, D, E 207. A, B, C, D, E
132. D 170. A, B, C, D, E 208. C, F
133. D 171. C, E 209. A
134. D 172. A, B, C, D, E 210. A, B, C, D, E
135. B 173. A, B, C, E 211. B, C
136. A, B, C, D, E 174. A, B, C, D, E 212. D
137. A, B, C, D, E 175. A, B, C, D 213. A, B, C, D, E
138. D 176. A, D, E 214. E
139. A, B, C, D, E, F 177. A, C, D, E, F 215. E
140. A, B, C, D 178. A, B, C, D, E, F 216. A, B, C, D, E,
F, G, H
141. A, B, C, D, E 179. A, B, C, E, H, I 217. A, B, C, D, E
142. B, D, E 180. B, C, D, E, F
143. A, B, C, D, E 181. C, E, F, G, H, I, J
144. A, B, C, D, E 182. A, C, E
145. A 183. A, B, C, D, E, F
146. A, B, C, E, G 184. C
147. A, C, D, E 185. D
148. A, B, C, D, E, F 186. A, B, C, D, E
149. A, B, C, D, E 187. B, D
82
83
84
CHAPTER 4
A 40 year old man reports at your consulting room with a history of “Prolonged
period of ill health” for which he has consulted several prayer camps and
traditional healers without improvement. No other relevant information is available.
The highlights of your examination shows the following:
47. Which of the following drugs would you use to treat a diagnosed case of
s.mansoni in a 40 year old lady?
A. Praziquantel
B. Metrifonate
C. Stibophen
D. Oxamniquine
E. Niridazole
48. Certain nematodes pass through the lungs during their developmental stages in
man. They include:
A. Dracunculus medinensis
B. S.mansoni
C. Wuchereria bancrofti
D. Onchocerca volvulus
E. S.japonicum
49. Mass suppressive treatment with appropriate drugs is one of the methods used
to control schistosomiasis. Strategies under this method are:
A. Multiphasic chemotherapy
B. Selective population chemotherapy
C. Mass chemotherapy
D. Targeted chemotherapy
E. Oppurtunistic chemotherapy
50. Other methods of control of schistosomiasis are environmental measures such
as:
A. Provision of toilet facilities in the vicinity of recreational swimming places
B. Construction of foot bridges at water crossing points
C. Construction of irrigation schemes that encourage stagnation of the irrigation water
D. Wearing of rubber boots or other protective clothing for people who by necessity
need to wade through water bodies
E. Vigorously toweling the skin surfaces 24 – 48 hours after contact with suspected
water with application of 40% alcohol to the skin
CHAPTER 4
INFECTIONS BY NEMATODES AND TREMATODES
ANSWERS
1. B, D, E 38. A
2. A, B, C 39. B, C, D
3. D 40. A, B, C
4. A, B, C, D 41. A, B, D
5. C 42. A, B, C, D, E
6. A, C, D, E 43. B
7. B 44. B, D, E
8. E 45. A, B, D
9. A 46. A, B, D
10. A 47. A, D, E
11. B 48. B, E
12. A, B, C, D 49. B, C, D
13. A, B, C, E 50. A, B, D
14. B, C
15. D
16. C
17. B, D
18. B, E
19. A, C, D, E
20. A, B, E
21. -
22. E
23. A, B, C
24. B, C
25. B, D, E
26. A, B, C, E
27. A, C
28. A, B, C, E
29. A, B, D
30. B, D, E
31. A, B, C
32. A, B, C, D
33. B, C, D, E
34. A, B, C, D, E
35. B, C, D
36. A, C
37. C, E
CHAPTER 6
CUTANEOUS ULCERS, SINUSES, FISTULAE
1
Chronic osteomyelitis of the underlying bone
Tetanus
Lymphoedema of the foot
Malignant change in the ulcer
Rifampicin
Clofazimine
Streptomycin
Co-trimoxazole
INAH
An ulcer of yaws:
May start as a granulomatous papule
Has sloping edges
Has dirty yellowish sloughing floor
May heal spontaneously, the skin over it becoming depigmented
2
Does not cause enlargement of regional lymph nodes
An ulcer:
A non-specific ulcer:
In the acute phase is painful and has a sloughing floor covered with
purulent discharge and a sharp edge with oedematous tender
surrounding skin
In the transition phase has a sloping edge and grayish-yellow floor.
In the reparative or healing phase is painless and pink granulation
fills the floor
In the chronic phase has grayish floor with a thin odourless
discharge
The fifth phase is malignant change
In an indolent or callous ulcer, the:
Base is indurated
Floor has pink granulation tissue
Edges are rigid and hard
Surrounding skin is warm and oedematous
Epthelium at the edge grows inwards
Complications of non-specific ulcers of the lower leg include:
Chronic osteomyelitis
Amyloidosis
Below knee lymphoedema
Deformities of the foot or ankle
Venous thrombosis
A painful circular ulcer with sloping edges on the dorsum of the
foot near the big toe in a 60-year old man could be due to:
Leprosy
Varicose veins
3
Arterial disease
Malignant melanoma
An abscess
The prime cause of a venous ulcer following deep venous
thrombosis is:
Varicosity of the long saphenous vein
Venous stasis
Back pressure in the veins
Destruction of the valves of the perforating and deep veins
High venous pressure in the legs
A venous ulcer usually:
Is situated just above the medial malleolus
Is irregularly circular
Has a deep floor with pink granulation
Has punched out edges
Has indurated base
4
Haemoglobinopathic ulcer:
Is most often found in the lower limb close to the lateral malleolus
Is associated with atrophic skin and hyperpigmentation
Heals quickly
Often breaks down again after healing
Bed nest worsens it
Haemoglobinopathic ulcer is difficult to treat because of:
Lowered oxygen tension
Recurrent haemolytic crisis
Fibrosis around the ulcer
Low haemoglobin level
Lack of appropriate personnel
A 50-year old man has a 0.5cm ulcer on the nose which has a
raised and rolled up edge. It is of 2/12 duration.
A sinus:
Connects two epithelial surfaces
May be congenital
Has a discharge which is always present
Is treated with antibiotics
Unresolved infection may cause acquired sinus.
Causes of a sinus include:
Chronic ulcer
Achnonycosis
Amyloidosis
Buruli ulcer
Foreign body e.g. Sutures
In the treatment of a sinus:
Excision of sinus is indicated in congenital type
Dressing alone adequate for acquired type
5
Tract of the sinus may be laid open and dressed
In tuberculous, sinus treatment of TB lesion leads to healing
Penicillin exhibition contributes to healing
Causes of acquired fistula include:
Abscess that ruptures into a cavity and skin
Burns
Granulomatous lesions
Benign tumours
Schistosoma haematobium
The following are examples of neoplastic ulcers:
Squamous cell carcinoma
Renal cell carcinoma
Kaposi sarcoma
Malignant melanoma
Dermato fibrosarcoma Protuberans
Diabetic Ulcer:
Ulcers in a patient with Diabetes Mellitus
May be caused by infection
May be caused by trauma
May be caused by pressure necrosis
Basis in hypoaesthesia from blood loss
6
May be associated with tuberculous bone infection
In Buruli ulcer differential diagnosis of the pre ulcerative form
include:
Onchocercoma nodule
Lipoma
Sebacous cyst
Naevus
Phyconycosis
Complications of Buruli ulcer include:
Anaemia
Contracture
Proximal lymphoedena
Marjolin’s ulcer
Osteitis
In the treatment of Buruli ulcers the following practitioners are
involved:
Physiotherapist
General Surgeon
Orthopedic Surgeon
Opthalmologist
Maxilloficial Surgeon
CHAPTER 6
CUTANEOUS ULCERS, SINUSES, FISTULAE
ANSWER
A
A, C
7
C, D
A, B, C
A, B, C
B, C, D, E
B
B
A, B, D
A, C
C, D
C, D
A, C
A, C
C, D
C, E
D
A, B
B
A, B, E
A
B, D
A, B, C, D
E
B
B, E
A, C, D
A, C
A, B, C, D
A, B, C, D
D, E
A, C, E
A, C, E
A, B, D
A, C
8
CHAPTER 8
SHOCK
The capillaries
The venules
Only about one-fifth of the capillaries are normally open at any one
1
time
Histamine
Bradykinin
Kallidin
Beta-receptors
Adrenaline causes:
Constriction of veins
2
Vasodilatation of coronary arterioles
Angiotensin:
Is a powerful vasopressor
Diminished G.F.R.
Anaerobic glycolysis
In haemorrhagic shock:
Immunity is depressed
3
A. Venous return is reduced
C. Vasoconstriction is marked
ACTH
4
Glucagon
Cortisol
Histamine
Nor-adrenaline
Cold extremities
Restlessness
Oliguria
Anxiety
Hypertension
Cold skin
Pale conjunctivae
Restlessness
5
Rapid deep respiration
Aortic bodies
Cardio-inhibitory centre
Adrenal cortex
Subfornical organ
Pancreas
Dextran 70:
Causes hypervolaemia
6
Prevents adhesiveness of platelets
Extravascular dehydration
Anaphylactic shock
Isoproterenol
Nor-adrenaline
Dopamine
Phenoxybenzamine
Chlorpromazine
Isopreterenol
Dopamine
Phenoxybenzamine
7
Chlorpromazine
Dobutamine
Dopamine:
In haemorrhagic shock:
8
Central venous pressure
Colour of conjunctivae
Metabolic alkalosis
9
In shock lung adult Respiratory Distress Syndrome (ARDS):
Oxygen toxicity
Endotoxin:
10
The following are released in septic shock:
Histamine
Thromboxane A2
Serotonin
Kinins
In septic shock:
Septic shock:
11
Is not caused by skin infections
There is hypoventilation
Sweating
Hypotension
Pallor
12
Bradycardia
Loss of consciousness
Cardiogenic shock:
In anaphylactic shock:
Adrenaline
13
Antihistamine
Hydrocortisone
Aminophylline
Intravenous fluid
Hypovolaemic shock
Septic shock
Malaria
Anaphylactic shock
Peritonitis
Intravenous antibiotics
Intravenous hydrocortisone
Intramuscular chloroquine
B-endorphin:
14
Is an opiate antagonist
Kinins
Prostacyclin
Thromboxaine A2
Serotonin
TNF – a, IL – 8
Nitric oxide
15
Coronary microvascular damage
Thrombomodulin is elevated
Protein C is raised
Protein S is raised
AT III is raised
TNF
IL -1
IL -4
IL -6
IL - 10
16
Activation of neutrophils in septic shock leads to:
Tissue infiltration
Production of anti-oxidants
Metabolic alkalosis
Depletion of anti-oxidants
DIC
Hyperkalaemia
In septic shock:
There is thrombocytopaenia
In neurogenic shock:
17
The arterioles and venules of the muscles are constricted and those
of the skin dilated
CHAPTER 8
SHOCK
ANSWERS
A, C 30. A, B, C, D, E
D 31. B, C, D
A, D, E 32. A, B
A, B, C, D, E 33. A, C, D
A, B, D 34. B, D
A, C, D 35. D
A, B, E 36. A, C, D
A, B, C 37. A, B, D, E
18
A, C 38. A, B, C, D, E
A, B 39. B
A, D 40. A, B, C
C 41. D, E
B, 42. C
A, B, C, D 43. A
A, B, D 44. B, C
A, B, C, D, E 45. B, C
A, B, C, D 46. A
A, B, C, D 47. A, D
A, B, C, D 48. A, B, E
A, C, D, E 49. A, C, D
B 50. B, D
A, B, C 51. B, C
D
D
A, B, C, D
A, B, D, E
A, B, D
B, C, D, E
A, D
19
CHAPTER 10
PRINCIPLES OF FLUID AND ELECTROLYTE THERAPY AND
ACID-BASE DISTURBANCES
1
For a cut-down, a mask and gloves should be worn
With the standard drip set, the number of drops per minute is
determined by multiplying the number of litres to be given in 24h by
10
The drip set, needle and vein should be changed every 24h
The giving set should be sterilized with ethylene oxide
Water is 3500 ml
Sodium is 130 mmol
Potassium is 70 mmol
Glucose is 50 g
Vitamin C is 100 mg
A litre of Ringer’s lactate contains in mmols:
Sodium 130
Potassium 2
Calcium 6
Chloride III
Bicarbonate 23
Three litres of the following fluids, if given throughout the 24-h
period to an adult, can provide the daily water and sodium
requirements?
Normal saline
Badoe’s maintenance solution
Ringer’s lactate
Fluid 5:4:1
5 per cent dextrose in normal saline
A litre of Darrow’s solution contains in mmols:
2
Potassium 26
Sodium 124
Chloride 104
Bicarbonate 56
Calcium 4
Potassium in adequate amounts occurs in:
Citrus fruits
Tomato juice
Coconut milk
Tea
Meat soup
Shock
Typhoid perforation
Burns
Severe metabolic alkalosis
During management of diabetes mellitus with soluble insulin
In the treatment of hyperkalaemia the following may be used:
Magnesium sulphate
Insulin
Glucose
Calcium chloride
Normal saline
Clinical features of hypokalaemia include:
Lethargy
Vomiting
Hiccough
Hyporeflexia
Paraesthesia
A litre of gastro-intestinal replacement solution contains:
3
Glucose 50 g
In the early phase of dehydration due to peritonitis, the serum
concentration of:
Sodium is normal
Potassium is increased
Chloride is increased
Urea is low
Osmolality is increased
Vomiting
Peritonitis
Diarrhoea
Burns
Enterocutaneous fistula
The ideal solution to use in rehydrating a dehydrated patient
without acid-base disturbance is:
Normal saline
5 per cent dextrose in normal saline
Ringer’s lactate
Badoe’s maintenance solution
Darrow’s solution
The reliable parameter during rehydration of a dehydrated patient
is:
4
Central venous pressure
Hourly urine output
Half-hourly pulse and blood pressure
A litre of diarrhoeal stools contains on an average about:
Ringer’s lactate
Darrow’s solution
Fluid5:4:1
Normal saline + potassium
Dextrose/saline + potassium
Clinical features of hypokalaemia include:
Convulsions
Paralytic ileus
Hypotension
Nausea
Drowsiness
5
The serum electrolytes (mmol/l) of a patient are Na: 130, K:3.2, Cl:
90, HCO3: 30. The blood urea is 9 mmol/l and the pH 7.46.
Diarrhoea
Peritonitis
Gastric outlet obstruction
Renal failure
Entero-cutaneous fistula
The best treatment will be:
The serum electrolytes (mmol/l) of an ill patient are Na: 135, K: 3.8,
Cl: 95, HCO3: 24. The blood urea is 7.5mmol/l and the pH 7.4. The
diagnosis may be:
6
Peritonitis
Acute intestinal obstruction
Diarrhoea
Acute renal failure
Entero-cutaneous fistula
The serum electrolytes (mmol/l) of a patient are Na: 125, K: 6.1, Cl:
106, HCO3, 20. The blood urea is 10 mmol/l/ and the pH 7.2. The
diagnosis is:
Severe diarrhoea
Entero-cutaneous fistula
Renal failure
Acute intestinal obstruction
Diarrhoea and vomiting
Conditions that may lead to hypomagnesaemia include:
Confusion
Hyporeflexia
Muscular twitches
Vomiting
Rapid deep respiration
Which of the following has the same electrolyte composition as
plasma?
Gastric juice
Duodenal secretion
Bile
Pancreatic secretion
Ileal secretion
A 20-years old patient with acute peritonitis and dry tongue has
7
the following serum electrolytes (mmol/l): Na:140, K: 3.8, Cl:95,
HCO3, 25, blood urea 7.5. The interpretation is:
Naso-gastric aspiration
Losses from entero-cutaneous fistula
Losses from diarrhoea
Losses from vomiting not due to gastric outlet obstruction
Losses from peritonitis
Water requirement of infants is different from that of adults
because:
8
are about 900 ml and 72 mmol respectively
The daily energy requirement for homeostasis is equivalent to
150G.
of glucose
Muscle cramps
Hypotension
Convulsion
Rapid shallow breathing
Hyperkalaemia
About buffers:
3.5-4.5
4.5-5.5
5.5-6.5
6.5-7.5
7.5-8.5
Causes of respiratory acidosis include:
Decreased blood pH
PCO2 above 45 mmHg
9
Initial elevation of HCO3
Elevated total buffer base
Depressed serum potassium
Metabolic acidosis may be caused by:
In metabolic acidosis:
Peritonitis
Gastric outlet obstruction
Shock
Paralytic ileus
Biliary fistula
At the end of the second post operative day after partial
gastrectomy in a 40-year old man, his Intake-Output chart is as
follows:
Intake: IL Ringer’s lactate + 2L 5% Dextrose + Vits B and C
Output: Urine 750 ml, Nasogastric aspiration 1000 ml
For the next 24h, you may prescribe in addition to Vits B and C
10
2L Normal saline, 2L 5% Dextrose, 40 mmol KCL
Sodium : 90 mmol
Potassium 20 mmol
Chloride 80 mmol
Bicarbonate 30 mmol
Glucose 20G
Fluid 5:4:1 contains per litre:
Sodium bicarbonate 5g
Sodium chloride 4g
Potassium chloride 1g
Glucose 50g
The Ghanaian male of 60kg who:
ANSWERS
B, D 28. D
A 29.A
A, C, D 30.A, B, C, E
A 31. C
B, C 32. B, D, E
A, C 33. A, C
B, E 34. C
A, D 35. C, E
11
B, D 36. A, D
B, C, D 37. A, D
A, B, C, D, E 38. A, C
A, C 39. A, B, D
B, C, D 40. B, E
A, D 41. B, D
A, E 42. B
B 43. A, D, E
B, E 44. A, B
B, D 45. A, C, D, E
C 46. B, D
D 47. B
A, B, C, D 48. B, C
C 49. A, B, C,D, E
B, C 50. C
A, B, E 51. A, C
A
C
C
12
CHAPTER 11
BLOOD TRANSFUSION, HAEMOSTASIS AND ABNORMAL
HAEMOSTASIS
1. A blood donor should:
1
5. A patient who is having blood transfusion for the first time
complains of
fullness in the head, dyspnoea, constricting pain in the chest and
fever.
2
8. You will give:
A. Chloroquine injection
B. An antihistamine
C. An antibiotic
D. A diuretic, sodium bicarbonate and normal saline
E. Nothing
9. Mild jaundice developing about 5 days after uneventful blood
transfusion
may be due to:
Haemolysis of old donor red cells
Production of antibodies which were too low to be detected at the
time
of cross-marching
Early viral hepatitis
ABO antigen-antibody incompatibility
Sepaticaemia
10. Which of the following cannot be transmitted by blood stored for
more
than 48h?
Viral hepatitis
Syphilis
Malaria
Trypanosomiasis
Infectious mononucleosis
11. Bleeding following mismatched blood transfusion is due to the
release of:
3
A. Vasoactive substances
B. Adenosine Diphosphate
C. Free haemoglobin
D. Platelet factor 3
E. 5, hydroxytryptamine
4
Hypocalcaemia
15. Red blood cells in banked blood:
A. Swell by about 20 per cent
B. Have a normal concentration of ATP
C. Have a diminished concentration of 2, diphosphoglycerate
D. Have a normal life-span
5
membrane
D. Prostacyclin synthesized in the block vessel wall from arachidonic
acid
19. Which of the following is/are involved in the conversion of
soluble fibrin
monomer (Factor 1a to insoluble fibrin polymer (Factor 1b)?
Thrombin
Factor V
Calcium ions
Factor VII
Factor XIII
6
A. Fibrinogen degradation products
B. Prostacyclin
C. Antithrombin III
D. First component of complement
E. Adenosine diphosphate
23. Fibrinogen degradation products:
A. Result from lysis of fibrin
B. Stimulate thrombin
C. Form non-clotting complexes with fibrin monomers
D. Stimulate fibrin polymerization
24. Which of the following opposes the action of thromboxane A2?
A. Plasma
B. Thrombin
C. Prostacyclin
D. Antiplasmin
E.Thromboplastin
7
27. Platelet aggregation is impaired by:
A. Cyclophosphamide
B. Aspirin
C. Quinidine
D. Phenacetin
E. Chloramphenicol
28. Bleeding in uraemia is caused by:
A. Deficient number of platelets
B. Defective release of platelet factor 3 (pf3)
C. Diminish content of PF3
D. Inhibition of platelet aggregation
E. Decreased activity of factor VIII
29. In haemophilia:
A. Factor VII activity is less than 30 per cent of normal
B. The disease is transmitted by a sex-lined dominant gene from a
normal male carrier to male off springs
C. The partial thromboplastin time is prolonged
D. The bleeding and prothrombin times are prolonged
30. Obstructive jaundice leads to depression of:
A. Factor II
B. Factor V
C. Factor VII
D. Factor IX
E. Factor X
31. Disseminated intravascular coagulation may occur in:
A. Amniotic fluid embolism
8
B. Retained dead foetus
C. Mismatched blood transfusion
D. Hypovolaemic shock
E. Viperine venom
32. In disseminated intravascular coagulation:
A. Fibrinogen level is usually below 1.0 g/ litre
B. The bleeding time is normal
C. The clotting time is prolonged
D. Platelet count is depressed
E Factor V is normal but Factor VIII is depressed
9
35. Diseases that may be transmitted by blood transfusion include:
A. Cytomegalic inclusion disease
B. Toxoplasmosis
C. Brucellosis
D. Acquired Immune Deficiency Syndrome
E. Amoebiasis
36. Use of whole blood for transfusion in Ghana is justified in:
A. Sudden loss of 30% or more blood volume
B. Chronic anaemia
C. Patients undergoing exchange transfusion
D. Twin delivery
E. Patients with pancytopenia
10
B. Stop the transfusion temporarily
C. Give antipyretics
D. Inform the blood bank
E. Give Hydrocortisone with subsequent transfusions
40. The following are immediate transfusion reactions:
A. ABO incompatibility
B. Post-transfusion thrombocytopenic purpura
C. Circulatory overload
D. Infectious mononucleosis
E. Air embolism
41. Concerning ABO incompatibility:
A. The mortality rate can be as high as 50%
B. It usually results from wrong identification of blood and recipient
C. It involves the haemolysis of recipient cells by donor antibodies
D. The shock may lead to oliguria
E. The recipient usually gets jaundiced within an hour
11
blood
within 24 hours, the following measures should be taken:
The blood should be warmed before transfusing
Intravenous potassium should be give with every second unit
With every litre of blood given, 10mls of 10% calcium gluconate
should be given
The patients Hb level should be checked every 4 hours
The patients acid-base and electrolytes should be checked
frequently
45. Methods of autologous transfusion include:
A. Optimal dosing with erythropoietin and iron
B. Preoperative blood donation
C. Hidden paid donation
D. Acute isovolaemic haemodilution
E. Intraoperative blood salvage
12
48. Activated Protein C inhibits activated factors:
A. VIII
B. II
C. X
D. V
E. IX
49. In DIC there is:
A. Thrombocytopenia
B. Lymphocytosis
C. Dysfibrinogenaemia
D. Shortened APTT
E. Increased D-dimer levels
13
CHAPTER 11
BLOOD TRANSFUSION, HAEMOSTASIS AND ABNORMAL
HAEMOSTASIS
1. A, D, E 38. A, B, C
2. D 39. B, C, D
3. A, D 40. A, C, E
4. A 41. A, B, D
5. C 42. B, C, E
6. C, E 43. A, B, C, D, E
7. C 44. A, C, E
8. B 45. B, D, E
9. A, B 46. A, C, D
14
10. B 47. A, D, E
11. B, D 48. A, D
12. A, B, C, D 49. A, E
13. B, C 50. A, C, D
14. A, B, C
15. A, C
16. A, C, D, E
17. C
18. A, C
19. A. C, E
20. A, C, D, E
21. A, B, C, D, E
22. B
23. A, C
24. C
25. E
26. A, B, C
27. B
28. B, C, D
29. A, C
30. A, C, D, E
31. A, B, C, D, E
32. A, C, D
33. A, B, C, D
34. A, C
35. A, B, C, D
36. A, C
37. B, D, E
15
CHAPTER 12
NUTRITION IN SURGERY
Proteins
Carbohydrates
Electrolytes
Water
Vitamins
Water
Sodium
Glucose
Amino acids
Potassium
Water
Sodium
Dextrose
Potassium
1
Amino acids
Glycine
Leucine
Valine
Phenylalamine
Alanine
Carbohydrates (C) fat (F) and protein (P) provide energy in the
following
percentages:
C F P
2
50 30 20
55 35 10
45 40 15
50 35 15
50 40 10
Fructose:
Does not require insulin for the initial stages of its metabolism
Sorbitol:
Is a sugar alcohol
Is converted to glucose
Xylitol:
Is converted to fructose-6-phosphate
3
May produce metabolic alkalosis
Alcohol:
Is quickly metabolized
Brain
Liver
Polymorphs
Skeletal muscle
Is hyperosmolar
of nitrogen?
4
20
25
30
35
40
Methionine
Glycine
Alanine
Phenylalanine
Proline
In intravenous nutrition:
5
Central vein catheterization is mandatory for the administration of
isotonic
every 72h
suggest:
Severe burns
Severe amoebiasis
Partial gastrectomy
6
Metabolic alkalosis
Pneumothorax
Anaemia
Hyponatraemia
Septicaemia
Over-hydration
Haemothorax
Rebound hypoglycaemia
Thrombosis
25-29.9 is obesity
30-35 is overweight
Glutamine
Glucose
Arginine
Nucleotides
7
Omega-3 fatty acids
Lactate
Fatty acid
Glycerol
Arginine
Ketones
Fat
Water
Sodium
Proteins
Glucose
Clotting studies
Serum calcium
Weight
Pneumonia
8
Wound dehiscence
Cerebrovascular accident
Reflux
Aspiration pneumonia
W P F M
65 15 15 5
60 15 20 8
55 15 25 5
60 18 15 7
50 25 15 10
9
A standard TPN regimen for an adult contains:
Vitamins A, B, C, D, K
Cheilosis
BMI 18.0kg/m2
10
CHAPTER 12
NUTRITION IN SURGERY
ANSWERS
A, B, C, D, E 29. D
A, B 30. A, B, C, D, E
A, B, C, D, E 31. A, B, D
A, C, E
C, E
D
B, C
A, C
A, B, C
A, B, C
A, C, D
A, C
C
A, D
11
A, C, D
B
B
A, B, E
A, C, D
B, C, E
A, B, C, D, E
A, C
A, C, D, E
A, C, D
B, C
A, C, D
A, B, E
A, B, C, D, E
12
CHAPTER 13
MANAGEMENT OF THE INJURED PATIENT
1
Reduction in cardiac output
Pulsus paradoxus
Pulsus alternans
Collapsing pulse
Small intestine
Spleen
Liver
Colon
Pancreas
In which of these injuries would the serum amylase level be raised
above normal?
Ruptured bladder
Fractured pelvis
Duodenal perforation
Rectus muscle haematoma
Ruptured spleen
In which of these injuries would the serum amylase level be raised
above normal?
Duodenal rupture
Gastric perforation
Pancreatic injury
Intestinal perforation
Liver injury
Which of the following radiological features is/are often seen in
the patient with ruptured spleen?
2
Pneumoperitoneum
A man of 40 who sustained a crushing injury when his V.W car
was in collision with a minibus presented in Casualty with severe
upper abdominal pain and dyspnoea. On examination he was
anxious, not anaemic with a pulse of 96/min and a BP of
110/75mmHg. His chest was clear, he was tender in the right
hypochondrium and his liver was palpable and tender. The bowel
sounds were normal and rectal examination was unremarkable.
3
Four quadrant tap or peritoneal lavage
Plain X-ray of the abdomen
Which of the following may be encountered as complications of
management of hepatic injuries?
Atelectasis
Empyema
Purulent intraperitoneal collection
Secondary haemorrhage
Thrombocytopaenic purpura
4
Department 24h complaining of severe lower abdominal pain. He
had passed urine with some difficulty initially but denied
haematuria. He was pale and anxious and an enlarged tender
bladder was felt in the lower abdomen; a small blood clot was
seen at the tip of the penis and no urinary extravasation was seen,
the perineum was normal. No pelvic fractures were detected.
5
Subaponeurotic
Subcutaneous
Subperiosteal
Intracutaneous
Extradural
Scalp haematoma should be treated:
By needle aspiration
By incision and evacuation
Conservatively and should settle in 1-10 weeks
By exhibition of broad spectrum antibiotics
By weekly injection of hyaluronidase
Which of these features may be regarded as frequent modes of
presentation of chronic subdural haematoma?
Headache
Vomiting
Fluctuating level of consciousness
Psychotic changes
Pseudo bulbar palsy
6
Optic nerve damage
Pontine injury
Extradural haematoma
Damage to the optic chiasmma
Indication(s) for elevation of a closed, depressed fracture include:
Radiographic evidence of indriven bones spicules
Evidence of cerebral compression
Depression causing disfigurement, especially in the forehead
Depression more than 4mm in functionally important areas of the
cortex
Depression in a child without evidence of compression.
Noted complications of head injuries include:
Subarachnoid haemorrhage
Meningitis
Cerebral abscess
Fat embolism
Hypernatraemia and hypernatraemia
Chronic subdural haematoma:
Is commonly caused by trauma
Commonly presents with mental changes
Is treated by craniotomy and evacuation
Haematoma enlarges because of defective haemostasis
May be confused with cerebrovascular accident
7
An extradural haematoma
Hypocarbia
The most common cause of cardiorespiratory failure in a spinal
cord injury patient is:
8
extended
Early endotrachael intubation of the severaly injured
Scooping out vomited gastric contents with gauze or handkerchief
Strapping an unstable segment of chest wall with a pad
Inserting a needle in the second intercostal space of the patient with
tension pneumothorax
At the road side practicable respiratory resuscitative measures
should include:
Grasping the tongue between thumb and index finger and drawing
it forwards in the unconscious patient.
Maintaining patency of the airway by working the angles of the
mandible with the thumb
Fixing a clean cloth over any open chest wound
Lying the patient on the paradoxically moving segment of chest wall
during transportation
Aspiration of the chest of the patient mildly dyspnoeic with
haemothorax
In the transportation of the injured person to hospital:
The ideal means is a ground or air ambulance
Speed of transit often determines the prognosis
The position of choice in transit is supine with the head to the side
The unconscious patient should have endotracheal intubation
All resuscitatory effort should continue unabated in transit
Emergency or crashroom care of the injured person:
Aims at consolidating what has been achieved at the road side
Emphasizes control of life threatening asphyxia
Ensures control of continuing external bleeding by means of
haemostats and ligatures
Should ensure that the patient is made fit for any exploratory
procedure necessary
Includes careful monitoring of the patient’s vital signs, and his
peripheral perfusion
9
Due consideration for tracheostomy in patients with respiratory
difficulties early
Transfer of the patient with paradoxically moving chest to
management by intermittent positive pressure ventilation
In the emergency or cashroom, respiratory resuscitative
measures should include:
Suctioning of the trachea of all severely ill patients
Endotracheal intubation of all unconscious patients
Nasotracheal as opposed to endotracheal intubation of all patients
with obstructed airway
Control of the paradoxically moving chest by strapping
Relief of tension pneumothorax by passage of intercostal tube drain
through second intercostal space.
Emergency or crashroom management of the injured patient
should ensure:
Administration of enough blood and fluid to prevent shock
Accurate monitoring of the patient’s vital signs
Tetanus prophylaxis through toxoid administration in open wounds
or burns
Administration of a bolus dose of a broad spectrum bacteriocidal
antibiotic in all cases of abdominal trauma
Thorough investigation for other causes of unconsciousness
besides head injury
Emergency or crashroom management of the injured patient
should ensure:
Rapid infusion of blood and fluids to bring the blood pressure within
normal limits
Careful monitoring of the central venous pressure and hourly urine
output as best indices of tissue perfusion
Tetanus prophylaxis through antitetanus serum administration in
open wounds and burns
Administration of bolus dose of a broad spectrum bacteriocidal
antibiotics in all cases of thoracic trauma
Administration of bolus dose of a broad spectrum bacteriocidal
antibiotics in all cases of significant head injury
In the definitive care of the patient with multiple injuries:
A team work approach is rewarding
In general, priority is determined by the rapidity with which injuries
affect cardio-respiratory function
Judicious use of abdominal paracentesis and lavage expedites the
diagnosis of latent injuries
Orthopaedic injuries are usually kept splinted and treated on a
semi-emergency basis.
Hand injuries are deserving of early attention taking precedence
10
over other closed fractures.
Judicious use of FAST enhances early diagnosis
In the definitive care of the patient with multiple injuries:
The work of the team of experts should be co-ordinated by an
experienced general surgeon
Tension pneumothorax or open sucking wounds should take
precedence over head injuries
Use of abdominal paracentesis and lavage makes no difference to
timing of diagnosis
Orthopaedic injuries should always be managed under the same
anaesthetic with abdominal injuries
Contaminated wounds or compound fractures should be dealt with
within the shortest possible time.
Thoracic trauma:
Account for 25 per cent of deaths following automobile accidents
Produces derangement in respiratory movements with
hypoventilation and respiratory acidosis
Should be managed by urgent attention to the airway
May demand attention to open sucking wounds, pneumothorax and
haemothorax
Cannot be adequately managed without chest X-ray.
A rib fracture:
Occurs at point of impact or at its weakest point which is the angle
If uncomplicated is not a serious problem except in the elderly in
whom respiratory acidosis could supervene
May be complicated by pneumothorax and surgical emphysema
May in the elderly lead to lung collapse, consolidation, and
respiratory failure
Should be treated by intercostals nerve block and active
physiotherapy
Multiple rib fractures:
May produce a flail chest
May produce a “stove” in chest
May through paradoxical chest movements produce a mediastinal
flutter
Usually increases intrapulmonary shunting and thereby produce
dyspnoea, tac-typnoea and even cyanosis
If causing significant paradoxical movements need stabilization by
intermittent positive pressure ventilation
Ruptured diaphragm:
Usually results from blunt trauma or crush injuries
Usually occurs on the left side
Is often indicated by appearance of intra-abdominal structures in
11
the left chest
Presents with shoulder tip pain as a frequent feature
Is often attended by high incidence of strangulation of herniated
bowel
Ruptured diaphragm:
Usually occurs from vibration injuries
Occurs with equal frequency on both sides
Is often attended by severe shock
Nearly always presents with shoulder tip pain
Is best seen on a lateral chest X-ray
Haemothorax:
Results from bleeding originating from the systemic as well as
pulmonary circulation
Causes collapse of underlying lung
Eventually leads to a reduction of cardiac output
Can be reliably diagnosed on clinical grounds
Should be so treated as to achieve complete and sustained re-
expansion of the lung
Rupture of a major airway:
May result from blunt trauma
Usually causes dyspnoea associated with haemoptysis
Is an important cause for tension pneumothorax
Should be treated by early thoracotomy and repair of the tear in the
passages
May lead to broncho-stenosis, infection and lung tissue destruction
Bullet wounds of the abdomen:
Usually call for exploratory laparotomy
Are often associated with chest injuries
Usually show a small entry point but considerable exit damage
From a shot gun at close range is regarded as particularly
devastating
Having a better prognosis compared to stab wounds
Diagnosis of blunt abdominal injuries:
Is frequently made difficult because of clouding of consciousness
from associated head injuries or alcoholism
Is much helped by information on mechanism of injury
Is facilitated by a reliable record of the vital signs during
observation of the patient
Should be entertained in event of a rising white cell count,
particularly levels above 15 x 10-3 per dl
Affecting the pancreas, stomach, duodenum, intestine should be
12
suspected if serum amylase levels are elevated and sustained.
Diagnostic abdominal paracentesis in abdominal trauma:
Is most useful in patients who are comatose from associated head
injuries or alcoholic intoxication
Has a diagnostic accuracy of 85 per cent
Is usually productive of blood that does not clot on standing
Has the practical value of shortening the period of observation for
patients with occult injuries
Should avoid areas where bowel could be attached to the parieties.
Peritoneal lavage in abdominal trauma:
Represents an improvement on the accuracy of diagnostic
paracentesis
Is performed through a low midline incision under local anaesthesia
Is best evaluated by a microscopic and chemical analysis of the
perfusate
Suffers from the disadvantage of enhanced sensitivity
May be positive in many cases of retro-peritoneal haematoma not
requiring surgical exploration
Delayed rupture of the spleen:
More often represents only a delayed recognition of splenic injury
May result from digestion of initial clot by enzyme released by
concomitant damage to tail of the pancreas
May be diagnosed earlier by means of selective celiac angiography
in suspicious cases
Should be treated by splenectomy
Presents a more formidable operative problem than primary rupture
Ruptures of the liver:
Are usually the result of crush injuries to the lower chest and upper
abdomen
May present as subcapsular haematoma
Should be explored on suspicion
If treated by resection should have T-tube drainage of the
extrahepatic biliary tree
Are associated with thoracic injuries in nearly 50 per cent of cases.
Ruptures of the liver:
May follow vibratory forces to the abdomen
If significant frequently perish at the road side
Should be treated by simple drainage alone if simple and not
actively bleeding at operation
If survived leave no stigmata of hepatic insufficiency
Are associated with head injuries in nearly 50 per cent of cases.
Pancreatic injury:
13
Is more often inflicted by penetrating trauma
Is often associated with stomach, liver and duodenal lesions
Is diagnosed when high serum amylase levels are accompanied by
peritoneal signs
Need exploration on suspicion
If explored should be adequately drained
The duodenum:
Is most frequently injured in its second part
Is more frequently injured by penetrating trauma
The site of injury is often detected late because signs are frequently
in abeyance
If suspected to be injured should be urgently explored
The site of injury is liable to fistula formation
Colonic injuries:
Usually result from blunt injuries following road traffic accidents,
falls and impalement
May be masked in delayed injuries resulting from confusions or
ischaemia
Should be explored on suspicion by laparotomy
If simple and linear may be treated by suture in two layers
If extraperitoneal should be treated by exteriorization
Colonic injuries:
May be produced by foreign bodies which have passed through the
alimentary canal
May be detected by careful physical, rectal and sigmoidoscopic
examination
Should have a pre-operative antibiotic cover, e.g. ampicillin, 3rd
generation cephalosporins
If extensive should be treated by resection and primary
anastomosis
Having an invariably poor prognosis
Retroperitoneal haematoma:
Most commonly results from blunt abdominal trauma
Presents considerable diagnostic difficulty
Is most commonly associated with pelvic fractures
Gives rise to a positive peritoneal tap in 50 per cent of cases
Gives rise to a positive peritoneal tap in 10 per cent of cases
Retroperitoneal haematoma:
Most commonly results from penetrating abdominal trauma
Should be suspected in patients showing hypotension after
abdominal trauma but no overt abdominal signs or external
14
haemorrhage
When expanding indicates associated injury of the great vessels
Is suggested by tender mass in the flanks
Should be explored when adjacent to pelvic fractures
Renal injuries:
Occur most commonly in road traffic accidents (35 per cent of such
cases)
May be associated with injuries to the lumbar muscles and fractures
of the spine
Should be suspected where loin pain follows abdominal trauma
May present with a renal mass representing extravasation of urine
In 80 per cent of cases respond to conservative measures
Ureteric injuries:
Commoly accompany renal injuries
If extraperitoneal may produce pelvic or loin swelling
May present as pain in the flanks or lower abdomen following
crushing trauma
Show on isotopic renogram as increased counts on the side of the
ligated or damaged ureter
Presenting as anuria should be urgently explored and treated by
bilateral ureter-onoecystostomy
Urteric injuries:
May follow trauma producing hyperextension of the spine
May produce urinary vaginal fistula
May show urographically as ureteric dilatation, hydronephrosis or
extravasation of contrast
May how urographically as non-functioning kidney of affected side
Presenting late should need management for uraemia and infection
prior to surgical repair
Intraperitoneal rupture of the bladder:
May be caused by road traffic accidents and contact sport
Is usually follow trauma to lower abdomen in a patient with a full
bladder
Is suggested by a history of anuria, after trauma with few drops of
blood stained urine and ascites and peritonitis
Can be confirmed by retrograde cystogram
Should be treated by early repair of the vesical tear and bladder
drainage by urethral or susprapublic catheter.
Extraperctoneal rupture of the bladder:
May complicate pelvic fractures
Usually follow lower abdominal injury in a patient with empty
bladder
15
Is suggested by a tender suprapubic mass with extravasation of
urine after lower abdominal trauma
Peritonitis is usual clinical presentation.
Should be treated by preliminary supra-pubic cystostomy and
delayed accurate repair of bladder tear
Injuries to the membranous urethra:
May be “complete or “partial”
Usually occur just beyond the apex of the prostate gland
Usually lead to extravasation of urine on to the perineum
Should be suspected in the patient who after abdominal trauma has
urethral bleeding and difficulty in micturating
Should be treated in the early lesions by urethral catheterization
under aseptic conditions.
Injuries to the membranous urethra:
May co-exist with vesical injuries
Is seen in 10 per cent of pelvic fractures
Seldom lead to extravasation of urine on to the perineum or the
groin
Should be suspected in a patient who develops tender palpable
bladder with blood at the tip of the penis after abdominal trauma
If overlooked for more than 48 h should be treated by suprapubic
cystotomy only in the first instance.
16
observation
May contribute to the decision to admit a head injury for observation
Extradural haematoma:
Is a haematoma between the skull and the dura
Is usually found in the temporal region
Usually occurs in children without a skull fracture
Is attended by early pupillary constriction on the side of the lesion
followed by dilatation
Should be treated by urgent evacuation of haematoma and arrest of
bleeding through exploratory burr holes
Extradural haematoma:
Is a haematoma between the bony skull and its periosteum
May occasionally be seen in the parietal or frontal region
Is not always attended by loss of consciousness
May be marked by a slowing pulse and a rising blood pressure
May be complicated by epilepsy and a rising blood pressure.
May be complicated by epilepsy in a third of survivors
Subdural haemorrhage:
Is acute if it occurs within 48h and usually complicates severe head
injuries
In the acute form may be difficult to distinguish from an extradural
haemorrhage
May occasionally result from rupture of an aneurysm or angioma
Often presents with fluctuation in level of consciousness
Shows diagnostic changes on carotid angiography (postero-anterior
views)
Subdural haemorrhage:
Is subacute when it occurs between 2-14 days after injury
Increases in size by repeated haemorrhages or osmostic absorption
of fluid.
In the chronic form may be associated with a history of head trauma
in about half the patients
Not uncommoly presents as a psychosis leading to admission to a
mental hospital
Should be treated by exploratory burr holes in the temporal, parietal
and frontal positions.
The patient that is unconscious with a head injury:
Should be positioned on his side with a slight head down tilt
Should be so positioned to ensure a clear airway which is checked
by regular suctioning
Should have adequate skin care to forestall bed sores
17
Should receive judicious infusion of intravenous fluids in the first
48h.
May benefit from a course of dexamethzone 10mg I/V, then 5mg
i/m 6 hourly for 4 days.
Fractures of the base of the skull:
Classically present as C.S.F. leakage from the nose or ear
Should have any fluid leakage from nose or ear tested for sugar
Should be treated with bed rest and systemic antibiotics
If not responding to conservative measures should be treated with
repair of the dural tear by a fascial patch
May be responsible for intracranial aeroceles
Cerebreal oedema:
Is common complication of head trauma
Clinically mimics intracranial haematoma
Is much aggravated by hypoxia
May be treated by infusion of 20 per cent mannitol (250-500ml)
administered over about 20 minutes
Is attended by a high incidence of late post-traumatic epilepsy.
Cerebral oedema:
Is a constant threat to the life of the victim of head injury
Is confirmed at exploratory burr holes when the brain is soft,
swollen and contused
Is often aggravated by associated chest disease or injury
Should be treated by a regime including restriction of fluid to 2L and
sodium 150mmol in 24h
May be complicated in the first few days by epilept form fits
Post-traumatic epilepsy:
Is recognized as early if it occurs within one week of injury
If early takes the form of a focal motor attack
Of the late type has an incidence of 5 per cent but tends to be
persistent
Should be treated prophylactically, identifying all patients with a
predisposing type of injury
If early may be treated with intramuscular diazepam 10mg
Post-traumatic epilepsy:
Is recognized as late if it occurs after one week after injury
Of the early variety has an incidence of 5 per cent of non-missile
injuries
Of the late type has an incidence of 15 per cent and tends to persist
18
Should be treated with phenobarbitone 30 mg t.i.d. in adults and
children over 12 years
Has a worse prognosis than idiopathic epilepsy
Arterial injuries:
I f of the contusion type are more likely to follow fractures and
dislocation of joints
Should be suspected when paralysis, pain, paraesthesiae and
pallor are noted in a limb after injury.
Should be treated by early exploration after seeing to fractures and
dislocations
Affecting vessels less than 5mm in diameter are treated by ligation
rather than repair
Should after exploration be managed by 100 elevation of the
affected limb
Features to be observed in the Glasgow Coma Scale include:
Eye opening
Corneal reflex
Pupillary reaction to light
Motor response and patellar reflex
Verbal response
In the Glasgow Coma Scale a patient with eye opening to pain,
incomprehensible verbal response, and forearm flexion to pain
has a score of:
10
9
8
7
6
19
Take a light diet
Take aspirin or paracetamol if he has headache
Take antacids to prevent acute gastric erosions
Return immediately to hospital if a member of the family is anxious
about him
If a patient with minor head injury without loss of consciousness
is sent home and not hospitalized, his relations should be
instructed to look out for:
Vomiting
Frequency of urine
Abnormal behavior or restlessness
Weakness of an arm or leg
Increasing sleepiness
Primary or impact brain damage produces:
Intradural haematoma
Cerebral confusion
Brain swelling
Diffuse axonal injury in the white matter
Subarachnoid haemorrhage
“Minor” head injuries not requiring hospitalization include:
Small scalp laceration without loss of consciousness
Simple fracture of the cranial vault without loss of consciousness
Concussion
Minor contusion of scalp with post traumatic amnesia of less than 5
minutes.
Fracture base of skull without C.S.F. otorrhoea.
20
CHAPTER 13
MANAGEMENT OF THE INJURED PATIENT
ANSWERS
A, B, C, D 39. A, B, C 77. A, D,
E
A, B, C, D, E 40. A, B, C, D 78. A, B,
C, D
A, B, C, D 41. A, C, D, E 79. A, B,
D, E
C 42. A, B, C, D 80. B, C,
D, E
A, B, C 43. A, B, C, E 81. A, B,
C, D, E
A, B, C, D 44. A, B, C, D, E 82. B, C,
D, E
A 45. A, B, C, D, E 83. A, B,
C, D, E
C 46. E 84. A, B,
C, D, E
A, B, C, D 47. A, B, C, D, E 85. A, B,
C, D, E
B 48. B, D 86. A, B,
C, D, E
C 49. A, B, C, D, E, F 87. A, B,
C, D
A, C 50. A, B, E 88. A, C,
D, E
E 51. A, B, C, D, E 89. A, B,
C, D, E
A 52. A, B, C, D, E 90. A, B,
D
A, B, C, D 53. A, B, C, D, E 91. A,B,
C, D, E
A, B, C, D 54. A, B, C, D, E 92. A, E
A, B, C 55. C, D, E 93. D
A, B, C, D, E 56. A, B, C, D, E 94. B, E
A, B, C, D, E 57. A, B, C, D, E 95. A, C,
D, E
C 58. A, B, C, D 96. B, D
21
A 59. A, B, C, D, E 97. A
B 60. A, B, C, D, E
A 61. A, B, C, D, E
A, B, C, D 62. A, B, C, D, E
C 63. A, B, C, E
A, B, C, D 64. A, B, C, D
C 65. A, B, C, D, E
C 66. A, B, C, D, E
A, B, C, D 67. A, B, C, D
A, B, C, D, E 68. A, B, C, D
A, B, C, D, E 69. A, B, C, D
A, B, D, E 70. B, C, D
A, C, D, E 71. A, B, C, D, E
C, D, E 72. B, C, D, E
A, B, C, D 73. A, B, C, D, E
A 74. A, B, C, D, E
B, D 75. A, B, C
D, E 76. A, B, D
22
CHAPTER 14
BURNS
A Burn:
Is coagulative destruction of skin which may be caused by hot water
Occurs most commonly in children
Is pathologically different from scald
Injury depends on the temperature of the heat source but not on the
duration of exposure of the tissues to such temperature
In the adult may be due to RTA
In deep partial thickness burns destruction of the following occur:
Lymph vessels
The hair follicles and sebaceous glands
Sweat glands
Red cells
Capillaries
Mediators released after burns include:
Histamine
Cyclo-oxygenase pathway products
Serotonin
Prostaglandins
Thyroxine
Cold water immersion after thermal injury:
Increases the risk of infection
Reduces pain after partial thickness burns
Can result in hypothermia if applied to large burns
Has been reported to stabilize mast cells
May decrease oedema if applied immediately
The protein content of oedema fluid in burns may be as much as
(g/1):
60
20
30
40
50
The electrolyte composition of oedema fluid in burns:
Has a higher sodium concentration than plasma
Has a lower potassium concentration than plasma
Has a higher bicarbonate concentration than plasma
1
Has a lower chloride concentration than plasma
Is the same as that of plasma
In burns:
The maximum oedema fluid obtainable is about 10% of body
weight or 50% of total E.C.F
There is initial vasodilatation followed by vasoconstriction
The rate of fluid exudation from the capillaries is highest in the first
6h. and falls in 48h.
Increased capillary permeability may occur even in unburnt areas
Immediate charring of the skin lessens external and subcutaneous
fluid loss
Anaemia in burns may be caused by:
Thrombosis
Increased red cell fragility
Changes of dressings
Bone marrow depression
Skin grafting
In burns:
There is depression of cellular and immunological mechanisms
Leucocytes cannot phagocytose bacteria normally
There is depression of lysosomes
IgG is not affected
Transfer of leucocytes and antibodies to sites of bacterial infection
is rapid and not depressed
In burns:
Renal failure is commonly caused by toxic substances produced in
the burnt skin
The urine may occasionally be port-wine
Uraemia is always associated with oliguria
There may be necrosis of the distal convoluted tubules
The renal vessels are dilated
Organisms that may infect a burn in the first 24h include:
Proteus
Streptococcus
Pseudomonas
2
Esch. Coli
Staphylococcus
Predominant organisms in a scald wound by seven days include:
Staphylococcus
Pseudomonas
Pneumococcus
Clostridium tetani
Streptococcus
3
Face
Neck
Entire trunk
Perineum
Axilla
Curling’s ulcer:
Occurs only in the stomach and duodenum
Occurs only in severe burns
Is often complicated by bleeding
May be prevented by the administration of antacids or cimetidine to
severely burnt patients in the first three weeks
Is best treated by partial gastrectomy or vagotomy and drainage
4
burns
of the face, right upper limb and anterior part of the trunk
following a fire
in is bedroom at 12 midnight. He is brought to the ‘Casuality’ at
2.00 a.m.
Your first concern will be to:
Check his pulse and blood pressure and administer morphine.
Remove his clothes and determine the extent and depth of his burn
Check the rate of his breathing
Find out if the airway is clear
See if there is singeing of his nasal hair or soot in the nostril
Examination of the burnt area shows that there are blisters, areas
of erythema and other areas of skin which are all sensitive to pin
prick.
The burn is:
Superficial partial thickness
Deep partial thickness
Full thickness and superficial partial thickness
Partial thickness (superficial and deep)
Full thickness
The burn is estimated at 30% of his body surface. The total fluid
requirement (in litres) in the first 24h is about:
5.5
6
6.5
7.2
7.5
The fluids will consist of:
2L 5 per cent dextrose, IL blood and the rest as Ringer’s lactate
Ringer’s lactate
5
2L blood and the rest as ringer’s lactate
2L 5 per cent dextrose and the rest as Ringer’s lactate
IL 5 per cent dextrose; 2L dextran 70 and the rest as Ringer’s
lactate
Half the fluids should be given by:
6a.m
8a.m
10a.m
12noon
2p.m
Initial investigations will include:
Haematocrit
Blood group
Serum electrolytes and blood urea
Culture of the burnt skin
White cell count and differential
The antibiotic to administer at this stage is:
Chloramphenicol
Cloxacillin or penicillin
Gentamicin
Oxytetracycline
Cephaloridine
The most important parameter to monitor is:
Quarter-hourly pulse and blood pressure
Central venous pressure
Filling of peripheral veins
Hourly urinary output
Skin temperature and orientation
After cleaning the burn wounds with one per cent centrimide you
will apply:
Terracortril spray daily
0.5% silver nitrate dressing and add more silver nitrate every 3h
6
Silver sulphadiazine cream on alternate days without dressing
Mafenide creame twice daily
Povidone-iodine daily
The fluid requirement (in litres) in the second day is
approximately:
4
4.5
5
5.5
6
On the second day the urine is found to be port-wine in colour.
You will after examining the urine:
Restrict fluid intake
Order an urgent I.V.P.
Give blood
Give 10% mannitol
Give sodium bicarbonate
On the 8th day he complains of some pain in the wound, anorexia
and generally being unwell. His temperature is 38.50C and the skin
around the discharging wound looks reddened.
The clinical diagnosis is:
Cellulitis
Lymphangitis
Septicaemia
Burn wound sepsis
Necrosis of the burn
Effects of electrical injuries include:
Cardiac or respiratory arrest
Ventricular fibrillation
Auricular fibrillation
Rupture of blood vessels
Thrombosis of vessels
Late complications of electrical burn injuries include:
Impotence
Cataract
Epilepsy
Intractable headache
Abnormal gait
7
In electrical injuries:
8
102
103
104
105
106
9
Inflammable liquids should not be stored in the home
Epileptics should be banned from getting near fires
In electrical burn:
Extent of injury may be difficult to assess
In the presence of myoglobinuria IV lasix in indicated
Infusion of IV fluids must be at the rate to increase urine output to
above
50 mls/hr
Excision of necrotic muscles is indicated 48hrs after diagnosis
Silver sulphadiazine is contraindicated in this type of burn.
10
CHAPTER 14
BURNS
ANSWER
B, E 35. A, B, C, D, E
A, B 36. B, D, E
A, B, C, D 37. B
B, C, D, E 38. D
E 39. A, B, D, E
E 40. A, C, E
A, D 41. D
A, B, C, D, E 42. C, D
A, C 43. C, D, E
B, D 44. A, C, D, E
B, E 45. B, C, E
B 46. B, C, E
A, B, E 47. A, C
A, E 48. A, B, C, D
A, C 49. A, C, D, E
A, E 50. C, D
11
A, B, D
C, D
C
B, C, E
A, B, C, D, E
D
D
C
D
B
A, B, C
B
D
C
E
D, E
D
A, B, D, E
12
CHAPTER 15
Chest X-ray
Stool R/E
Drug therapy
Concurrent disease
Cold
A history of asthma
A haemoglobin of 10g/dl
1
Chest X-ray
E. C. G.
Airway obstruction
Respiratory infection
Wound infection
Have his blood sugar done before and after the operation
2
if it is not corrected before operation?
Hyponatraemia
Hypochloraemia
Hypokalaemia
Dehydration
Anaemia
With SS or SC disease is 3
Who is moribund and is not expected to live 24h with or without surgery is
6
A vein at the back of the hand is always preferable to one at the forearm
for setting up a drip
3
If the arm is not used for infusion the hand may be placed under the
buttock
There is no need for any measures if the patient is longer than the table
The tidal volume is decreased by the prone position but not by the steep
Trendelenburg position
Venous bleeding is less and the intracranial pressure low in the sitting
position
In the prone position a firm pillow must be placed under the shoulders and
4
another under the abdomen
The cause of a rise or fall of more than 15mmHg from the resting blood
pressure should be found
The colorimetric method of estimating blood loss can be done during the
operation
Oxgen given should be 50 per cent if the haemoglobin is less than 8g/dl
Vagal inhibition
Anaesthetic agents
5
Results in cessation of respiration and a fast heart if the heart beat can be
heard
Hyponatraemia
Myocardial infarction
Hyperventilation
Extended head
Hypercapnia
6
The most likely clinical diagnosis is:
Bronchopneumonia
Collapse of a lung
Asthma
Exudative pneumonitis
Intubation and suction of the trachea and bronchi and irrigation with small
amounts of saline
Administration of digoxin
Four-hourly temperature
Intake-output chart
7
unconsciousness:
The chin should be supported with the fingers and the head extended
An endotrachael tube should not be left in situ until the patient recovers as
it is most uncomfortable
Post-operative hypoxaemia:
Increases with age and does not occur after operations which do not
interfere with respiratory movements
Oxygen administration:
8
The incidence of post-operative vomiting is influenced by:
Duration of operation
Aspiration of vomitus
Myopathy
9
Administration of morphine
Bronchoscopy
Oxygen theraphy
Death
Cardiac arrest
Myocardial infarction
Respiratory failure
Cerebrovascular accident
10
Shock
Aspiration of vomitus
Hyperextend the bead, open the mouth, pull out the tongue and apply
suction if necessary
Apply a face mark with the head still extended and give 100% oxygen by
manual compression of a breathing bag such as ambu bag
Administer nikethamide I. V
Take blood for urgent Hb, serum electrolytes, PO2 , PCO2 and pH
Fifteen minutes after the diagnosis the patient is still unconscious, you
will:
11
Continue external cardiac massage
Digoxin
Lignocaine hydrochloride
Magnesium sulphate
Sodium bicarbonate
Adrenaline
Naloxone
Isoprenaline
Calcium chloride
Propranolol
Amiodarone
The heels of the hand may be placed over the sternum or sternum and
adjacent ribs
12
The patient should be supine and on an ordinary bed
Fractured ribs
Blood pressure
Level of consciousness
Pyrexia
Epilepsy
Hypocalcaemia
Hyponatraemia
13
Water overload
Sclerema:
Atelecasis:
Predisposes to bronchopneumonia
14
Two days after sigmoid colectomy, a 50-year old man develops pyrexia,
rapid shallow breathing, cyanosis, cough and pain in the left side of his
chest. On examination, respiratory movements are diminished and
percussion is dull in the left lower chest. Breath sounds are diminished on
that side.
Pulmonary embolus
Bronchio pneumonia
Pulmonary atelectasis
Tracheo-bronchitis
Aspiration pneumonia
Raised diaphragm
Pulmonary embolism:
15
May mimic pneumonia or myocardial infarction
Morphine
Atropine
Sodium bicarbonate
Urokinase
Streptokinase
Impending death
Persistent hypotension
Persistent hypoxia
Retention of urine
Distended stomach
Peritonitis
16
Failure to pass urine 12 hours postoperatively in spite of adequate fluid
therapy.
Dehydration
It is found that the blood pressure dropped to 80/60 mmHg for about 30
minutes during the night. The intravenous fluid administered during the
previous 24 h was 3 litres and the nasogastric aspiration was 1.5 litres.
Clinically the blood pressure is now 120/80Hg and the skin is dry and
warm.
Acute glomerulonephritis
17
mOsm/L, red cells, casts and albumen present, urea 140 mmol/L, sodium
70mmol/L The blood urea is 10 mmol/L.
Acute glomerulo-nephritis
4500ml of crystalloids
1L of crystalloids
Paralytic ileus
Gastric dilatation
Uraemia
18
Enema saponis
Urgent laparotomy
Administration of antibiotics
Enterocolitis:
Wound infection:
19
Occurs most commonly on the 7th post-operative day
Malignancy
Uraemia
Liver disease
Obesity
Obesity
Venous stasis
Age
20
Post-operative changes in the coagulating factors
Heparin:
Is antithrombin
Is antiprothrombin
Is antithromboplastin
CHAPTER 15
B, D
A, B, D, E
A
B
A, B, C, E
B, D
C
21
D
B, E
C
C, D
B, D
B
B, C, E
B, C, E
B, E
A, B, D
B, C, E
D
B
A, B, D, E
C, E
A, D
A, C, E
A, B, C, D, E
E
B
A, B, C, E
A, B, C, D
B
A, B, E
22
C, D
C
A, C
B, D, E
B, C, E
B, E
A, B
C, D, E
B, C, E
A, C, E
B, C, E
A, C, E
B, C
A, C, D
C, D
A, B, C, D, E
B, C, D, E
B, D, E
B,D
A
C
B
C
D
B, C
23
C, D
C
D
A, B, D, E
A, C, E
D
C, D
A, B, C
24
CHAPTER 16
Keloid:
Keloid:
Excision
1
None of the above
A sebaceous cyst:
Dermoid cyst:
A ganglion:
Is usually unilocular
2
Is best treated by aspiration of its contents and injection of
hydrocortisone sclerosant
Varruca vulgaris:
A 25-year old man has two swellings over the right greater trochanter.
The swellings are firm, mobile, circumscribed, non-tender,
subcutaneous and attached to the deep fascia.
Fibromata
Lipomata
Implanatation dermoids
Onchocercomata
Naevi(moles)
3
Should be excised as they may become malignant.
Bleeding
Ulceration
Hairiness
Increase in size
Increase in pigmentation
Desmoid tumour:
Haemangiomas:
4
The treatment of cavernous haemangioma at the age of five is:
Leave alone
Excision
Injectionof a sclerosant
Neurofibroma:
Lipoma:
5
and neck region in Caucasians
5-Fluouracil
Methotrexate
Cyclophosphamide
Cisplatin
Bleomycin
6
Occurs in the face in 90% of patients
Malignant melanoma:
Vincristine
7
Melphalan
Adriamycin
Actionmycin D
Dacarbazine
Dermatofirosarcoma:
Kaposi’s sarcoma:
8
Is most common in Jews, Italians and Africans and the highest
incidence in Africa is in Uganda
Bones
Intestines
Brain
Lungs
Liver
9
May be localized or generalized
Pathological fractures
Sclerosis
Osteoporosis
Cystic changes
Surgery
Radiotherapy
Chemotherapy
Paclitaxel
Chlorambucil
Doxorubicin
Vincristine
Etoposide
10
Fibrosarcoma:
Rhabdomyosarcoma:
A hypertrophic scar
Is treated by excision
A rich vasculature
11
Low mesenchymal density
Malignant melanoma
Freckles
Concerning melanoma
12
trunk and grows slowly
<1mm
1-1.5mm
1.5-2mm
2.1-4mm
>4mm
In non-whites
Genital sites
In stable diabetics
Rhabdomyosarcoma
13
Hepatic metastases occur very early
Rhabdomyosarcoma
Liposcraoma
Prognosis is poor
14
May present a jigger
Nodular
Fungating
Fleshy
Plaques
Visceral
15
In soft tissue sarcomas
Nodular
Subcutaneous
In subungual melanoma
16
The following are important in the assessment of melanoma
Tumour thickness
Presence of ulceration
Host response
Chest Xray
Serum LDH
Bowan’s Disease
17
Is 2-3 times more common in woman
Burno
Varicose vein
Pressure sore
Lonizing radiation
Chronic ulcers
Neurofibromatosis
Lymphangioma
18
hygroma
Answers
C
C, D
E
A, C
B, C, D
A
B, C
E
A, B
A, B, D, E
C, D
B, C, E
A
B, D
E
B, D
A, E
B, D, E
19
B
A, D
C, E
B, E
A, B, E
B, C,D
A, C
A, B, C, D, E
B, E
B
C, D, E
D, E
A, C, D, E
A, B
C, E
A, B, D
A, C, D
A, B, D, E
A, B, C, D
A, B, D
C, D, E
B
B, C, E
A, B, D
20
A, C, D
C, D, E
B, C, D
A, D, E
A, D, E
A, C, D, E
A, B, D
B, C, D
A, C, D, E
A, B, C, D
C, D, E
B, D, E
A. B, E
B, E
A, C, D
21
CHAPTER 44
ACUTE RENAL FAILURE, HAEMATURIA, HAEMATOSPERMIA
Acute renal failure:
Extra-renal failure:
1
Acute obstructive uropathy:
Entero-cutaneous fistula
Myocardial infarction
Radiation
Cortical necrosis
Pelvic neoplasia
2
Radiographic contrast media may cause renal damage
3
Acidosis in renal failure:
Pulmonary oedema
In peritoneal dialysis
Wound dehiscence
4
Polycystic kidneys
Recent laparotomy
In peritoneal dialysis:
Haemodialysis:
Disequilibrium syndrome:
5
Prevention is by slow but short periods of dialysis
The survival results after acute renal failure from tubular necrosis
is worse in:
Surgical patients
Non-surgical patients
ICU-patients
6
procedures
Haematuria:
due to:
Vesical schistosomiasis
Bladder calculi
7
Renal cell Carcimona
Prostatic calculi
Prostatitis
Schistosomiasis
Urethritis
VDRL is be indicated
Urethrocystoscopy is required
8
CHAPTER 44
ACUTE RENAL FAILURE, HAEMATURIA, HAEMATOSPERMIA
ANSWERS
9
A,C,D,E 25. A, B, C, D
A,B,C,D 26. A, B, C, D, E
A,B,C,D 27. A, B, C
A,B,D,E
A,B,C,D
A,B,C,E
A,B,D
B,D,E
C,E
A,B,C,D,E
C,D
A,B,C,D,E
A,B,C,D,E
A,B,D,E
A,B,E
A,B,E
A,B,C,E
C,E
A,C,E
A
10
A,C,E
B,C,D,E
A,B,C,E
B,E
11
CHAPTER 55
CANCER CHEMOTHERAPY
Hodgkin’s lymphoma
Thyroid carcinoma
Burkitt’s lymphoma
Choriocarcinoma
Malignant melanoma
1
Non-proliferating cells comprise:
Differentiated cells
Dying cells
Resting cells
Methotrexate
Thiotepa
5 Fluoro-uracil
Cytosin arabinoside
Adriamycin
Anti-metabolites:
2
Bind strongly and irreversibly to cellular enzymes thereby blocking
their activities
Nephroblastoma
Choriocarcinoma
Osteosarcoma
Gastric carcinoma
Methotrexate:
Haemorrhagic cystitis
Haemorrhagic enteritis
Stomatitis
Conjunctivitis
Myelo-suppression
3
Renal disease
Hypertension
Liver disease
Peptic ulcer
Diabetes mellitus
5-Fluoro-uracil:
Breast cancer
Ovarian cancer
Testicular carcinoma
Lung cancer
4
Liver damage
Gastro-enteritis
Nephrotoxicity
Alopecia
6-mercapto-purine:
Is a purine agonist
Is given intravenously
Is nephrotoxic
Alkylating agents:
DNA strands
5
Alkylating agents include:
Cyclophosphamide
Thioguanine
L-phenylalanine mustared
Bleomycin
Nitrogen mustard
Osteosarcoma
Bladder cancer
Breast cancer
Leukaemia
Haemorhagic cystitis
Alopecia
Diarrhoea
Exfoliative dermatitis
Nitrogen mustard:
Acts slowly
6
Is administered or intravenously
Vinblastine
Actinomycin D
Endoxan
Cisplatin
Daunorubicin
Actinomycin D:
7
Nephroblastoma
Malignant melanoma
Non-Hodgkin’s lymphoma
Choriocarcinoma
Atrophic dermatitis
Alopecia
Cardiomyopathy
Gastro-enteritis
Stomatitis
Osteosarcoma
Breast cancer
Childhood lymphoma
Astrocytoma
Cancer of thecervix
8
Transitional cell cancer of the bladder
Vincristine:
Is vinca alkaloid
treatment of:
Leukaemia
Lymphoma
Nephroblastoma
Rhabdomyosarcoma
Osteosarcoma
Peripheral neuropathy
Diarrhoea
9
Convulsion
Psychosis
Hepatic failure
control of:
Micrometastases
Nodal metastases
The combined drugs should act in the same phase of the cell cycle
to ensure maximum “kill”
10
Alkaline phosphatase
Serum calcium
Serum creatinine
Plasma proteins
cancer include:
Daunorubicin
Cyclophosphamide
5-Fluoro-uracil
Vinblastine
L-phenylalanine mustard
Dactinomycin
CCNU
Doxorubicin
Thiotepa
Cisplatin
Methotrexate
Mitomycin
Doxorubicin
11
Chlorambucil
Streptoxocin
Subcutaneously
Sublingually
Suppository
Topically
Orally
Surgery
Radiation
Immune modulation
Temperature modulation
Hydrotherapy
12
Body mass index of the patient
are necessary:
Haemoglobin level
Surface area
Visual acuity
13
The following measures are taken to prevent tumour lysis
syndrome:
Allopurinol
Lowering urinary pH
Blood transfusion
6-Mercaptopurine
5-Flurouracil
Actinomycin D
Cytosine Arabinoside
Cyclophosphamide
Halitosis
Loss of hair
Vomiting
Gall stone
Thrombocytopenia
14
Apoptosis
Dehydration
Neovascularization
Oxidation
Ion deprivation
CHAPTER 55 ANSWERS
A,C,D
A,D,E
B,E
B,C,D,E
A,C
A,C,D
B,C,E
15
A,B,D
B,C,E
A,C,D
A
A,D
B,C
B,D
B,C,D,E
A,C,E
B,D,E
A,B,D
A,D,D
B,E
A,B,D
A,E
A,D,E
A,B,C,D
B,C
A,C
A,B,C,D
A,C
B,C
A,C,E
A,B,D
16
B,C
A,C
AC
A,D,E
A,B,C,D
B,C
B,D
A,B,C,E
A,E
A, B,E
A,B,D
BCE
A
17
CHAPTER 56
ORGAN TRANSPLANTATION
Rejection:
Of hyperacute type can occur even when there are only minor
antigenic differences between the donor and the recipient
Upper limb
Bladder
Cornea
Skin
Pancreas
HL-A
DR Locus
1
ABO blood group
DR. Locus
HL-A
Rh factor
HLA
DR. Locus
Methotrexate
Prednisone
2
Cyclosporin A
Cyclosporin A:
Is a fungal peptide
Chronic pyelonephritis
Acute glomerulo-nephritis
Chronic glomerulo-nephritis
3
excluded as organ donors:
A. Hypothermia
B. Cerebral haemorrhage
C. Head injury
D. Drug overdosage
E. Cerebral thrombosis
11. Criteria for establishing brain-death include:
A. Absence of respiratory or spontaneous movement when the patient
is removed from the ventilator for one minute
B. Absence of response to deep pain
C. Absence of corneal reflex
D. Constricted fixed pupil
E. Absence of ocular deviation response when ice-cold water is run
into the
external auditory meatus
A. Subnormal temperature
B. Deteriorating renal function
C. Pain and tenderness in the region of the transplanted kidney
D. Leucopaenia
E. Swelling of the transplanted kidney
15. In acute rejection of a transplanted kidney:
4
The blood pressure falls
The weight of the patient falls and there may be slight oedema of
the ankle
Biopsy of the kidney shows massive infiltration of the parenchyma
by lymphocytes
Steroid dosage is increased
Further episodes are not likely to occur after the initial attack
16. The commonest cause of death after renal transplantation is:
A. Hypertension
B. Acute pancreatitis
C. Myocardial infarction
D. Secondary haemorrhage from the vascular anastomoses
E. Infection
17. The Complications of renal transplantation and its treatment
include:
Peptic ulceration
Tuberculosis
Neoplasm of the reticulo-endothelial system
Avascular necrosis of bone
Diabetes mellitus
5
It is not absolutely essential that the donor heart is re moved while
still beating
The donor heart must be plunged in ice-cold preservative fluid as
soon as it is removed and re-implantation may wait for 12h
An initial feature of rejection is an increase in the E.C.G. voltage
The average survival at 1 year is about 90% and at 5 years about
70%
21. Indications for liver transplantation include:
Liver metastases
Primary liver cell cancer without metastases
Cirrhosis of the liver without portal hypertension
Viral hepatitis with liver failure
Biliary atresia
22. Complications of liver transplantation include:
A. Cyclosporin A
B. Radiation
6
C. Prednisone
D. Azathioprine + corticosteroids
E. Monoclonal antibodies to T-cell
26. Tacrolimus:
7
30. Conditions that may lead to small bowel failure include:
A. Nercotising enterocolitis
B. Mesenteric infarction
C. Crohis disease
D. Exomphalos
E. Volvulus neonatorum
31. Complications of total parenteral nutritional (TPN) include:
A. Liver fibrosis
B. Recurrent severe dehydration
C. Recurrent shock
D. Sepsis (SIRS)
E. Multiple organ dysfuncion
8
CHAPTER 56
ORGAN TRANSPLANTATION
ANSWERS
A, B 26. B, D, E
C 27. C, D, E
D 28. D
B, C 29. B, C, E
B, C, D, E 30. A, B, C, E
B, D, E 31. A, B, D, E
A, C, D
E
B, C, E
A, D
B, C
A, B
A, D, E
B, C
C, D
E
A, B, C, D, E
A, B
A, B, C, D, E
A, E
B, E
A, C, D
A, B, E
A, B, C
E
9
CHAPTER 57
ANAESTHESIA
Drugs used in the pre-anaesthetic period for their effect on the central
nervous system include:
Pethidine
Hyoscine
Phenoxybenzamine
Diazepam
Propranolol
Papaveratum (Omnopon):
Inhibits vomiting
Depresses respiration
Causes sedation
Pethidine:
Pentazocine (Sosegon):
1
Is derived from nalorphine, a morphine agonist
Tranquillizers:
Reduce excitement
Induce sleep
Produce calmness
Produce analgesia
Phenothiazines:
Neuroleptics include:
Methadone(physeptone)
Promethazine
2
Haloperidol(serenase)
Chlorpromazine
Nitrazepam(mogadon)
Butyrophones:
Diazepam:
Is a phenothiazine
Hyoscine:
3
Phenoxybenzamine
Propranolol
Alprenolol
Atropine
Lorazepam
Propranolol
Pethidine
Oxprenolol
Morphine
Chlorpromazine
Tachycardia
Severe bradycardia
Cardiac arrest
Arrhythmia
Infarction
4
Stimulate respiration because of acidosis
Penicillin
Streptomycin
Kanamycin
Chloramphenicol
Neomycin
In chronic alcoholics :
5
Large doses of anaesthetic agents are required
The partial pressure of the agent in the alveolar air, blood and tissues
The more soluble the agent, the quicker its cerebral uptake
6
Nitrous oxide and cyclopropane are relatively insoluble in blood
Thyrotoxic patient
Aged
Shocked patient
Frightened patient
Dehydrated patient
Struggling
Breath-holding
Dilated pupils
Vomiting
7
arrest:
Enflurane
Ether
Halothane
Nitrous oxide
Isoflurane
Nitrous oxide
Choloroform
Cyclopropane
Ether
Ethyl chloride
Nitrous oxide:
Etomidate
8
Soluble in intralipid, ethyl glycol and ethanol
Midazolam:
It is a recommended anticonvulsant
Halohane
Diethyl ether
Cyclopropane
Nitrous oxide
Methoxyfluorane
Halothane:
Gives rapid and smooth induction and delayed recovery with short
9
anaesthesia
Metronidazole
Sex
Age
Desflurane
Nitrous oxide
Enflurane
Halothane
Diethylether
10
Anaesthetic agents that cause a fall in the blood pressure include:
Nitrous oxide
Halothane
Ether
Sevoflurane
Isoflurane
Thiopentone
Propofol
Etomidate
Ketamine
Methohexitone
Thiopentone:
Thiopentone:
Total dose at any one time should not exceed 500mg to prevent liver
dysfunction
11
Patients can handle machinery or drive 6h after recovery from it.
Thiopentone:
Is a satisfactory and safe anaesthetic as the sole agent for short procedures
such as diagnostic D & C
Causes severe spasm of the injured vessel with disappearance of the radial
pulse
Neostigmine:
12
Is available as the bromide or the methylsulphate
Ketamine:
Maintains pharyngeal and laryngeal muscle tone and reflexes and so the
airway
Ketamine:
Can be used to induce poor risk patients and for short procedures
13
Thiopentone
Propofol
Eomidate
Methohexitone
Ketamine
Muscle relaxants:
Acetyl choline is formed from acetic acid and choline in the presence of
coenzyme A and stored in vesicles at the nerve terminals.
Non-depolarizers include:
Vecuronium
14
Suxamethonium
Cisatracurium
Pancuronium
Decamethonium
Desensitizing block:
Suxamethonium:
Causes muscle paralysis of more rapid onset and shorter duration than
suxemethonium
Tubocurarine:
15
Crosses the placental barrier but not in sigficant amounts to have any
action on the foetus
Does not cause hypotension because its ganglion blocking effect is very
weak
Neostigmine:
Is a synthetic anticholinesterase
16
Causes tachycardia, salivation and stimulation of the bladder and gut
Nitrous oxide
Air
Oxygen
Carbon dioxide
Ethylene oxide
K Pa-8.98
K. Pa-98
K Pa-5.98
K Pa-2.33
K Pa-1.33
The best aid against fitting a cylinder to the wrong outlet of the
anaesthetic machine is:
17
With large bore tube and expiratory valve forms Macintosh circuit
21%
25%
30%
35%
40%
Has no valves
18
To prevent retention of carbon dioxide fresh gas flow of at least twice the
patient’s minute volume is required.
For a fit adult breathing spontaneously the gas flow per minute should
be at least:
Cooking
Taking an analgesic
A patient who has had general anaesthesia in the outpatient should not
be discharged if:
19
He is an asthmatic
He has no escort
Pain
Touch
Temperature
Propioception
Pressure
Alpha fibres
Beta fibres
Delta fibres
B fibres
C fibres
Prevents arrhythmia
20
Vasoconstriction
Myocardial depression
Intravenous fluids
Injection of atropine
Injection of morphine
Administration of oxygen
Convulsions, restlessness
21
Crying and hyperventilation
Slurred speech
Coma
Hemiplegia
Thiopentone
Diazepam
Oxygen
Artificial ventilation
Cortisol
Methaemoglobinaemia:
Cocaine
Is used as a surface analgesic for corneal analgesia and as a spray for the
nose, throat and larynx
22
Has a maximum dose of 100mg in an adult
Is a potent vasodilator
Procaine:
Is decomposed by boiling
In 1-2% solution acts within 2-5 minutes of infiltration and is effective for
1h
Is more toxic than lignocaine and toxic symptoms include convulsions and
dyspnoea
Mepivacaine
Lignocaine:
Is used for local infiltration, peripheral nerve block and epidural block
23
Recommended concentration for local infiltration is 2-4% and for
peripheral nerve block 1-2% and the maximum safe dose without
adrenaline is 400mg
Bupivacaine:
Nitrous oxide
The axillary approach is through a point 1 cm below and 3cm lateral to the
mid clavicle, the needle being directed posteriorly for 2cm
24
The supraclavicular and not the axillary approach may cause paralysis of
the phrenic nerve
At the end of operation the blood pressure cuff is removed all at once.
Tachycardia
Excitement
Convulsion
Giddiness
In Spinal analgesia:
25
The lumbar puncture can be performed between L1 and S2
A line connecting the highest points of the iliac crests passes through L3
or inter-space L3-L4
The spread of the block depends on the site of injection and volume of
agent injected
The spread of the block is not affected by the rate of injection of the agent
In spinal analgesia:
Testing analgesia by pinching the skin with artery forceps causes less
discomfort to the skin
Patient then lies supine or on the same lateral side of the planned
procedure
26
Characteristically sets in within 24-72h after the spinal
Gets worse in the sitting or upright position and diminishes in the lying
position
May be prevented by nursing the patient in the first 12h on a bed with the
foot end slightly raised and advising the patient not to read or smoke
during this period
Resting in the patient on a bed with the foot end raised relieves it
Ascending myelitis
Meningo-encephalitis
27
Reduced incidence of post-operative bleeding
Headache is rare
1% : 20ml (200mg)
1% : 15ml (150mg)
28
2% : 10ml (200mg)
Because of its long duration of action esmolol is used for the resection of
pheochromocytoma
Propofol:
Is an aqueous emulsion
The expiratory valve which is near the anaesthetic end of the circuit must
be fully open during use.
29
For laryngoscopy
The landmark for the intubation is the epiglottis which is posterior to the
larynx
Methohexitone
Thiopentone
Ketamine
Etomidate
Propofol
In conscious sedation
30
vertebrae to fuse
CHAPTER 57
A, D
31
C, E
D
B
B,D
A, B, D
B, C, D
A, C, D
A. C
B, C
B, C
A, C,D
B, D
C
A, B
B, C, E
A, C
C, D, E
A, B, D, E
B, C, D
B. C. E
A, B, E
A, B, C
A, B, D, E
B, C
32
A, C, E
A, C, D
A, D
B, C
B
E
B, E
D
B, D, E
D
C, D
A, E
C
A, C
C
A
A, B, C, D
A
A, E
C, D
A, C, D
A, C
A, D
B, C, D
33
E
B, D
A, B, E
B, C
B
D
B, D
B, D
C
A, C, D, E
B,
A, B, D
A, B, D, E
A, C
E
A, B, E
A
B, D
B, C, E
A, B, C, D
A, B, C, D
A, C
B, D
A, C, E
34
A, B, D
A, B, C, D
A, B, C, E
A, B, C, D
A, D
C, D
A, C, D
C
D
B, C, D
A, B, D
A, C
B, C, D, E
A, B, D,E
A, C
A, C, D, E
A
B, C
A, B, C, D, E
D
C
A, B, C, E
A
C
35
36
CHAPTER 58
PRINCIPLES OF RADIOTHERAPY
Ionising radiation:
May raise the energy level of an electron within the atom making
the atom more reactive – excitation
1
the radiation
If high implies that the radiation dissipates its energy within a very
short distance, no more than the thickness of a tissue paper
DNA
Genes
Cytoplasm
Cell membrane
2
Is high if the partial pressure at the time of irradiation is low
Its site
1000cGy weekly
The biological effect does not generally decrease as the dose rate
decreases
3
100cGy to the whole body will cause aplastic anaemia
Patient is young
4
Pigmentation
Thickening
Dryness
Epilation
Transient erythema
Oedema
Depigmentation
Dry desquamation
Excoriation/moist desquamation
Loss of taste
Dysphagia
Dental atrophy
5
Frequency of micturition
Haematuria
Dysuria
Retention of urine
Strictures
Granulomata formation
Malabsorption
Perforation
dose of (cGy):
500
1000
1800
3000
4000
Headache
6
Anorexia
Diarrhoea
Malaise
weight loss
Epistaxis
7
All living things are exposed to background radiation from:
Granites
Sea
Soil
Sun
Air
Australian whites
Albinos
Depigmentation
Hyperkeratosis
Cracks
Fissures
Ulcers
Skin cancer
8
Dermatitis
Leukaemia
Osteosarcoma
Malformations
Pre-operative radiotherapy:
A. Malignant melanoma
C. Kaposi’s sarcoma
E. Mycosis Fungiodes
9
surgery
Papillary carcinoma
Medullary carcinoma
Anaplastic carcinoma
Follicular carcinoma
Lymphoma
Local recurrence
Inoperable tumour
Bone metastases
Gastric carcinoma
Gastric lymphoma
10
Squamous carcinoma of the anus
11
CHAPTER 58
PRINCIPLES OF RADIOTHERAPY
ANSWERS
A, D
C, D
A, B, C
A, B, C, D, E
A, B, C, E
B
A, B
A, B, C, D
D
C,
12
A, B, C, D, E
A, B
B, C, D
A, D, E
B, D, E
A, C, D
A, C, D, E
C
A, B, C, D, E
C, D, E
A
C, D
B, C, D
B, C, D
A, B, C, D, E
A, C, E
C
A, B
A, D
A, B, C, E
A, B, E
A, D,E
C, D,E
13
14
CHAPTER 60
1
The baby should be nursed on the lateral side
Feeding is done with the baby lying prone over the mother who is in
the supine position
Tube feeding is occasionally necessary
The crisis is usually over by 3 months after birth
2
Biliary atresia
Persistent copious bile-stained vomiting within 48h of birth may
be
due to:
Accurate history
Promptness of differential diagnosis and examination
The quality of nursing care
The ambience of the theatre setting
The competence of the surgeon
The following congenital malformations can be treated
conservatively:
Micrognathia
3
Pneumothorax
Thymoma
Tracheal collapse
Naevus of the zygomatic areas
Developmental abnormalities:
Developmental abnormalities:
4
CHAPTER 60
A, C, D
B, D, E
B, C
B, C
C, D, E
A. C, E
B, C
B, D
B, E
C
A
A, B, E
B, C
D, E
5
C, E
A, B
C, E
6
CHAPTER 61
ULTRASOUND SCANNING COMPUTERIZED TOMOGRAPHY
MAGNETIC RESONANCE IMAGING AND RADIOISOTOPE
SCANNING
The following statements are true about ultrasound imaging:
1
Cysts usually are associated with back-wall enhancement.
Which of the following are not indications for duplex and colour
doppler sonography:
The greater the density of the matter in the path of the x-ray beam,
the darker the image.
2
It utilizes ionizing radiation
Bone has low proton density and hence gives off high signal
intensity.
3
Xenon or krypton gas may be used for perfusion studies.
4
CHAPTER
IMAGING
B, D
A, B, D, E
5
B, C, D, E
A, D
C, D, E
A, C, E
B, D
A, C, E
B, C
A, B, E
6
CHAPTER 62
DAY SURGERY
1
varicose veins, abscesses
Severity of pathology
Duration of disease
Patient’s living distance from hospital
Demonstrable willingness to abide by care instructions
2
The wounds should be closed with absorbable subcuticular
suture if possible
The wound should be covered with transparent dressing
There should be no interference with the dressing until the
wound is healed
The wound needs to be inspected before discharge from centre
to ensure all bleeding has ceased
The state of the wound is recorded before discharge
3
B. Increased use of hospital personnel
C. Increased availability of financial resources
D. Increased visitation of doctors
E. More efficient use of time
11. Contra-indications to day care surgery in children include:
A. Long distance from the home
B. Preterm delivery of a child
C. Lack of education of parent
D. Absence of community health nurses
E. Low socio-economic status of parent
12. Co-morbid conditions that may make day care surgery unsafe
include:
A. Sickle cell disease
B. Cardiac failure
C. Extra-digit
D. Pre-auricular skin tag
E. Renal anomaly
13. Indications for day care surgery in children include:
A. Inguinal hernias
B. Hydrocoles
C. Umbilical hernias
D. Rectal Biopsies
E. Circumcisions
4
14. Those who must be involved in preparing a child for day care
surgery
include:
The parents mainly
The surgeon mainly
The Anaesthetist mainly
The nurse mainly
All of the above
15. It is not possible to do day care surgery without the following:
A. A community health nurse
B. Internet facilities
C. Good Communication system
D. Good transportation system
E. A ward dedicated solely to day care surgery
CHAPTER 62
DAY SURGERY
ANSWERS
A
A, B, C, D, E
A
A, B, C, D, E
B
A, B, C, D, E
A, B, C, D, E
A, B, E
5
A, C
A, E
A, B
A, B, E
A, B, C, D, E
A, B, C, D, E
C
6
CHAPTER 63
MINIMALLY INVASIVE SURGERY
The following lesions can be diagnosed using the colonoscope:
Intussusception
Polyps
Ulcerative Colitis
Diverticular disease
Volvulus
Metabolic acidosis may occur with the most commonly used gas
Hand-eye co-ordination
2D vision
Complications of pneumoperitoneum
1
In laparoscopic surgery:
The two methods for gaining access are with the Verres needles
and the Hasson technique
Cardiac arrhythmias
Air embolism
Diffusion hypoxia
2
Confirmation of duodenal perforation
Laser ablation
Band ligation
Video camera
Light source
Verres needle
Turbulence of gas
Mechanical inoculation
Tissue trauma
3
Complicaions include formation of bullae
CHAPTER 63
MINIMALLY INVASIVE SURGERY
ANSWERS
A, B, C, D, E
C, D, E
A, B, C, E
A, B
A, C, E
A, C, D
B, C, D, E
B, C, D
A, B, C
A, E
4
5
CHAPTER 22
THE THYROID AND PARATHYROID GLAND
A. Isthmus lies in front of the first, second and third tracheal rings
B. Weight of the gland is 7-25 g in the African
C. “Strap muscles” consist of the sternothyroid, sterno-hyoid and the
inferior belly of the omo-hyoid
D. Medial relations of the lateral lobes are the hyoid, thyroid and cricoid
cartilages
upper six tracheal rings, oesophagus and recurrent laryngeal nerve
E. Superior and middle thyroid veins drain into the internal jugular vein
and the
Inferior thyroid veins into the innominate vein
Serum T3 concentration
T3 resin uptake
Serum T4
Serum free thyroxine
Free T4 index
Free T4 index
Serum thyroid stimulating hormone
Test of hypothalamic-pituitary axis
1
Protein bound iodine
Serum T3 concentration
5. In thyroid scan:
6. Thyroglossal cyst:
7. Goitre:
Exists when more than 10 per cent of any community have goitre
Does not occur in West Africa
2
Is caused principally by low iodine content of the local soil
Is caused by cassava containing cyanogenic glucosides in some parts
of Africa
Affects adolescent boys and girls in roughly the same ratio
Hoarseness of voice
Snoring during sleep
Difficulty in swallowing
Oedema of face and conjunctivae
Engorged manubrial subcutaneous veins
May occur at any age from the neonate to the elderly but the peak
incidence is from 21 to 30
Affects women five times more than men
Is symptomless in the vast majority of patients(apart from the
swelling)
Is multinodular involving both lobes in about 50 per cent of patients
Feels soft or firm and has indefinite edges
3
A. Is seen more commonly in endemic areas
B. May affect children
C. Is seen most commonly in girls from around puberty to 20
D. Is a uniformly enlarged and soft thyroid gland
E. Does not become big enough to compress the trachea
Tetany
Infection
Sudden haemorrhage
Malignancy
Myxoedema
X-ray of neck
Free thyroxine index
Serum T3 concentration
Direct laryngoscopy
Isotope uptake test
A. Administration of thyroxine
B. Excision
C. Lobectomy of the affected lobe
D. Administration of Lugol’s iodine
E. Subtotal thyroidectomy
Administration of thyroxine
Subtotal thyroidectomy
Administration of Lugol’s iodine
Lobectomy
Radio-iodine
19. Thyrotoxicosis:
4
If primary, is associated with a pre-existing diffuse hyperplastic
goiter
If secondary, may be associated with malignant thyroid
May be precipitated by ingestion of large doses of iodine in a patient
with long-standing goitre
Is uncommon in Africans
20. In thyrotoxicosis:
22. The following is/are found in the orbit and extraocular muscles in
exophthalmos
Erythrocytes
Plasma cells
Giant cells
Polymorphs
Reticulocytes
Constipation
Insomnia
5
Gynaecomastia
Oligomenorrhoea
Tiredness
Moist hands
Auricular fibrillation
Lid lag
Palpable thyroid
Hyperkinetic movements
26. Exophthalmos:
Conjunctival oedema
Diplopia
Corneal ulceration
Diminishing visual acuity
Directly related to the severity of hyperthyroidism
6
29. The thyroid gland in thyrotoxicosis:
Weight loss
Blood pressure
Sleeping pulse rate
Restlessness
Appetite
Primary thyrotoxicosis
Meningioma
Carotid-cavernous fistula
Optic nerve glioma
Orbital tumour
7
to tyrosine
Potassium perchlorate prevents trapping of iodine and coupling of
MIT and DIT to T2 and T4
Carbimazole prevents binding of iodine to tyrosine and coupling of
MIT and DIT to T2 and T4
Phenobarbitone relieves palpitation and excessive sweating
Diarrhoea
Arthralgia
Skin rashes
Depression
Anaemia
8
38. Radio-active iodine:
Depresses the activity of most of the thyroid cells but does not
destroy them
Is fully effective in 4 weeks
May induce carcinomaof thethyroid in the elderly
Is only given to patients over 55 years
Leads to hypothyroidism in 40-50% of the patients in 5 years
41. Propranolol:
Is an alpha-blocking agent
Controls the symptoms and signs of thyrotoxicosis because it can
depress the production of thyroxine
Is effective within 24 h of administration and the dose is80 mg orally
daily
Is usually given for 4-7 days before and 10-14 days after subtotal
thyroidectomy
Is currently preferred to the usual anti-thyroid drugs for making toxic
patients euthyroid
42. Soon after the removal of the endotracheal tube after subtotal
9
thyroidectomy
for secondary thyrotoxicosis, a patient is found to be having
severe difficulty
in breathing.
Is permanent
If unilateral causes hoarseness of voice and non-productive cough
If bilateral causes severe hoarseness of voice and difficulty in
breathing
If bilateral requires early repair of the nerves
If bilateral and there is no recovery after one year, requires
arytenoidectomy with lateral fixation of one cord
10
46. Hypoparathyroidism after subtotal thyroidectomy:
Is fairly common
Is caused by excessive release of TSH in the post-operative period
Is characterized by excitation, profuse sweating, hyperpyrexia and
and tachycardia
Is treated with propranolol, Lugol’s iodine, carbimazole, diazepam and
intravenous fluids
May require oxygen administration and cold sponging
11
Abortion
Postmature labour
Stillbirth
Eclampsia
Foetal goitre and hypothyroidism
54. Hypothyroidism:
12
or aspirin
If congenital is always associated with a goitre
In the adult is not associated with a goitre
If congenital causes mental and physical underdevelopment
sometimes
with deaf-mutism
13
A. Pain or discomfort in the thyroid area of the neck
B. Severe hyperthyroidism
C. Hypothyroidism
D. Nodular goitre
E. Solitary nodule
Is fairly common
Is seen from childhood to old age with a peak incidence in Africa
In the 4th decade
Is 3 times more common in men
May arise in a nodular goitre
May present with hypothyroidism
14
predominantly
mixed papillary and follicular carcinoma
E. Heredity is a factor in some cases of medullary carcinoma
15
67. A 35-year old woman presents with a solitary thyroid nodule which
has been
present for about 4-years, but has recently been enlarging. It is firm,
rather
circumscribed and fairly mobile. There are no enlarged cervical
lymph nodes.
A. A cyst
B. An adenoma
C. Nodular goitre
D. Papillary or follicular adenocarcinoma
E. Anaplastic carcinoma
68. If the scan shows it to be “hot” with some uptake in the rest of the
thyroid,
you will consider:
A. A cyst
B. An adenoma
C A papillary or follicular adenocarcinoma
D. Nodular goitre
E. An autonomous nodule
69. If the scan shows it to be “cold”, you will consider:
A cyst
An adenoma
A papillary or follicular carcinoma
Nodular goitre
An autonomous nodule
Horner’s syndrome
Cervical lymphadenopathy without thyroid swelling
A pulsatile skull swelling
Hyperthyroidism
Diarrhoea
16
71. Measures taken in the treatment of operable papillary or follicular
carcinoma
of the thyroid include:
Near-total thyroidectomy
Irradiation
Radio-active iodine
Cytotoxic therapy with adriamycin or bleomycin
Administration of thyroxine
Near-total thyroidectomy
Irradiation
Radio-iodine
Cytotoxic therapy with bleomycin and adriamycin
Administration of thyroxine
84% and 60% of those with papillary carcinoma are alive at 5 and 30
years
60% and 40% of those with follicular carcinoma are alive at 5 and 30
years
No patient with anaplastic carcinoma is alive at 3 years
Those over 40 have a better prognosis than those under 40
Women have a better prognosis than men
Palpitations
Profuse sweating
Progressive weight loss inspire of polyphagia
Consistent heat intolerance
Diarrhoea
17
Moist hands
Atrial fibrillation
A sleeping Pulse Rate > 120/min
A sleeping Pulse Rate > 90/min
Pretibital mxyoedema
18
Benign solitary nodule
Hashinoto’s thyroiditis
Lymphadenoid goitre
Papillary carcinoma of the thyroid
Medullary carcinoma of the thyroid
19
Convulsions
Stridor and dyspnoea
Excessive sweating
Pyrexia
Restlessness
85. Late complications of hypoparathyroidism include:
88. Hyperparathyroidism:
Is an uncommon disease
Is more common in men
May be seen at any age
May be symptomless
May precipitate acute pancreatitis
20
Anorexia
Nausea and vomiting
Muscle cramps
Numbness around the lips, polyuria and polydipsia
Restlessness
Sclerotic skull
Subperiosteal resorption of bone seen particularly in the
middle phalanges of the index and middle fingers, upper part
of the tibia and neck of the femur
Nephrocalcinosis
Periosteal thickening of the radius and ulna
Calcification of the spleen
92. In hyperparathyroidism:
21
Excessive intake of antacids
Multiple myelomatosis
Sarcoidosis
Osteitis deformans
Multiple bone metastases
Severe weakness
Abdominal cramps
Copious vomiting
Irritability
Drowsiness
22
CHAPTER 22
THE THYROID AND PARATHYROID GLAND
ANSWERS
A, B, E
A, B, D
D
B
C
D, E
D, E
B, C, D, E
A, C, D, E
B, D, E
A, B, C, D, E
A, B, C, D, E
C
A, B, C, D
C, D
23
A
C
A, B, C
C, D
B, E
B, D, E
B
B, C, D, E
A, C
A, B, D, E
A, D
A, B, C, D
B, C, D
B
B, D
C, E
A, B, C, D, E
D
A, C, D
A
24
B, C, E
C
E
A, E
A, C, D
C
D
C, D, E
A
B, E
B, E
C, E
A
A, B, D
A, C
A, D
A, C
C, D
B, E
A, C, D
25
A, C
A, D
A, C, D
B, D
B, C
B, D
A, E
A, B, D
A, D, E
A, C, E
A
B
B, E
A, B, C, D
A, B, D, E
A, C
B, D
A, B, E
D
D
26
B, E
A
B
E
C
D
C, D, E
A, D, E
A, B
B, C, E
C, D
C, E
A, C, D, E
A, B, D, E
E
B, C
A, C, D
B, C, E
A, C, D, E
C, D, E
27
B
28
SURGERY
CHAPTER 23
THE NECK
A. Epiglotis
B. Common carotid artery
C. External jugular vein
D. Internal jugular vein
E. Brachial plexus
A. Horner’s syndrome
Aerial fistula
C. Dysphonia
1
D. Mediastinitis
E. Surgical emphysema
Ludwig’s angina:
A branchial cyst:
A branchial fistula:
2
pit
C. Usually presents around puberty
D. Opens at the junction of the middle and lower thirds of the anterior
border of
the sternomastoid
A cystic hygroma:
Occurs in the posterior triangle of the lower third of the neck, axilla
or cheek
Chemodectoma:
A. Lymph node
B. Lipoma
C. Sternomastoid tumour
D. Aberrant thyroid
3
E. Neurofibroma
A. Thyroglossal cyst
B. Dermoid cyst
C. Brancial cyst
D. Sebaceous cyst
E. Ranula
A 25 year old man has a 3 month old, painless swelling below the
angle of the mandible. It is tense, fluctuant mobile, and most
deep to the sternomastoid
A. Chronic abscess
B. Pharyngeal diverticulum
C. Lipoma
D. Branchial cyst
E. Laryngocele
A. Metastases
B. Hodgkin’s lymphoma
C. Tuberculosis
D. Sarcoidosis
4
E. Multiple neurofibromatosis
A. Larynx
B. Right lung
C. Stomach
D. Pancreas
E. Right breast
A. Chemodectoma
B. Lymph node
C. Parotid tumour
D. Submandibular salivary gland tumour
E. Lipoma
In Ludwig’s angina:
5
C. Excessive salivation and trismus are presenting symptoms
D. Broad spectrum antibiotics such as cefuroxime and metronidazole
should be
Administered
E. The tongue is oedematous and is displaced upwards and forwards
6
B. The ESR may be normal
C. Screening for HIV is not essential
D. The Mantoux test, unlike in pulmonary tuberculosis, is usually
unremarkable
E. Excision biopsy may be necessary to establish the diagnosis
Branchial cyst:
Brancial fistula:
A. Arises from failure of the second branchial arch to fuse with the fifth
arch
B. Arises from failure of the first branchial arch to fuse with the fourth
arch
C. Has abundant lymphoid tissue in the wall
D. Should be excised through 2 or 3 small transverse incisions over the
course
of the tract
E. Is lined by columnar and ciliated epithelium in its inner portion and
stratified
squamous in its outer portion
Cystic hygroma:
7
C. Is best treated by sclerotherapy as this has been found to be very
effective
D. Is completely compressible
E. Has a 90% chance of recurrence following excision
8
9
CHAPTER 23
THE NECK
ANSWERS
A, C, D
E
B, C, D, E
C, E
A, E
C, D, E
B, C, E
A, D
C
B
D
A
A, B, C
B, C
A
A, B, C, D
C, D, E
10
A, E
A, B, C
A, C, D, E
A, B
B, C
11
CHAPTER 25
DIAPHRAGM
1
Level of T10 and 2.5 cm to the left of the mid-line
diaphragm?
Occurs at T10 level and 1cm away from the site of entry for the
right phrenic nerve
2
Occurs at T11 level and transmits the right phrenic nerve
3
C. The central tendon is level with junction of the 6th costal cartilage
with the
sternum
D. The largest foramen is at level of the 12th dorsal vertebra
E. The oesophageal opening is at level of 10th dorsal vertebra
F. The oesophageal opening also transmits the two vagi and the
branches
of the left gastric artery
G. The inferior vena caval opening is at level of the 8th dorsal vertebra
H. The caval opening also transmits the right phrenic nerve
Hookworm infestation
Chronic cholecystitis
Reflux oesophagitis
4
Oesophageal and gastric motility studies
Oesophago-gastroduodenoscopy
Oral cholecystogram
Oesophageal stenosis
Haemorrhage
Water brash
Nocturnal dyspepsia
5
The most essential element in repair of hatus hernia is:
oesophagus
6
At the lower oesophageal sphincter (LOS):
A critical pressure of < 6mmHg and sphincter length of < 1cm carry
a 90% chance of reflux
A critical pressure of < 12mmHg and sphincter length of < 2cm
carry
a 90% chance of reflux
A critical pressure of < 18mmHg and sphincter length of < 3cm
carry
a 90% chance of reflux
A critical pressure of < 24mmHg and sphincter length of < 4cm
carry
a 90% chance of reflux
A critical pressure of < 30mmHg and sphincter length of < 5cm
carry
a 90% chance of reflux
7
month.
B. Gallstone colic
C. Subacute pancreatitis
Myocardial infarction
Subacute appendicitis
Oesophageal carcinoma
8
hiatal
hernia include:
The three criteria that must obtain to warrant surgical anti reflux
procedure are:
9
oesophageal
contractility
In para-oesophageal hernia:
10
The mixed hiatal hernia:
hiatal nernia
11
31. A woman of 60 presents with epigastric pains radiating to the
retrosternal
Ultrasonography
12
33. The procedure of choice in the management of this patient is:
35. The most frequently used anti reflux procedure currently is:
13
C. The Hill gastropexy – fundus to accurate ligament
E. Sliding hiatal
14
abdomen
hemithorax on X-rays.
Spontaneous pneumothorax
15
40. A child of four presents with shortness of breath on exertion,
dyspnoea
soon after exertion and the left side of the chest is tympanitic.
Plain
16
E. Thoraco-abdominal exploration
43. A neonate presents two hours after birth with acute respiratory
distress, tachypnoea, grunting and cyanosis. On examination
there is a mediastinal shift to the right with typanitic note on
percussion on the left. The abdomen is unremarkable.
17
D. Ultrasonic study of the chest
E. Xenon radio scan of the chest and abdomen
18
A. Plain x-ray of chest P.A and Lateral
D. Abdominal ultrasound
19
A. Pericardial tumour
B. Sliding hiatal hernia
C. Tumour of the diaphragm
D. A left parasternal hernia (Morgagni hernia)
E. Chronic pancreatitis
B. Chronic cholecystitis
20
51. The most useful diagnostic investigation is:
C. Gastric ulcer
D. Duodenal ulcer
A. Meningitis
B. Encephalitis
21
C. Cerebral haemorrhage
D. Cerebral tumour
E. Pleurisy
A. Pericarditis
B. Aortic aneurysm
C. Subphrenic abscess
D. Haemoperitoneum
E. Mediastinal tumours
singultus (hiccups)?
22
Rebreathing in a paper bag
C. Has two domes which rise in full expiration as high as the 4th
23
59. Hiatus herniae:
diaphragm only
developing countries
E. Are usually of the sliding type (85%) and rarely of the para-
24
E. If asymptomatic requires no treatment
apparently foreshortened
Complications
25
62. Sliding hiatus hernia:
by pH studies
oesophagus
again incompetent
and incompetent
26
B. The fundal bulge is usually into the left pleural cavity
in the mediastinum
27
D. Should endeavour to restore the acute angle between oesophagus
and stomach
stabilized infant
A. Occurs through the potential defect between the costal and sternal
fibres
of the diaphragm
28
A. Results from partial or complete failure of the embryonal cervical
diaphragmatic hernia
D. Is usually asymptomatic
29
30
CHAPTER 25
DIAPHRAGM
ANSWERS
1. C 38. A
2. A 39. C
3. A 40. A
4. B 41. C
5. B 42. C
6. D 43. D
7. D 44. B
8. B 45. D
9. A, B, C, D, E, F, G, H 46. A
10. D 47. C
11. D 48. D
12. A, B, C 49. D
13. D 50. E
14. A, B, C 51. E
15. B 52. D
16. A 53. A, B, E
17. A 54. A, B, C, D, E
18. D 55. A, B, C, D, E
19. A 56. A, B, C, D
20. B, C 57. A, B, C, D, E
21. D 58. A, B, C, D, E
22. C 59. A, B, C, D, E
23. C 60. A, B, C, D, E
24. A, B, C, D, E 61. A, B, C, D
31
25. A, B, C, D, 62. A, B, C, D, E
26. A 63. A, B, C, D, E
27. A 64. B, C, E
28. A 65. A, B, C, D
29. A 66. A, B, C, D, E
30. B 67. A, B, D, D, E
31. D 68. A, B, C, D, E
32. A 69. A, B, C, D, E
33. E
34. A, B, C, D, E, F
35. B
36. A
37. C
32
CHAPTER 28
THE BREAST
The average normal breast overlies the:
2nd – 7th ribs
Pertoralis major
Serratus anterior
Upper part of rectus sheath
Intercostal muscles
In the anatomy of the breast
The structural unit is the lobule
There are 20-25 lobes each formed by the coalescence of groups of
lobules
Lactiferous ducts, each draining a lobe, open separately and
radially on the summit of the nipple
The bulk of the areola and nipple is made up of contractile smooth
muscle fibres inserted directly to the skin
The skin of the nipple and areola is thin, sensitive and contains
large sebaceous glands and hair follicles
In the lymphatic drainage of the breast:
The internal mammary chain of lymph nodes drains about 20% of
lymph mainly from the medial aspect
The axillary group of lymph nodes drains about 50% of lymph
mainly from the lateral side
Some lymph drains to the opposite breast and axilla and the liver
Malignant cells necessarily metastasize to lymph nodes draining
the corresponding breast quadrant
Retrograde tumour emboli are the rule when a forward system of
lymphatics is blocked.
Increase in the size and number of the mammary lobules occurs
in:
Puberty
Menstruation
Pregnancy
Lactation
Normal growth
The normal breast depends on the following for its full
development and growth:
Cortisone
Prolactin
Oxytocin
1
Oestrogens and progesterone
Growth hormone
2
Adrenal tumour
Constitution or genetic predisposition
3
Reassurance if the whole or both breast are affected
Excision biopsy for definite localized mass
Danol orally for 2 months
Simple mastectomy in those over 40years
Aspiration of cysts
Duct ectasia:
Is dilatation of the lactiferous ducts
Occurs between 25 and 70 but especially between 25 and 35
Is seen equally in all parts of the breast
Results from obliteration from fibrosis and ageing of the periacinar
and perilobular lymphatics
Leads to the accumulation of yellow or brown cheesy material in the
ducts which can be expressed like toothpaste
Structures seen in the microscopic picture of duct ectasia
include:
Plasma cells
Lymphocytes
Fibrous tissue
Lipid material
Giant cells
Duct ectasia may present as:
Retraction of the nipple
Turbid yellow, green, brown or black nipple discharge
Mammillary fistula
Areolar swelling with attachment of skin, surrounding tissue and
axillary
lymphadenopathy
Subareolar abscess
Measures taken in the management of duct ectasia include:
Reassurance
Observation
Excision biopsy
Simple mastectomy
Oestrogen and antibiotic therapy
In traumatic fat necrosis:
The patients are obese
There is in most patients a history of trauma to the breast
Saponification of fat by blood and tissue lipase causes a foreign
body inflammation
4
There is fibrous tissue with spaces containing liquefied fat, fatty acid
crystals and chalk-like material in the centre
Irritation of cells may precipitate cancer formation
A lump in traumatic fat necrosis:
Is soft to firm
May be attached to skin and has irregular surface
Has indefinite edges
Is usually attached to the underlying muscle
May cause retraction of the nipple
A breast cyst:
May contain a papillary carcinoma in its wall
May be caused by benign mammary dysplasia or traumatic fat
necrosis
May occasionally be caused by intraduct carcinoma
Occurs in the lower outer quadrant in most patients
Is best excised
A cyst of the breast should be excised if after aspiration:
The lump does not disappear completely
The fluid obtained is greenish or brown
The lump reappears within 2-4 weeks
There is pain in the breast
Other cysts appear
Measures that may be taken in the management of galactocele
include:
Cold compress
Massaging of the lump
Aspiration
Stopping feeding on the affected breast
Excision biopsy initially to exclude malignancy
The clinical signs of a chronic breast abscess include:
Hard consistency
Tenderness
Indefinite edge
Peau d’orange
Enlarged axillary lymph nodes
Pericanalicular fibroadenoma
Occurs in the age group 14-45 with a peak around 30
5
Microscopically consists of an overgrowth of fibrous, acinar and
ductal epithelial structure
Is usually 1-10cm in diameter
Is clinically firm, not attached to skin or underlying muscle but the
edge may be indefinite
May be multiple
Intracanalicular fibroadenoma:
Usually occurs in the age group 30 to 50
Is commoner than the percanalicular type
When cut across looks like cysts enclosing cauliflower-like masses
Microscopically shows delicate proliferating connective tissue most
dense around the ducts
Rarely becomes sarcomatous
Intracanalicular fibroadenoma:
May be up to about 10cm in diameter and occupy most of the
breast
Is soft
Has nodular surface
Is mobile
Is well encapsulated and not attached to skin, surrounding breast
tissue or underlying muscle
Cystosarcoma phylloides:
Is pathologically different from fibroadenoma
Grows slowly but attains a large size, up to 30cm in some patients
Is multicystic with papillary growths extending into the cysts
Does not become malignant
Is seen usually in women between 20 and 30
In cystosarcoma phylloides:
The subcutaneous veins are distended and the skin stretched over
it
The skin may ulcerate
The edges are definite and there is no attachment to underlying
muscle, surrounding tissues or skin
The surface is lobulated and solid and cystic areas can be felt
The treatment is simple excision
Duct papilloma:
A Arises from the epithelium of an acinus
B. May become malignant
C. Presents commonly with recurrent bleeding from the nipple or a
swelling
6
D. Is usually seen in patients between 20 and 50
E. Is best treated by simple mastectomy
Epidemiologically, the risk in a woman developing carcinoma of
the breast is increased by:
7
Is very cellular with little stroma
Is densely infiltrated with lymphocytes and plasma cells
Has a poor prognosis
In EARLY carcinoma of the breast, the lump:
Is hard and small
Has definite edges
May be attached to the skin
Is not attached to the underlying muscle
Is associated with retracted nipple
In Paget’s disease of the breast:
There is eczema-like excoriation of the areola and nipple
The nipple may be eroded
There is usually a palpable lump in the breast
The nipple is retracted
Axillary lymph nodes are usually palpable
“A 50year old woman presented with a swelling, 2cm in diameter, in the upper
lateral quadrant of the right breast. There was no attachment to skin or
underlying muscle and the nipple was not retracted. A solitary axillary lymph
node was palpable. Extended simple mastectomy was done following a core
biopsy. The axillary nodes were histologically free of metastases. No distant
metastases were detected.
8
Stage 1
Stage 2
Stage 3
Stage 4
Investigations to be done in clinically established early carcinoma
of the breast where all facilities exist include:
9
Sternal part of pectoralis major
Clavicular part of pectoralis major
Axillary lymph nodes and fat
Structures removed in extended simple mastectomy include:
Breast
Pectoralis minor
Sternal portion of pectoralis major
Clavicular portion of pectoralis major
Axillary lymph nodes and fat
10
In the response of carcinoma of the breast to hormonal therapy:
Response of patients with primary tumours with oestrogen or
progesterone receptors is 60%
The shorter the interval between treatment of the primary disease
and the appearance of metastases the better the response.
Visceral deposits are more likely to regress than osseous deposits
Premenopausal patients respond best and menopausal patients
worst
A patient who has not responded to the first line of hormone therapy
is more likely to response to the second line
Radiotherapy in the treatment of carcinoma of the breast:
Is of proven value in early cases and improves the overall survival
rates
Reduces the incidence of local recurrence and has same effect on
subsequent development of distant metastases
Alleviates pain in advanced cases or local recurrence or bony
deposits
Is beneficial for treating fungating or ulcerating tumour
Does not depress immunity
Substances being tried or used for non-specific immunotherapy
in cancer include:
B.C.G. vaccine
Corynebacterium parvum
Autograft of irradiated cancer cells
Levamisole
Inteferon
Multiple fibroadenomata
Carcinomatous deposits
Fibroadenosis
Burkitt’s lymphoma
11
Lymphoma
A nipple discharge which is clear, creamy, green, brown or black
without red cells is associated with:
Duct estasia
Duct papilloma
Benign mammary dysplasia
Galactorrhoea
Medullary carcinoma
A bloody nipple discharge may be caused by:
Duct estasia
Intraductal comedo-carcinoma
Breast abscess
Scirrhous carcinoma
Paget’s disease
A purulent nipple discharge may be caused by:
Benign mammary dysplasia
Breast abscess
Traumatic fat necrosis
Duct ectasia
Leiomyosarcoma
The discharge should always be examined for red and pus cells
and cancer cells and microorganisms
If the discharge is blood-stained, the patients should be followed up
monthly and a biopsy done if it does not stop in 3 months
If the discharge is not blood-stained and it does not stop
spontaneously, then a biopsy should be done.
If the patient is less than 40 and the discharge is not blood-stained
but persists, a biopsy is not essential
A course of antibiotics is beneficial
A 4 cm non-tender soft, rather fluctuant, lobulated mobile swelling
with definite edges and no attachment to skin or muscle in a
12
normal breast in a 45-year old woman is mostly likely:
Early carcinoma
Chronic abscess
Galactocele
Cyst of benign mammary dysplasia
Lipoma
A firm non-tender discrete 3 cm lump with indefinite edges and no
attachment of skin or pectoralis muscle nor associated retraction
of the nipple in the ‘lumpy’ breast of a 45-year old woman may be:
13
Methyldopa
The commonest cause of swelling in the adult male breast is:
Gynaecomastia
Firboadenosis
Lipoma
Sebaceous cyst
Carcinoma
Carcinoma of the male breast:
Accounts for about 1% of all male cancers and about 2% of all
breast cancers
May present with serous or serosanguinous nipple discharge
Is best treated by mastectomy followed by irradiation if the axillary
lymph nodes are involved.
If advanced always responds to orchidectomy or oestrogens
Has a worse prognosis than in women.
In Carcinoma of the breast in West Africa:
Most patients are between the ages of 35 and 50
The risk of a breast lump being malignant is higher in a 66 year old
than a
36 year old woman
About 65% have advanced disease
Tamoxifen will be effective adjuvant treatment in the majority of
patients
The incidence is rare below age 20
Cancer of the breast:
Is estimated to affect about 1 million women worldwide annually
Affects 1 in 10 women in Africa their lifetime
Is second only to cervical cancer in incidence worldwide
Accounts for about 15% of all cancers in Accra
Has a high incidence in Japan
In this patient:
14
The pathological staging is T1N2Mx
The tumour is poorly differentiated
Chemotherapy will be useful
A FISH test is necessary
Hormonal therapy using Anastrozole is indicated
In the treatment of this patient:
15
In the hormonal treatment of carcinoma of the breast:
A patient who has had her ovaries removed will further benefit from
the Aromatase inhibitor anastrozol
Most recurrences occur within the first year, but some occur as long
as 15-20
years after treatment:
For the histological type, stage and age of patient, Caucasians and
Blacks have the same prognosis
16
A. Mammography is important even when the diagnosis is ‘obvious’
17
to occur at this time
Fever with an absolute neutrophil count (ANC) of 0.9 is an
oncological emergency
50% dose reduction for the subsequent cycles is indicated if the
patient has an ANC of 0.8 on the 10th day following chemotherapy.
Features that suggest malignancy in a patient with a breast lump
are:
CHAPTER 28
THE BREAST
B, C, D E 36. C 71. C
C, D 37. B, C, E 72. A, B
A, C, E 38. A, B, C, D 73. A, C,
18
E
C 39. A, D 74. A, B
B, D, E 40. A, B 75. B, C,
D
A, C E 41. C, E 76. A, B,
C, E
B 42. D 77. A, C,
E
B, D, E 43. B 78. A, B,
D
A, C, D 44. A, B, C 79. B, D,
E
A, C, D 45. B, C, D 80. D
E 46. B, E 81. D
C, E 47. B, C, D 82. B, D
A 48. A, B, C, E
B, C, D 49. A, E
E 50. D, E
A, D, E 51. B, C, D
A, B, C, E 52. B, D
A, D, E 53. A
A, B, C, D, E 54. C, D
A, B, C, D, E 55. A, B, D, E
C 56. B
C, D 57. A, D, E
B, C 58. A, C
19
A, C, E 59. B
A, C 60. B, D
B, C 61. C
A, B, C, D, E 62. E
B, E 63. A, C, D, E
A, C, E 64. B, C
A, B, D, E 65. A, B, C, D
B, C 66. A, B, C, D, E
A, B, C, D 67. A
B, C 68. B, C, E
A, D, E 69. A, B, C, E
B, E 70. A, D
20
CHAPTER 29
1
Oblique
Upper transverse
2
May damage the lilio-inguinal and illiohypogastric nerves
Is at right angles to the spino-umbilical line two-thirds up from the anterior
superior iliac spine
Divides the external oblique aponeurosis at right angles to the line of its
fibres
3
Splenic abscess
Portal vein thrombosis with concomitant prehepatic portal hypertension
Umbilical sinus formation
4
is 84/min, BP 140/90 and temperature 37.70C. There is an area of
localized tenderness in the ® lower quadrant with guarding and a vogue
mass is discernable. The most likely diagnosis is:
Abruptio placenta
Acute degeneration of uterine fibroids
Acute appendicitis
Rapture of inferior Epigatsric Artery
Twisted ovarian cyst
CHAPTER 29
A, C, D
B, D, E
B, E
A, C
A, C, E
A, D, E
C, E
B, C
A, D
B, C
A, D, E
A, C
A, B, C, E
B, E
A, C, E
B, D, E
A, D
C
C
D
E
D
5
CHAPTER 30
HERNIA (EXCLUDING DIAPHRAGMATIC HERNIA)
A hernia:
Is the protrusion of a viscus or part of it from the cavity in which it is
enclosed.
Is the commonest condition encountered in general surgical practice.
Afflicts about 10% of a community
Is the commonest cause of intestinal obstruction in Black Africa
Accounts for about 40% of cases of intestinal obstruction in Ghana.
Concerning hernia:
An inguinal hernia accounts for 95-97%
A femoral hernia is a hernia through the femoral sheath
A spigelian hernia is a hernia through the internal oblique
A paraumbilical hernia is a hernia through the blinded linear alba in the
umbilicus
An epigastric hernia is a hernia through the linear alba midway between
the xiphisternum and the umbilicus.
1
Bladder
Appendix
2
hernia
The testis:
Develops from the genital ridge in the posterior abdominal wall lateral to
the developing kidney
Lies in the iliac fossa near the internal inguinal ring from the second to the
seventh month of intra-uterine life
Has traversed the inguinal canal by the 8th month and is at the external
inguinal ring
Descends into the scrotum in the 9th month
Descends later on the right than on the left and in about 10% of infants
descent is not complete at term.
3
Failure of obliteration of the processus vaginalis may lead to:
Indirect inguinal hernia in infacts but not in adults
Encysted hydrocele of the cord
Infantile or congenital hydrocele
Vaginal hydrocele
Cyst of the canal of Nuck
A 5-year old boy has a scrotal swelling extending from the right half of
the groin. It is soft, fluctuant and irreducible; there is no obvious cough
impulse and the testis is impalpable.
A 20-year old man has a tense fluctuant ovoid swelling without a cough
impulse in the left groin which moves with traction on the testis.
4
The most likely clinical diagnosis is:
Sebaceous cyst
L.I.H. – irreducible, incomplete and probably containing omentum
Encysted hydrocele of the cord
Cyst of the epididymis
Lipoma
Tanner slide:
Is separation of the attachment of the external oblique oponeurosis from
the rectus sheath
Is an incision in the transversalis fascia in the triangle of Hesselbach
Is an incision in the anterior rectus sheath close to the attachment of the
external oblique aponeurosis
Is an incision in the conjoint tendon
5
Relieves tension on Bassini repair
Femoral hernia:
Is as common in Black Africa as in Europe
Is five times commoner in females
Is more common in the multiparous than in the nulliparous
Occurs in all age groups
In Ghanaian males is commoner than umbilical hernia
6
Weakening of the femoral sheath by the presence of the femoral vein and
artery
A femoral hernia:
Is usually below and lateral to the pubic tubercle
May lie in front of or above the inguinal ligament
Has a visible and palpable cough impulse in every patent unless it is
strangulated
May not disappear when the patient lies down
Commonly contains small intestine, bladder, colon or appendix and
occasionally omentum
A 40-year old woman has a 2-year old lump in the right groin, below and
lateral to the pubic tubercle and with doubtful cough impulse. It
disappears as soon as the patient lies down and elevates her leg above the
trunk. The most likely clinical diagnosis is:
Femoral hernia
Encysted hydrocoele in a femoral hernial sac.
Saphena varix
Femoral aneurysm
Psoas abscess
Femoral hernia:
Can be adequately controlled by a truss
Is more liable to strangulation than any other hernia
Is most commonly strangulated by the lateral edge of the lacunar ligament
May be strangulated at the saphenous opening
May be strangulated by the neck of the sac or by the defect in the
transversalis fascia
7
Recurrence after femoral herniorrhaphy is:
5-10%
10-20%
20-25%
25-30%
About 35%
Exomphalos:
Occurs in 1 in 6,000 births
Is major if it is large
Is minor if it is small
Has associated congenital anomalies such as heart disease, cleft palate and
intestinal atresia in about 80% of patients
Is associated with non-rotation of the gut in about 25% of patients who
frequently are premature
In exomphalos major:
The causes are failure of development of the abdominal cavity and non-
rotation of the bowel
The hernia sac is translucent and jelly-like and consists of amnion,
Wharton’s jelly and peritoneum
The umbilical cord is attached to the superior border of the sac
The sac contains spleen, the transverse colon, and stomach and at times
small intestine as well.
The defect in the abdominal wall is always large
In exomphalos minor:
The cause is incomplete return of the midgut from the umbilicus to the
abdominal cavity
The hernia contains a loop of small intestine
The defect is small
The umbilical cord is attached to the midpoint
Treatment is always operative
8
May be predisposed to by umbilical sepsis
Is commoner in premature infants
Is commonly irreducible
Is treated by Mayo’s overlapping operation in most patients
Paraumbilical hernia:
Is more common in multiparous obese women
Usually has a narrow neck
May rupture
Can be satisfactorily controlled with an abdominal belt in most patients
If treated by operation has a negligible recurrence rate.
Epigastric hernia:
Occurs commonly in all age groups but especially in those between 20
and 50
Is equally common in the sexes
May be multiple
Is a protrusion of extra-peritoneal fat in a few but in the majority has a true
hernia sac.
Usually has a small defect, about 1cm or less, through the linea alba.
Epigastric hernia:
Causes epigastric pain or discomfort in most patients
Always has a cough impulse but it may not be reducible
Rarely strangulates
Should be left alone if symptomless
Has a recurrence rate of 1% after operative repair
Incisional hernia:
Has a wide and not a narrow neck
May not have a sac
Does not strangulate
May rupture
Should be repaired in every patient if possible
Spigelian hernia:
Usually occurs in the elderly
Often causes localized pain, worse on coughing or straining and relieved
9
by lying down
Usually appears medial to the lateral border of the rectus
Spreads downwards and laterally or upwards and laterally
May be strangulated by the cresentic rigid defect
Obturator hernia:
Is commoner in males and on the right
Is usually seen in the middle-aged between 40-50
Usually presents with acute intestinal obstruction
Causes referred pain or paraesthesia along the posterior part of high or
knee
Is always treated by operation.
Lumbar hernia:
Is commoner in males
Is usually seen in people between 50 and 70
May be confused with or cold abscess
Is acquired but may very rarely be congenital
Need not be repaired
In Linchtenstein repair
The mesh is placed over the inguinal floor between the inguinal ligament
and the conjoint tendon.
When the mesh becomes incorporated, tissue collagen grows into it.
In tension-free repair,
10
There is early return to work
Recurrence is reduced.
In the repair there is the need to tighten the deep inguinal ring around the
spermatic cord.
Repair of the posterior wall should be done in those from the age 6 years.
In Bassini repair the most medial stitch should pass through the
periosteum of the pubic tubercle.
In nylon darn repair the gap between the inguinal ligament and the
conjoint tendon is re-enforced with 2 layers of monofilament nylon.
11
Laparoscopic repair is not suitable for bilateral inguinal hernia.
12
CHAPTER 30
A, B, D
A
C
A, B, C, D
B, C, E
B, D
A, C
C, E
D
A
A, C
C
C, E
A, C, D, E
C, D, E
B, C, E
B, C, E
A
C, D, E
A, B
D, E,
C
B, D
A, B, C
A
B, D
C, E
A, D
B, C, E
A, B, C
A, B, C
C
B, C
A, B, D
13
A, C
B, C, E
A, C
B
A, E
A, B
A, B, C, D, E
B,C, E
B, C
A, C, E
C, E
C, D
A, B, C, D
B, D
A, B, D, E
C, E
A, B, C, D
A, B, C, D, E
B, C, E
A,B,C,D,E
B, C
B,C,D,E
A,B,C
A, D, E
C
A, D, E
14
CHAPTER 31
THE ACUTE ABDOMEN
A. Acute gastritis
B. Gastric outlet obstruction
C. Gastro-enteritis
D. Acute high intestinal obstruction
E. Acute pancreatitis
A. Bacillary dysentery
B. Intussusception
C. Amoebic dysentery
D. Cholera
1
E. Ankylostomiasis
A. Bacillary dysentery
B. Ulcerative colitis
C. Acute appendicitis
D. Amoebic dysentery
E. Cholera
A. Cervicitis
B. Pelvic inflammatory disease
C. Gonorrhoea
D. Trichomonad vaginitis
E. Endometritis
A. Malaria
Acute appendicitis
C. Typhoid perforation
D. Amoebic perforation
E. Perforated duodenal ulcer
2
conjunctivae and hypotension should immediately raise a
suspicion of:
If in a 30-year old man with acute abdomen, you observe that the
abdomen does not move on respiration, you will suspect:
3
C. Rupture of abdominal aortic aneurysm
D. Mesenteric thrombosis
E. Strangulated internal hernia
4
not entered the peritoneum
D. Turbid, the diagnosis is probably peritonitis
E. Nil, there is probably nothing serious in the abdomen
A. Pre-diabetic coma
B. Acute pancreatitis
C. Acute abdomen in a diabetic
D. Urinary tract infection
E. Viral hepatitis
A 12-year old West African boy known to suffer from sickle cell
disease has a 24-h history of persistent pain in the R.I.F. which
started around the umbilicus. There is nausea but no vomiting.
There are no bowel or urinary symptoms and no joint aches. On
examination, the conjunctivae are moderately pale, the tongue
slightly furred, the temperature 38oC and the pulse 100/min. There
is marked tenderness in the R.I.F. with guarding rebound
tenderness. Rectal examination is unremarkable.
A. Sickle-cell crisis
B. Acute appendicitis
C. Mesenteric adenitis
D. Right iliac adenitis
E. Malaria
5
You will advise:
A. Observation
B. Paracetamol
C. Paracetamol and artesunate + amodiaquinel
D. Immediate appendicectomy
E. Antibiotics
A 15-year old Ghanaian boy has for the past 3 days been having
headache, malaise, evening pyrexia and pain especially in the
R.I.F. He has been vomiting on and off but has not been
constipated. There is some frequency but no dysuria. On
examination, the temperature 39oC and the pulse 108/min. The
conjunctivae are pink and the tongue clean. The abdomen is soft
with slight tenderness in the R.I.F without guarding. Rectal
examination is unremarkable.
A. Acute appendicitis
B. Enteric fever
C. Sickle cell disease
D. Urinary tract infection
E. Malaria
6
C. Blood film
D. Urinalysis
E. Sickling
A. Appendicectomy
B. Ciprofloxacin + metronidazole
C. Paracetamol
D. Artesunate + Amodiaquine + Paracetamol
E. Septrin
7
tenderness and rigidity especially in the epigastrium. Bowel
sounds are infrequent and rectal examination is tender.
A. Serum amylase
B. 4-quadrant paracentesis
C. Full blood count
D. Widal
E. Straight X-ray of the abdomen and chest in the erect position
A. Glucagon I.V.
B. Intravenous fluid therapy
C. Nasogastric decompression
8
D. Observation
E. Antibiotic therapy
9
vesical pouch and no blood or mucus on the finger.
A. Intussusception
B. Gastro-enteritis
C. Typhoid perforation
D. Peritonitis from amoebiasis
E. Acute appendicitis
A. Myocardial infarction
B. Glomerulonephritis
C. Malaria
D. Meningitis
E. Herpes zoster
10
The clinical features of acute pancreatitis include:
In biliary colic:
In ureteric colic:
11
E. The patient may be restless
In myocardial infarction:
A. The pain is in the precordium and may radiate down the left arm
B. The upper abdomen is tender and guarded
C. The abdomen is silent
D. Cardiac signs are present
E. The diagnosis is usually established with E.C.G. in doubtful cases
In salpingitis:
In gastroenteritis:
12
In right basal pneumonia in children:
CHAPTER 31
THE ACUTE ABDOMEN
ANSWERS
A, C, E
D
B
13
A, D
B, C
A, C
E
B, D
B, C
E
A, C,D, E
A, B, D
A, B, C
B
D
E
A, B, C, D, E
D
B
E
A, C, D
B, C, E
A, C
C
A, B, D
A, C, E
A, C, E
A, C
B, C, E
14
A, D, E
A, B, C, D, E
C, E
A, D, E
15
CHAPTER 32
PERITONEAL CAVITY
The peritoneum:
Has about the same surface area as the skin, approximately 1.8m2
Is semi-permeable
The space is divided into right and left compartments by the falciform
ligament
The falciform ligament sweeps from the diaphragm and back of the linear
alba as far down as 2cm below the umbilicus
The coronary ligament suspends the liver superiorly from the diaphragm
and divides the subphrenic space into anterior and posterior parts
The right subphrenic space communicates with the subhepatic space and
general peritoneal cavity
On the right is continuous posteriorly with the upper part of the right
paracolic gutter and communicates anteriorly with the right sub-phrenic
space and the general peritoneal cavity
On the right is a more common site of abscess formation than the sub-
phrenic space
1
The epiploic foramen to the lesser sac (foramen of Winslow) is:
Bounded anteriorly by the common bile duct, hepatic artery and portal
vein
The inferior ileo-caecal recess between the inferior surface of the terminal
ileum, the meso-appendix and the triangular ileo-caecal fold
Caudate lobe
Lesser omentum
Stomach
Transverse colon
Transverse mesocolon
Primary peritonitis:
Is uncommon
2
Is seen in boys and girls between 4 and 10
Hepatitis
Septicaemia
Amoebic colitis
Enteric fever
Strep. Haemolyticus
Pseudomonas
Staph. Epidermidis
Bacteroides
Clostridia
3
The pathological processes in acute generalized peritonitis include:
Vascular constriction
Rupture of capillaries
Matting of viscera
Vit. C deficiency
There is loss of large amounts of plasma, 4-6L, into the peritoneal cavity
There is loss of E.C.F. into the loss connective tissues of the peritoneum
The rapid absorption of toxins and bacteria from the peritoneum in acute
generalized peritonitis is due to:
Paralytic ileus
4
Semi-permeability of the peritoneum
Respiratory alkalosis
Metabolic acidosis
Hypoproteinaemia
Hyperchloraemia
Hypocalcaemia
Respiratory failure
Cerebro-vascular accident
Septicaemia
Intermittent
Severe
Burning in character
In generalized peritonitis:
5
Copious persistent vomiting is the rule
A careful history will often indicate the site of origin of the pain
Rapid
Deep
Grunting
Stertorous at times
Irregular at times
Is not distended
On auscultation at times gives rise to only audible heart and breath sounds
6
In acute generalized peritonitis, the primary condition is most probably:
Malaria
Strangulation obstruction
Acute dysentery
Blood transfusion
Relief of pain
7
Acute diverticular disease
Acute cholecystitis
Amoebic colitis
Puerperal sepsis
Moribund patient
Localization of abscess
Associated hypertension
Bile peritonitis:
8
Sites of intra-peritoneal abscess include the:
Lesser sac
Subhepatic space
Paracolic spaces
Paraduodenal recess
Ten days after closure of typhoid perforation, a 20-year old man develops
pain in the right upper abdomen, cough and a swinging temperature.
There is tenderness in the right upper abdomen over the liver between the
ribs. A few crepitations are heard over the right lower lobe.
Rt. Empyema
Liver abscess
Liver biopsy
Sputum culture
Antibiotics
9
Antibiotics and aspiration
Empyema
Liver abscess
Peritonitis
Septicaemia
Elevated diaphragm
Settles on antibiotics
10
A pelvic abscess:
In the female is located mainly between the bladder and the uterus
Surgical site infection can be reliably identified from laboratory data alone
11
Iatrogenic perforation of a hollow viscus is another cause.
Selective use of CT scan in patients presenting with right lower quadrant pain
is helpful in reducing the incidence of non-therapeutic appendectomy.
12
CHAPTER 32
A, D
A
B, C,E
B, D, E
C, E
A, B, C
A, C, D
B, C, E
E
B, D, E
B, C, E
A, C, D
B, E
A, C, D
B, C
A, C, E
B, C, D
B, E
A, C
B, C, E
A, D, E
B, E
A, C, D
B, C, D, E
13
A
A, B, E
A, D, E
A, D
A, B, D
A, B
C
D
A, B, D, E
B, C, D E
A, B, D
A, D
C, D
A, D, E
A,B,C,D,E
B,C,D
14
CHAPTER 33
THE APPENDIX
The appendix:
A. Arises from the medial aspect of the caecum about 5cm below the
ileocaecal
junction
The appendix:
1
propensities
C. May lead to pseudomyxoma peritonei
D. Present with pain in the R.I.F. or a palpable mass
E. Be calcified
In pseudomyxoma peritonei:
2
The incidence of acute appendicitis:
A. Low residue
B. Short transit time
C. Formation of firm and tenacious faeces
D. Development of low intra-luminal pressure
E. Formation of faecoliths
A. Ova of schistosoma
B. Lymphoid hyperplasia
C. Hypertrophy of the muscular layer
D. Fibrous adhesions in the lumen
E. Serosal adhesions and kinking
3
D. Luminal obstruction
E. Salpingitis in the female
Acute appendicitis:
4
Usual causes of perforation or gangrene of the appendix in acute
appendicitis include:
A. Subhepatic abscess
B. Pylephlebitis or liver abscess
C. Mesenteric arterial thrombosis
D. Cholangitis
May be colicky
May radiate from the right iliac fossa to the centre of the abdomen
May improve for some hours only to become more severe later
In acute appendicitis:
5
C. Diarrhea occurs in about 20% of patients especially in the young
D. Frequency and dysuria may occur
E. There is pyrexia with associated tachycardia from the beginning of
the attack
A. Rebound tenderness
Guarding
C. Typical “appendiceal foetor”
D. Pain on flexing the right hip
E. Localised tenderness over the appendix
6
B. In the first two trimesters may pose diagnostic problems
C. In the third trimester gives rise to pain in the right upper abdomen
and rather
laterally
D. In the third trimester causes marked muscle guarding
E. In the third trimester causes pain which may be confused with labour
pains
A. Acute cholecystitis
B. Left basal pneumonia
C. Malaria
D. Non-specific mesenteric adenitis
E. Ruptured Graafian follicle
A. Most commonly occurs from the spread of infection from the serosal
surface of
the appendix to the visceral and parietal peritoneum
7
caecum,
omentum, coils of terminal ileum and the sigmoid colon
B. Is seen in patients with average duration of symptoms of 7-8 days
C. Nearly always proceeds to suppuration
D. Is proportionately less common after 40 years
E. Is difficult to differentiate from a appendix abscess
A. Amoeboma
8
B. Ileo-caecal tuberculosis
C. Carcinoma of the caecum
D. Pyomyositis of the anterior abdominal wall
E. Right hydronephrosis
9
diarrhea.
Pelvic peritonitis
In pyeliphlebitis:
10
There may be subsequent liver abscesses
A tender mass in the R.I.F. in a 45-year old man is found in two
weeks to be half its size. There is no further reduction in size
during the next three weeks.
11
The treatment of appendix mass /abscess is:
A. Presence of a mass/abscess
B. High temperature and tachycardia
C. Absence of guarding or rebound tenderness
D. Settling inflammation as shown by decreasing pain and tenderness
and near
12
normal pulse
E. Associated sickle cell disease
13
C. An analgesic such as pethidine should be administered 6-8 hourly
D. The mass should, if possible, be examined twice daily and its size
and degree
and distribution of pain and tenderness observed
E. Intravenous fluid therapy is essential in all cases
14
C. There is pus around the appendix
D. There is localized peritonitis without pus formation
E. The appendix is pelvic in position
A. Haemorrhage
Paracaecal abscess
C. Paralytic ileus
D. Generalized peritonitis
E. Wound infection
Acute appendicitis:
15
In obstructive acute appendicitis:
A. Spontaneous resolution
16
Recurrent acute attacks
In acute appendicitis:
A. Anorexia is invariable
B. The pain may start in the R.I.F. and not the centre of the abdomen
C. Bowel function is usually normal
D. Boas’s sign may be positive
E. The psoas sign may be positive
17
D. Herpes Zoster
E. Sickle Cell crisis
In appendix mass:
18
CHAPTER 33
THE APPENDIX
ANSWERS
B, C 34.A, D
19
D 35.B, C, D
A, B, C, D, E 36. A, D
D 37.B, D
A, D 38. A, D
C, E 39. B, C
A, C, E 40. E
A, B, D, E 41.A, B, C, E
A,C, D 42.A, B, D, E
B 43.C,D
A, C 44. A, B, C, D, E
B, D, E 45. A, B, E
A, B, E 46. A, D
B, C 47. A, B, C, D, E
C, D 48. A, B, C, D, E
E 49. A, D, E
A, B 50. A, C, D
C, E
C, D
B, E
A, B, E
B, C
A, B, C, D, E
A
B, C, D, E
20
A, C, D, E
B
D
B, C, D, E
E
D
B
D
21
CHAPTER 34
ACUTE INTESTINAL OBSTRUCTION
A. A simple obstruction
B. A strangulation obstruction
C. A closed loop obstruction
D. The commonest cause of intestinal obstruction in women in West
Africa
1
A. Is raised by gases and intestinal secretions
B. May be 10mmHg in small bowel obstruction
C. May be 25mmHg in large bowel obstruction
D. Causes outpouring of fluid from the plasma into the lumen of the gut
and
peritoneum
E. Does not affect the blood supply
2
Death from simple occlusion intestinal obstruction is due
primarily to:
A. Peritonitis
B. Loss of water and electrolytes
C. Renal failure
D. Respiratory failure
E. Septicaemia
In a strangulated hernia:
A. Peritonitis
B. Loss of water and electrolytes
C. Shock
D. Renal failure
3
E. Septicaemia
4
A. Ileal contents entering the caecum
B. Swallowed air
C. Fermentation of contents by bacteria
D. Diffusion of air from the plasma
E. Exudation of water and electrolytes from the plasma
In intestinal obstruction:
A. Kanamycin
B. Ciprofloxacin
5
C. Ampicillin
D. Metronidazole
E. Gentamicin
A. Terminal ileum
B. Transverse colon
C. Sigmoid colon
D. Jejunum
E. Rectum
6
A. The nature of obstruction is important
B. The cause of obstruction per se is not important
C. Low obstruction has a worse prognosis than high obstruction
D. Resection does not significantly raise the mortality
E. The child has a better chance than the young adult
In black Africa:
Richter’s strangulation:
A. Is when in a big hernia, two loops of bowel in the sac as well as the
intervening loop in the abdomen are strangulated
B. Is more common in strangulated femoral hernia
C. May not be associated with constipation
D. May, if untreated, lead to entero-cutaneous fistula
E. May not be associated with vomiting
7
In a strangulated hernia containing small bowel:
A. Epiploic foramen
8
B. An acquired defect in the mesentery
C. Broad ligament
D. Base of sigmoid mesocolon
E. Retroperitoneal fossa at the duodeno-jejunal junction
A 60-year old woman has colicky central abdominal pain of 12h
associated with vomiting and absolute constipation. She also has
pain on the medial aspect of the left thigh.
9
Indications for laparotomy during expectant management of
simple occlusion obstruction caused by post-operative adhesions
include:
10
E. Sunken eyes, dry inelastic skin
A. Enema saponis
B. Sigmoidoscopy and passage of a rectal tube
C. Laparotomy and detorsion of the bowel of the bowel
D. Laparotomy and resection of the sigmoid
E. Sedation and use of I/V smooth muscle relaxants
11
Intussusception:
In intussusception:
12
D. The commonest type is the ileo-colic except among the Yorubas in
whom the
caeco-colic is the commonest
E. The intusscepting bowel does not reach the anus
In intussusceptions:
A. Adenoma
B. Leiomyoma
C. Carcinoma
D. Lipoma
E. Intestinal polyposis
Intestinal obstruction:
13
sigmoid
colectomy
The straight X-ray of the abdomen of a 10-year old boy shows air-
fluid levels mainly in the central part. There are also translucent
entangled lines in the right lower part.
A. Intussusception
B. Faecal impaction
C. Intestinal obstruction by foreign bodies
D. Intestinal obstruction by ascaris lumbricoides
E. Intestinal obstruction of unknown cause
14
The most likely clinical diagnosis is:
A. Intussusceptions
B. Myocardial infarction
C. Mesenteric vascular occlusion
D. Strangulation obstruction of unknown cause
E. Ruptured aortic aneurysm
Uraemia
A. Nasogastric decompression
B. Purgation
C. Soap and water enema
D. Intravenous fluids and electrolytes
15
E. Laparotomy
A. Guanethidine
B. Neostigmine
C. Adrenaline
D. Propranolol
E. Chlorpromazine
Intestinal atresia:
16
gestation
E. Is associated with other major malformations in most patients
Meconium ileus:
A. Abdominal distension
B. Vomiting which is always bilious
C. Failure to pass meconium in 36 hours
D. Oedema of the abdominal wall
17
In acute intestinal obstruction:
18
Release of the obstruction in strangulation obstruction may lead to
severe
endotoxic shock
CHAPTER 34
ACUTE INTESTINAL OBSTRUCTION
ANSWERS
19
C, D 40. B,C
A, B, C 41. A,D
B 42. A, B, E
A, B, C, D 43. A, B, E
A, B, C 44. B, C, D
B 45. D
A, B, C 46. A, C
A, D 47. A, B, C
C 48. C
C 49. A, B, D
B 50. B
C
C, D
A, B, C
B, D
B, D
B, C, E
A
A, D
A, B
B, C, D
A, D, E
B, C
A, B, C, D, E
20
D
A, B, C, D
A, C, D
A, C, D
B, E
B, D
A, B, C, D
B, C, E
C, D
B, C
D
B, C, D
D
C
A, C, D, E
21
CH
APT
ER
35
A. N. gonorrhea
B. Esch. coli
C. Chlamydia trachomatis
D. Streptococcus
E. Staph. aureus
1
3. Acute salpingitis may follow:
A. Laparoscopy
B. Insertion of I.U.D.
D. Hysterosalpingography
E. Normal delivery
4. In gonorrhea:
B. Infection spreads from the cervix to the uterine tubes via the lymphatics
and blood vessesls
C. Pelvic periotonitis follows leakage of exudates from the tubes via the
lymphatics and blood vessles
C. The endometrium is rapidly infected directly from the cervix but the infection is
transient
5. After abortion:
2
6. Acute salpingitis:
A. Is the commonest cause of peritonitis in the female
in West Africa
7. In gonococcal salpingitis:
8. In post-abortal salpingitis:
3
9. Clinical features of acute salpingitis
include:
B. ES.R.
D. Urethral swab
E. Blood culture
4
A. Perforated duodenal ulcer
B. Cystitis
D. Acute appendicitis
A. Intestinal
obstruction
B
Pyelonephritis
C. Tubal
pregnancy
D. Renal
failutre
E. Ovarian
A. Bed rest
B.
Administration of
analgesics
C.
Administration of
antibiotics
5
D. Vaginal
douches
E. Laparotomy
14. Ectopic
pregnancy:
A Previous
tubal reconstruction
C. Oligomenorrhoea
D. Leucorrhoea
6
16. Aetiological factors in ectopic
pregnancy include:
B. Previous
puerperal sepsis
C. Myomata
uteri
D. Ovarian cyst
E. Recurrent
urinary tract
infection
17. In ectopic
pregnancy:
18. Following abortion of the embryo into the lumen of the tube in tubal
pregnancy, there
may be:
7
A. Incomplete
abortion
B. Complete
abortion
C. Absorption of
the ambryo
D. Tubal mole
formation
E. Peritubal or
pelvic haematocele
19. Rapidly fatal heavy and prolonged haemorrhage usually follows rupture
of:
A. Ovarian
pregnancy
B. Interstitial
pregnancy
C. Fimbrial pregnancy
D. Isthmial pregnancy
E. Ampullary pregnancy
B. Sudden severe camping pain which starts in the hypogastrium or an iliac fossa
and becomes
generalized
8
E. Exquisiste tenderness in the affected fornix on bi-
manual examination.
A. Retention of urine
B. A normal uterus
E. A history of collapse
9
B.
Culdocentesis
C. Pelvic examination
under anaesthesia
D. Laparoscop
y of the
pelvis
E. Curettage
A.
Salpingostomy
B.
Salpingectomy
C. Partial
salpingectomy
D.
Salpingo-
oophorectomy
E.
Salpingo-
hysterectomy
A.
Retention of
urine
B.
Intestinal
Obstruction
10
C. Urinary
tract infection
D. Pelvic
abscess
E. Acute
renal failure
8. 4 weeks
C. 6 weeks
D. 8 weeks
E. varies with location
11
29. Spielgelberg's criteria for ovarian pregnancy exclude:
A. An inteact fallopian tube
B. An ovary of normal position
C. Ovarian tissue in the wall of gestational sac
D. A fallopian tube connected to the uterus by the ovarian ligament
E. Normal Fimbrial ovarica
A.
Clinica
l
suspici
on
B.
Cervic
al
gram
stain
C.
Anaer
obic
Cultur
e
D. While cell
count less than
800
E.
12
Reboun
d
tendern
ess
A. A
recurrent
vulvar
growths
B. Cyclic
migratory
arthralgia
C. Involuntary infertility
D.
Vagini
smus
E.
Endoc
13
arditis
B. 10-15%
C.
20-
40%
D.
60-
80%
E.
Greate
r than
90%
A.
1-2
days
B. 3-5
d
a
y
s
C. 6-7
d
a
y
14
s
D. 8-
1
0
d
a
y
s
E.
More
than 6
weeks
35. The most frequent site of infecetion with gonorrhea in women is the
A. Bartholin's glands
B. Skene's glands
C Cervix
D. Urethra
E Rectal crypts
KEY
. 1. E
2. A,B,C,D,E
3. B,C,D,E
4. C,D
5. C
6. A
7. C,D,E
8. B,C
9. A,E
10. C
11. A,B,C,D,E
12. A,C
13. A,B,C 15
14. B,D,E
15. A,B,E
16. B,C,D
23. D
24. A,C,D
26. E
27. B
~
A
28.
29. D
30. B
31. A
32. C
33. C
34. B
35. C
16
CHAPTER 36
PERITONEUM, OMENTUN, MESENTERY AND
RETROPERITONEUM
Ascites:
Gives rise to fluid thrill and localized dullness of the abdomen which
is persistent even when the patient changes his position
Contains leucocytes
Is protein-rich
Is frothy as aspirated
1
Hyperaldosteronism
Hypoproteinaemia
Retention of sodium
Nephrotic syndrome
Abdominal tuberculosis
Abdominal tuberculosis
Lymphoma
2
Increased flow of lymph in the hepatic hilar lymphatics
Hyperaldosteronism
Hypoglobinaemia
be due to:
Carcinomatosis peritonei
Abdominal tuberculosis
due to:
Malnutrition
Constrictive pericarditis
3
support a diagnosis of:
Ovarian carcinoma
Meig’s syndrome
Tuberculous peritonitis
E coli peritonitis
Chronic salpingitis
Pseudomyxoma peritonel:
4
with saline followed by instillation of mycomycin C
Ovarian cyst
5
Omental cyst
Pancreatic cyst
Enterogenous cyst
Renal cyst
Cystoscopy
Intravenous pyelogram
Laparoscopy
Aortograpy
Torsion
Haemorrhage
Rupture
Infection
Calcification
A 50-year old woman complains of a 4-month slightly painful
abdominal mass. The mass is about 5 cm wide and 10 cm long
and located on either side of the midline about the mid-abdomen.
It is hard and immobile and has indefinite edges and nodular
surface:
It may be:
Retroperitoneal liposarcome
6
Retroperitoneal lymphoma
Retroperitoneal neurofibroma
Aortograpy
Laparotomy
I.V.P.
or hernia sac
It treated by untwisting it
7
Left hemicolectomy, stripping of the diaphragm
CHAPTER 36
PERITONEUM, OMENTUN, MESENTERY AND
RETROPERITONEUM
ANSWERS
C
A, B
8
B
A, B, D
E
A, B, C, D, E
A, C, D
A, C, E
B, D, E
C
A
A, C
A, C
B, D
D
A, C
A, B, C, D, E
C, D, E
C
C, D
A, B, C, E
9
CHAPTER 36
PERITONEUM, OMENTUN, MESENTERY AND
RETROPERITONEUM
Ascites:
Gives rise to fluid thrill and localized dullness of the abdomen which
is persistent even when the patient changes his position
Contains leucocytes
Is protein-rich
Is frothy as aspirated
1
Hyperaldosteronism
Hypoproteinaemia
Retention of sodium
Nephrotic syndrome
Abdominal tuberculosis
Abdominal tuberculosis
Lymphoma
2
Increased flow of lymph in the hepatic hilar lymphatics
Hyperaldosteronism
Hypoglobinaemia
be due to:
Carcinomatosis peritonei
Abdominal tuberculosis
due to:
Malnutrition
Constrictive pericarditis
3
support a diagnosis of:
Ovarian carcinoma
Meig’s syndrome
Tuberculous peritonitis
E coli peritonitis
Chronic salpingitis
Pseudomyxoma peritonel:
4
with saline followed by instillation of mycomycin C
Ovarian cyst
5
Omental cyst
Pancreatic cyst
Enterogenous cyst
Renal cyst
Cystoscopy
Intravenous pyelogram
Laparoscopy
Aortograpy
Torsion
Haemorrhage
Rupture
Infection
Calcification
A 50-year old woman complains of a 4-month slightly painful
abdominal mass. The mass is about 5 cm wide and 10 cm long
and located on either side of the midline about the mid-abdomen.
It is hard and immobile and has indefinite edges and nodular
surface:
It may be:
Retroperitoneal liposarcome
6
Retroperitoneal lymphoma
Retroperitoneal neurofibroma
Aortograpy
Laparotomy
I.V.P.
or hernia sac
It treated by untwisting it
7
Left hemicolectomy, stripping of the diaphragm
CHAPTER 36
PERITONEUM, OMENTUN, MESENTERY AND
RETROPERITONEUM
ANSWERS
C
A, B
8
B
A, B, D
E
A, B, C, D, E
A, C, D
A, C, E
B, D, E
C
A
A, C
A, C
B, D
D
A, C
A, B, C, D, E
C, D, E
C
C, D
A, B, C, E
9
CHAPTER 38
SMALL AND LARGE INTESTINES
(Including Rectum and Anus)
through the wall of the second part and enter the duodenum
B. The lumen widens and the circular folds of the mucosa become
smaller and less
frequent distally
1
The mesenteric vessels to the ileum are shorter but have more
arcades than those
of the jejunum
D. There are in the outer cell membrane enzymes for the digestion of
carbohydrates, polypeptides, nucleic acid and fat
E. The mucosal cells are shed every 5-6 days and originate in the
crypts of Lieberkuhn
A. The entire large intestine is about 150cm long but the taenia coli are
about
25cm shorter
2
various parts
The rectum:
Extends from the pelvi-rectal junction at the level of the first sacral
vertebra
In its lower third is related anteriorly to the uterus and vagina in the
female
3
C. The lymphatic drainage is all to the inguinal lymph nodes
C. The vagus and the nervi erigentes from S2-S2 provide the
parasympathetic supply
A. Secretin
D. Enkephalin
E. Glucagon
4
Succus entericus:
A. Has a Ph of 5-7
C. Contains lipase
E. Contains peptidases
A. Motilin
C. Enkephalin
D. Bombesin
E. G.I.P.
CCK-PZ:
5
Vaso-active intestinal polypeptide:
B. Is found in the mucosa of the stomach and small and large intestine
alkaline secretion
Enkephalins:
D. Subserve analgesia
6
Absorption of the following is by active transport:
A. Potassium
B. Sodium
C. Water
D. Magnesium
E. Fructose
A. Sodium
B. Potassium
C. Water
D. Bicarbonate
E. Chloride
About iron:
fatty acids
7
B. About 60% of fat is hydrolysed by pancreatic lipase
Faeces:
In intestinal motility:
8
the
mesenteric plexus
decreases distally
In the colon:
E. Mass peristalsis propels the faeces distally into the sigmoid colon
and rectum
9
In defaecation:
C. The pelvic floor rises with straightening of the angle between the
rectum and
anal canal
E. The anal sphincters relax and faeces are ejected through the anus
A. Pyloroplasty
B. Gastro-jejunostomy
10
C. Polya partial gastrectomy
A. Steatorrhoea
B. Early dumping
C. Late dumping
E. Macrocytic anaemia
A. Diarrhoea
D. Megaloblastic anaemia
the effluent
sodium daily
11
Some patients may develop calcium oxalate renal stones unless the
daily urine
output is
Microflora in the:
B. Entero-virus
D. Staphylococcus, yeast
Gut bacteria:
12
A. Produce vitamins especially K and B which are absorbed and
utilized
is no vomiting:
A. Crohn’s disease
B. Amoebiasis
C. Acute appendicitis
D. Shigellosis
E. Ascariasis
B. Stool culture
C. Colonoscopy
13
D. Proctoscopy and sigmoidoscopy
E. Barium enema
A 65-year old West African woman has for the past 3 months been
having
A. Ulcerative colitis
C. Parasitic nematodes
D. Malabsorption
E. Crohn’s disease
Bran:
stool weight
14
E. Is available only in tablet form
A. Aganglionic megacolon
B. Physical inactivity
C. Anal fissure
D. Diverticular disease
A. Intussuceptions
C. Entero-colitis
D. Severe ankylostomiasis
E. Juvenile polyp
15
35 years is:
B. Vascular ectasia
C. Haemorrhoids
E. Ulcerative colitis
A. Peptic ulcer
B. Crohn’s disease
C. Amoebiasis
E. Enteric fever
16
A. Passage of nasogastric tube and aspiration
C. Barium enema
E. Arteriography
The midgut:
B. Extends from the second part of the duodenum at the entrance point
of
the common bile duct to the junction of the middle and distal thirds
of the
transverse colon
C. Herniates through the umbilical opening into the umbilical sac in the
fifth
development
E. On its final return into the abdomen has rotated through an angle of
270o in
a clockwise direction
B. Exomphalos
C. Gastroschisis
D. Volvulus neonatorum
17
E. Situs inversus
A. Sub-heptic caecum
D. Ileo-umbilical fistula
E. Duodenal atresia
A. Meckel’s diverticulum
E. Urachal cyst
A. Carcinoma
18
B. Inflammation
D. Intussusception
E. Peptic ulceration
Failure of the uro-rectal septum to fuse with the blind end of the
cloaca is the
cause of the following fistula(e):
A. Recto-vaginal
B. Recto-vesical
C. Recto-urethral (male)
D. Recto-urethral (female)
E. Recto-uterine
In ano-rectal anomalies:
The low anomaly is that in which the bowel passes through the
pelvic floor
A. Anorectal agenesis
B. Covered anus
C. Ectopic anus
19
D. Rectal atresia with normal anal canal
E. Anal agenesis
A. Vulva
B. Vestibule
C. Upper vagina
D. Perineum
E. Scrotum
20
A. Oesophageal atresia
B. Sacral agenesis
C. Hydronephrosis
D. Septate vagina
E. Malrotation of the gut
B. A covered anus
C. Ectopic anus
D. Anorectal stenosis
E. Aganglionic megacolon
A lateral X-ray of a 24h neonate with the head down and the tube
centred on the
pubic symphysis:
21
Treatment will be:
B. Anal dilatation
6-12 months
In aganglionic megacolon:
and submucosal nerve plexus of the large bowel from the anus for a
variable
distance proximally
B. The rectum and lower sigmoid are affected in the majority of cases
22
A. Chronic obstinate constipation often dating from infancy
B. Frequent vomiting
Necrotizing enterocolitis:
23
Treatment of necrotizing enterocolitits requires:
B. Nasogastric decompression
C. Intravenous fluids
D. Antibiotics
E. Colostomy
B. Left hemicolectomy
D. Duhamel’s operation
E. Soave’s operation
In aganglionic megacolon:
In intestinal tuberculosis:
24
B. The infection is blood-borne
C. The mesenteric lymph nodes are the first to be infected and may
become
calcified if the infection is arrested
D. Progressive infection may produce ulcerative, hypertrophic ulcero-
hypertrophic
lesions
About 30% of patients show caecal lesions
disposed longitudinally
25
A. The immunity of the patient to the mycobacterium tuberculosis is low
include:
B. Leucocytosis
D. Pink colour
or tuberculous adnexitis
26
E. May cause blind loop syndrome
B. Paralytic ileus
C. Pelvic abscess
D. Shock
E. Internal fistulae
Typhoid perforation:
27
A. Circular in shape
B. Longitudinally directed
B. Diarrhoea
perforation include:
28
E. Four quadrant tap
E. Sickling test
is (are) essential:
A. Blood transfusion
B. Normal saline/Ringer’s lactate
29
C. Potassium
D. Magnesium
E. Digoxin
perforation include:
A. Ciprofloxacin
B. Tetracycline
C. Gentamicin
D. Penicillin
E. Metronidazole
A. New perforation
B. Entero-cutaneous fistula
C. Burst abdomen
D. Anaemia
E. Psychosis
A. Blood transfusion
B. Administration of pitressin
C. Administration of omeprazole
D. Resection of the terminal ileum
E. Sedation
30
A. Osteomyelitis
B. Cholelithiasis
C. Orchitis
D. Urinary tract infection
E. Myocarditis
Crohn’s disease:
Crohn’s disease:
In half the patients affects only the last 25cm of the terminal ileum
and
B. In a third of the patients the terminal ileum and the right colon are
affected
31
A. Oedema, hyperaemia and fine granularity of the serosa of the
affected segment
A. Fistula-in-ano
B. Pyrexia of unknown origin
C. Diarrhoea and vomiting
D. Generalized peritonitis
E. Entero-cutaneous fistula
A. Polyarthritis
B. Glaucoma
C. Entero-vesical fistula
D. Blind loop syndrome
E. Pericarditis
A. Sulphasalazine
B. Azothioprine
C. Steroids
D. Metronidazole
32
E. Interferon
A. Severe diarrhoea
B. Fistulae
C. Systemic manifestations
D. Downhill course of the patient
E. Persistent abdominal mass
A. It is better in children
Entero-colitis:
33
D. Causes subnormal temperature, tachycardia and circulatory failure
E. Has a high mortality: 50-100%
A. Chloramphenicol
B. Erythromycin
C. Oxytracycline
D. Amikacin
E. Ampicillin
Amoebiasis:
A. Absence of symptoms
B. Windy looseness of stools preceded by aching in the rectum
C. Nausea and vomiting
34
D. Abdominal colic, constipation, mucus and bright red blood in stools
E. Pyrexia, abdominal distension and tenderness
The ideal fluid to give to an ill patient with amoebic colitis and a
reasonable
renal output is:
A. Normal saline
B. Ringer’s lactate
C. Blood
D. Fluid 5:4:1
E. Darrow’s solution
35
E. Gel diffusion precipitation test
Amoebic perforation:
Amoeboma:
36
obstruction
D. Is best treated by operation
E. Must be differentiated from carcinoma, schistosomiasis and
tuberculosis
carcinoma is by:
37
A. Elongation of the colon
B. Oedematous dilated friable colon with numerous areas of necrosis
C. Discrete or confluent mucosal ulcers
D. Normal mucosa intervening the ulcers
E. Abscesses at the mesenteric border and peri-anal region
Severe diarrhoea, 30-40 motions a day, with mucus, pus and blood
in the
stools and associated fever and abdominal colic
B. Recurrent attacks of diarrhoea
C. Severe rectal bleeding
D. Intestinal obstruction
E. Peritonitis
A. Conjunctivitis
B. Spondylitis
C. Pyoderma gangrenosum
D. Psychosis
E. Portal hypertension
38
She is probably suffering from:
A. Disease restricted to the left side of the large bowel and rectum
B. Women
C. Patients developing their first attack in childhood or adolescence
D. Patients with at least 5 years history
E. Patients with the fulminating type
39
Disease exceeding 10 years duration
A. Exuberant granulations
B. Tubercles
C. Carcinomata
D. Papillomata
E. Ulceration
Lyphogranuloma venereum:
40
The primary ulcer in L.G.V.:
A. Is small
B. Is persistent
C. Is superficial
D. Is painful
E. Starts as a vesicle in the fourchette or anal margin in the female
Intestinal L.G.V.:
A. Is usually tubular
B. Has a constant lower limit at 3 to 5cm from the anal margin
C. May involve the anus, rectum, sigmoid colon and descending colon
D. Depends to a large extent on the duration of the antecedent procto-
colitis
41
E. Involves all the layers of the bowel wall but not the pararectal or
paracolic tissues
A. Vaginal stenosis
B. Perianal warts
C. Perianal granulomata and lymphorrhoids
D. Lymphoedema of the vulva
E. Bridges of skin across the labia
42
E. Stool microscopy for the causative organism
A. Sulphadiazine
B. Metronidazole
C. Oxytetracycline
D. Ampicillin
E. Amikacin
In diverticular disease:
43
A. The muscle is thickened
B. The mucosa is oedematous and ulcerated
C. The length of the bowel is shortened
D. There may be intramural or extramural abscesses
E. There is paucity of fat in the mesentery and bowel wall
A. Massive haemorrhage
B. Carcinoma
44
C. Localized pericolic abscess
D. Anal fistulae
E. Intestinal obstruction
A. Morphine, codeine
B. High fibre diet
C. Onions cabbage, peas, beans
D. Dioctyl sodium sulphosuccinate, normacol, isogel
E. Oxytetracycline,metronidazole, phthalylsulphathiazole
A. Diverticulosis
B. Massive haemorrhage
C. Fistula formation
D. An attack of diverticulitis
E. Abscesses
Entero-cutaneous fistula:
45
tissue
C. Has serious effects whether it is small or large intestine
D. If duodenal has a greenish discharge
E. If ileal or colonic gives a frankly faecal discharge
46
C. Haemoglobin, white cell count and differential
D. Serum bilirubin, alkaline phosphatase and plasma proteins
E. Plain chest X-ray
A. Colonic fistula
B. Continued profuse discharge
C. Wide cutaneous opening and intestinal mucosa continuous with skin
D. Fistula of hernial origin
E. Absence of obstruction distal to the fistula
Pilonidal sinus:
47
Fissure-in-ano:
Is a tear in the long axis of the squamous mucosa in the lower third
of
the anal canal
48
A. Purgation
B. Local application of a surface anaesthetic such as lignocaine in a
jelly base
C. Digital stretching of the anal sphincters under anaesthesia
D. Antibiotics
E. Codeine phosphate
Haemorrhoids:
A. Heredity
B. Sex
C. Manual work
D. Pregnancy
E. Chronic constipation
49
The symptoms of haemorrhoids include:
A. Pain on defaecation
B. Passage of bright red blood usually unmixed with faeces
C. Mucoid discharge and perianal discomfort
D. Chronic constipation
E. Recurrent diarrhoea
haemorrhoids include:
A. Haemoglobin
B. Sigmoidoscopy
C. Barium enema
D. Colonoscopy
50
E. Microscopy of faeces
A. Thrombosis
B. Neoplasia
C. Microcytic anaemia
D. Pruritus ani
E. Perianal suppuration
haemorrhoids include:
A. Purgation
B. High fibre diet or bran
C. Rectal ointments or suppositories
D. Sclerotherapy
E. Rubber band ligation
51
Post-operative complications after haemorrhoidectomy for
uncomplicated
A. Retention of urine
B. Pyeliphlebitis
C. Anal stenosis
D. Haemorrhage
E. Anal incontinence
A. Tubercle bacillus
B. Pneumococcus
C. Esch. coli
D. Bacteroides
E. Actinomycetes
Ano-rectal abscesses:
52
measure is:
A. Antibiotic therapy
B. Analgesia
C. Hot fomentation
D. Incision and drainage
E. Bed rest
A. Tuberculosis
B. Lymphogranuloma venereum
C. Amoebiasis
D. Actinomycosis
E. Carcinoma of the anus or rectum
53
Fistula-in-ano:
A. E.S.R.
B. X-ray of the chest
C. Barium enema
D. Sigmoidoscopy and proctoscopy
E. Swab of the pus for microscopy, culture and sensitivity of isolated
organisms
A. Perianal discharge
54
B. Ingestion of certain food items
C. No known cause
D. Parasitic infestation
E. Mycotic disease of the anal skin
A. Urinalysis
B. Microscopy of stools
C. Vaginal smear
D. Urethral smear in the male
E. Microscopic examination of perianal scrapings
measures include:
Washing of the anal region with warm water and soap after every
defaecation
and three times daily
B. Local application of steroids cream, or lotio mag. carbol or lotio
calamino
C. Phenobarbitone or diazepam three or four times daily
D. Mild laxatives
E. Analgesics
55
The commonest cause of acquired anal incontinence is:
A. Senility
B. Spinal tumour or injury
C. Tabes dorsalis and general paralysis of the insane
D. Trauma to the sphincters
E. Faecal impaction
In anal incontinence:
56
E. On palpation is found to consist of only two layers of mucosa
57
A. Intussusception
B. Irreducibility
C. Gangrene
D. Rupture
E. Ischaemic colitis
A. Lymphogranuloma venereum
B. Irritant enema and suppositories
C. Congenital anomalies of the anus
D. Impaction of foetal head in the pelvis
E. Post-haemorrhoidectomy
A. Diarrhoea
B. Attcks of flushing, bronchospasm and abdominal colic
C. Acute intestinal obstruction
D. Intestinal bleeding
E. Perforation
Melanin pigmentation of the lips, oral mucosa, face and hands and
58
recurrent
small bowel:
A. Leiomyoma
B. Neurofibroma
C. Adenoma
D. Intestinal polyposis
E. Fibrosarcoma
A. Hepatomegaly
B. Abdominal mass
C. Perforation
D. Macrocytic anaemia
E. Malabsorption syndrome
59
C. If in the appendix rarely metastasizes
D. Produces prostaglandins, kinins, histamine, indoles as well as 5HT
E. May cause pulmonary stenosis
Juvenile adenoma:
60
with adenomata
B. Is transmitted by females and the gene is dominant
C. Usually presents with lower abdominal pain and diarrhoea around
25 years
D. If untreated, becomes malignant about 25 years after the onset of
symptoms
E. Is treated by hemicolectomy of the more predominantly affected half
of the
large bowel
A. Desmoid tumours
B. Osteomata of the skull and mandible
C. Multiple lipomata
D. Multiple sebaceous and desmoids cysts
E. Familial polyposis
61
rectum and colon:
A. Stage B is when the growth has spread to the regional lymph nodes
B. The stage of a carcinoma depends on the duration of symptoms and
the
histological and biological characteristics and rate of growth of the
tumour
C. In the rectum 15% are stage A and B1, 35% stage B2 and 50%
stage C1, C2 and D
D. Stage A tumours contain the highest proportion of slow growing
tumours
E. Stage C tumours contain the highest proportion of cases of long
duration
of symptoms
A. Rectal bleeding – bright red blood mixed with faeces and mucus or
passed alone
B. Spurious diarrhoea
C. Haemorroids
D. Pain on defaecation
E. Enlarged inguinal lymph nodes
62
A. A lump
B. P.U.O.
C. Anaemia
D. Vague dyspepsia
E. Alternating constipation and diarrhoea
adopting alone:
63
B. Saline purges for 3 days before operation
C. Enema 2 days before operation
D. Rectal washouts night before operation
E. Oral mannitol 24hrs before operation
surgery include:
A. Nephrotoxicity
B. Agranulocytosis
C. Enterocolitis
D. Stomatitis
E. Fungal infection of the gut
64
C. Transverse colon is left hemicolectomy
D. Descending colon is left hemicolectomy
E. Sigmoid colon is sigmoid colectomy with or without left
hemicolectomy
Tumour more than 10cm from the anal verge is treated by anterior
resection
of the rectum
B. A tumour less than 10cm from the anal verge and poorly
differentiated is best
treated by abdomino-perineal resection of the rectum
C. A tumour between 5 and 10cm from the anal verge and either well-
or moderately
well-differentiated is best treated by low anterior resection
D. Adjuvant radiotherapy 4000-5000Gy reduces the incidence of local
recurrence
E. Pre-operative radiotherapy also improves the 5-year survival
65
A. Curative resection is possible in 50%
B. Palliative resection is possible in 20%
C. Patients with obstruction have an operative mortality of 25% and a
25%
5-year survival rate.
D. The crude survival of all patients at 5 years is 20%
E. The crude survival of all patients at 10 years is 14%
A. Prolapsed
B. Metabolic acidosis
C. Retraction and stenosis
D. Strangulation of small bowel
E. Dirrhoea
Adenocarcinoma
Fibrosarcoma
66
Basal cell carcinoma
Malignant melanoma
A. Common
B. Commoner in females
C. Always firmly attached to the coccyx and sacrum
D. Malignant when it presents after 2 months
E. Treated by excision, supplemented with radiotherapy and cytotoxic
therapy if
it is malignant
67
Concerning typhoid ileal perforation:
A. Has an incidence of up to about 20 percent of adult typhoid cases
B. Accounts for 40-50 percent deaths in typhoid fever
C. Is responsible for 20% cases of peritonitis excluding salpingitis
D. It occurs most frequently in the proximal ileum
E. Occurs more frequently in multiples
192. The necrosis in the Payer’s patches of the terminal ileum that
precedes ulceration
pathological processes:
68
Peritonitis from appendicitis
Amoebic colitis
Typhoid Perforation
Acute intestinal obstruction with strangulation
194. The most useful diagnostic investigation is:
195. The treatment regime of choice for patient in Question 193 is:
A. Immediate emergency surgical intervention
B. Conservative regime – expectant therapy, I/V, s antibiotics
C. Period of resuscitation and observation, intervening only if there is
no improvement
D. Resuscitation to get the patient fit for expeditions laparotomy
E. Resuscitation peritoneal paracentesis, with peritoneal lavage
196. In the resuscitation of the patient in Question 193 the most
important factor
determining the outcome of management is:
69
F. The pre-operative bicarbonate level
G. The pre-operative serum albumin level
H. The pre-operative serum sodium level
197. The three most commonly encountered complications following
the operative
treatment of the patient in Question 193 are:
70
melaena. On examination he is very pale, his pulse is 110/min,
BP 10O/60 and
the finger.
A. Upper GI Endoscopy
B. Urgent Colonoscopy
C. Stool microscopy
D. Blood culture
E. Stool culture
201. The treatment of choice for the patient in question 199 is:
A. Injection Sclerotherapy at Upper GI Endoscopy
B. Endoscopic rubber band ligation of varices
C. Urgent resuscitation and preparation for laparotomy
D. Resuscitation conservative management with exhibition of
Ciprofloxacin
and metronidazole
E. Resuscitation exhibition of Ciprofloxacin and metronidazole with
immediate
laparotomy
202. A twenty eight year old woman presents with a week’s history
71
of high fever,
headaches joint pains and pain in the right upper abdomen;
jaundice becomes
evident at the end of the week. Examination depicts a gravely
ill patient,
dehydrated jaundiced with tenderness and guarding in the
right upper quadrant
the abdomen; Murphy’s sign is positive.
203. How can the diagnosis of the patient in Question 202 be most
readily clinched?
A. Abdominal ultrasound
B. Plain x-ray of the abdomen
C. Blood culture
D. Urgent laparoscopic examination
E. Diagnostic abdominal tap
204. The treatment of choice in the patient in question 202 is:
A. Laparoscopic cholecystectomy
B. Laparotomy with view to open cholecystectomy
C. Resuscitation conservative management with exhibition of
ciprofloxacin/metronidazole.
D. Laparotomy with a view to exploration of the common bite duct.
E. Resuscitation and peritoneal lavage
205. The aetiological basis of Crohn’s Disease is yet to be
established. Which of
72
evidence?
73
207. The thickening of the bowel wall that characterizes Crohn’s
Disease is
maximally seen in the:
Mucosa
Muscolaris mucosae
Submucosa
The smooth muscle coat
E. Serosa
208. The distribution of Crohn’s Disease (Morphologically) is most
characteristically
in the:
74
211. A man of 35 visiting West Africa from Europe, complains of acute
onset of lower
abdominal pain, anorexia nausea, and vomiting accompanied by
diarrhoea of
two days duration. On examination he is dehydrated with low
grade pyrexia
(38.4°C) and there is tenderness with guarding localized to the
right iliac fossa.
75
of
zinc oxide ointments to the skin
C. (i) Daily stoma examination, (ii) exclusion of dietary element that
make it run (iii) regular dosing with buscopan
D. (i) Regular dosing with codeine phosphate (ii) daily stoma
examination
(iii) periodic zinc oxide application
E. (i) Daily soma examination (ii) periodic irrigation (iii) regular
dosing with buscopan
76
215. The diagnosis most commonly likely to be established is:
A. Examination of fresh stool specimen
B. Sigmoidocopy and Proctoscopy + biopsy
C. Mantoux test
D. Serological Tests including CFT (complement fixation test)
E. Microscopy and culture of vaginal fluids
216. The treatment of choice for the patient in question 214 is:
past two weeks she has noticed rectal pain and vaginal
discharge.
77
Ano-rectal tuberculous stricture
C. Stool culture
78
Increasing obesity, decreasing dietary fibre, increasing age,
decreasing
bowel content of spasmogens
Advancing age, increasing colonic pressures, increasing dietary
fibre,
decreasing transit time
79
Intermittent attacks
Ischaemic colitis
Irritable bowel syndrome
Diverticulitis
Paracolic abscess
Lymphogranuloma venereum
223. The diagnosis is most readily established by:
A. Sigmoidoscopy
B. Colonoscopy
C. Barium meal and follow through
D. Barium enema
E. Serological Tests including complement fixation test
80
CHAPTER 38
SMALL AND LARGE INTESTINES
ANSWERS
D 39. A, C, D, E 77. A. E
115. A, B, C
A, D, E 40. A, B, C, D 78. A, C, E
116. A, C, D, E
B, E 41. A, B, C 79. E
117. C
D 42. B, D, C 80. A, B, C
118. D, E
C, E 43. A, B, D 81. A, B, C, D
119. A, C
A, B, E 44. A, B, D 82. A, E
120. A, D, E
D 45. B, C, D, E 83. A, C, D
121. A, C, D
C, D 46. A, C 84. A, C
122. B, C, D
A, C, E 47. A, B, C 85. B, D, E
123. A, C, E
B 48. B, C, E 86. A, C
124. B, D
B, E 49. A, D, E 87. C, E
125. C, E
C, D 50. A, B, D 88. B
126. A, B, C, D, E
A, B, C 51. A, B, C, D, E 89. C
127. D
A, B, D, E 52. A, B, C, D, E 90. A, B, C
81
128. C, E
B, D, E 53. B, D 91. A, B, E
129. B, D
A, C, E 54. C 92. E
130. A, C
A, C 55. B, C 93. A, D
131. A, C, D
A, C 56. A, C 94. C
132. B, C, D
A, B, E 57. A, B, C, D 95. A, B, C, E
133. C, E
B, D, E 58. B, C, D 96. B, D
134. A, D
A, C, E 59. A, B, C, D, E 97. A, C, E
135. A, C, D, E
A, B, D, E 60. C, D, E 98. E
136. B, C
B, D, E 61. A, C, D, E 99. A, B, C, D
137. B, E
A, B, C, E 62. D 100. A, C
138. A, B, D, E
A, B, C, D 63. A, D 101. B, C, E
139. B, C
A, B, C 64. B, C, E 102. A, B, C, D, E
140. C, D
B 65. A, C 103. B, C
141. A, B
A, D, E 66. B, C, D, E 104. B, D
142. A, C, D
A, C, D 67. A, C, E 105. A, B, D, E
143. B, D, E
B, C, E 68. A 106. C
144. A, B, C
B, D 69. B, D 107. A, C, E
82
145. A, C, D
A, B, D 70. B, C 108. A, B, D, E
146
B, C 71. A, D 109. A, C, E
147. A, D, E
C 72. C, E 110. A
148. D
B, C, E 73. A, B, E 111. A, C, E
149.A, B, C, D, E
A, C, E 74. B, C 112. B, C, D
150. A, B, C
B, D, E 75. A, C, E 113. C, E
151. B, D
C 76. A, B, C, D, E 114. A, B
152. B, C, D
153. A, B, C, D, E
154. A, B, C, E
155. A, B, C
156. D
157. A, B, D
158. D
159. E
160. C
161. A, B, D
162. B, C, D
163. E
164. A
165. C, D
166. D
167. A, B, C
168. A, C, D, E
169. B, D, E
170. C, D, E
171. B, E
83
172. A, C
173. A, B, D, E
174. A, B, C, E
175. C, D
176. A, B, C, D
177. A, B, C
178. A, C, D
179. B, D
180. A, E
181. A
182. C, E
183. A, B, D, E
184. A, B, C, D, E
185. A, B, C, D, E
186. B
187. A, C, D
188. A, B, D, E
189. A
190. B
191. A, B, C
192. D
193. D
194. A
195. D
196. E
197. A
198. A, B, C, D, E
199. D
200. D
201. D
202. C
203. C
204. C
205. E
206. A
207. C
208. A
209. A
210. B
211. D
212. E
213. A
214. E
215. D
216. D
217. C
218. E
219. C
220. B
84
221. A
222. C
223. D
85
CHAPTER 40
PANCREAS
1. The most intimate posterior relation(s) of the neck of the pancreas is (are)
A. The aorta
B. The superior mesenteric vein and artery and portal vein
C. Splenic vein, the inferior vena cava and 2nd lumbar vertebra
D. The right crus of the diaphragm and the fibres of right psoas muscle
E. Splenic and inferior mesenteric veins
2. The “normal” pattern of the exocrine pancreatic ductal system – main
(Wirsung) duct joined by the minor (Santorini) duct which opens 2 cm
proximal to the main ductal entry into the duodenum-occurs in which percentage
of dissected bodies?
A. 80
B. 70
C. 60
D. 50
E. 40
3. Quantitatively and qualitatively the most important influence on pancreatic
exocrine secretion is the:
A. Intestinal phase
B. Vagal phase
C. Gastrin secretion
D. Cholecystokinin secretion
E. Output of 5 hydroxytryptamine
4. The following conditions follow exclusion of pancreatic juices from the
duodenum:
A. Profound gastric hypersecretion
B. Excessive losses of fat in the stool
C. Impaired absorption of vitamin B12
D. Nutritional hepatic damage
E. Chronic constipation
5. It is generally recognized that the diagnosis of pancreatic disease is
particularly difficult; which of these statements might account for this:
A. The organ is deep seated and completely retroperitoneal
B. It has a tremendous functional reserve even with 90-95% deficiency
C. It has a precarious blood supply
D. Close proximity to large vascular channels
E. Combination of exocrine and endocrine functions
F. Close proximity to the caeliac plexus.
6. In Pancreas Divisum:
A. The duct of Wirsung is diminutive, while the duct of Santorini assumes the major
channel of drainage
B. There is poorer drainage of t he organ through the minor papilla
C. There is high degree of association with recurrent pancreatitis
D. Recurrent abdominal pain is attributed to the anomaly
E. Levels of serum amylase and lipase are in the pathological range
7. In Ectopic pancreas:
A. The aberrant pancreatic tissue is in the stomach duodenum and jejunum
B. In 75% of cases the tissue is seen in the submucosa
C. In 75% of cases the lesions are symptomatic
D. Occurring in a Meckel’s diverticulum it produces the peptic ulcer syndrome
E. Sited in the small intestine, it may be the lead point of an intussusception
8. The following are considered regular pathological features of acute
pancreatitis:
A. Varying degrees of pancreatic ductal dilatation
B. Focal necrosis
C. Focal suppuration
D. Haemorrhagic areas
E. Gastric erosions
9. In normal individuals duodenal reflux into the pancreatic duct is
prevented by:
A. Oblique course of the pancreatic duct on its way to the duodenum
B. The tone of the duodenum
C. The activity of the sphincter of Oddi
D. Mucosal valves guarding the duct entrance
E. The valvulae coniventes of the mucosa
10. The principle(s) that activate(s) proteolytic enzymes in the pathogenesis
of most cases of acute pancreatitis is (are):
A. Increased serum activity of calcium ions
B. Infected bile
C. (Enteropeotidase)
D. Urogastrone
E. Phosphorylase A
11. The effect of activated pancreatic enzymes on the pancreas is the
production of:
A. Diffuse capillary, arteriolar and venous thrombosis
B. Diffuse small vessel haemorrhages
C. Interstitial oedema and acinar necrosis
D. Increased endothelial permeability
E. Capillary vasoconstriction
12. The effects of activated pancreatic enzymes on the pancreas include:
A. Increased tendency to platelet thrombus formation
B. Release of activated phosphorylase A attacking cellular membranes
C. Initiation of a reaction leading to release of kallidins and other
vasoactive amines
D. Increased cellular permeability
E. Necrosis
29. A man of 45 presents in the emergency room after a heavy meal with mild but
persistent, unrelenting epigastric pains radiating to the back, vomiting,
hicupping and constipation. The patient is fit, stout, anicteric and has persistent
epigastric tenderness with minimal guarding. There is no organomegaly and
patient has no past experience of dyspepsia.
The most likely diagnosis is:
A. Acute cholecystitis
B. Acute exarcerbation of duodenal ulcer
C. Slow leak of a peptic ulcer
D. Acute Pancreatitis (mild)
E. Early amoebic liver abscess
30. Which of these will most readily provide a lead to the diagnosis?
A. Full blood count
B. Abdominal ultrasound
C. Serum lipase estimation
D. Serum amylase estimation
E. Plain x-ray of the chest
31. A man of 40 presents with sudden onset of severe epigastric pains, repeated
vomiting, and persistent reteching. The attack, followed within half an hour of a
meal in which alcohol was not consumed. On examination his temperature is
39°C, pulse 96/min, BP110/70. He is tender in the epigastrium, with guarding and
rebound tenderness. The lung bases are dull to percussion and a pleural
effusion is detectable on the left side.
The most likely diagnosis is:
A. Perforated duodenal ulcer
B. Strangulating intestinal obstruction
C. Severe acute cholecystitis with gall bladder gangrene
D. Severe acute pancreatitis
E. Ruptured amoebic liver abscess
32. The diagnosis can most likely be confirmed by which of these investigations.
A. Upper GI endoscopy
B. Abdominal ultrasound
C. Abdominal CT scan
D. Estimation of serum C-reactive protein level
E. Serum calcium level
33. The treatment of choice in this patient is:
A. Preparation for early emergency laparotomy
B. Exhibition of bacteriocidal broad spectrum antibiotics
C. Resuscitation, antibiotic cover, nasogastric decompression
D. Resuscitation, antibiotic cover, bowel decompression, monitoring for need for
surgical intervention.
E. Resuscitation, bacteriocadal antibiotics, + trasylol
34. A 50 year old man, a known diabetic for 10 years, presents with severe unrelenting
abdominal pains of two days duration, vomiting, constipation. On examination he
is shocky, pulse 180/min BP 90/60, temperature 36°0°C. His abdomen is diffusely
tender with guarding and there is dark discoloration of the skin in the left flank.
The diagnosis is:
A. Dissecting aneurysm of the aorta
B. Intestinal obstruction with gangrenous bowel
C. Diabetic ketoocidosis
D. Fulminating acute pancreatitis
E. Severe acute cholecystitis with septic shock (SIRS)
35. The indicated treatment here is:
A. Resuscitation with IV fluids and implementation of the Alberti regime
B. Resuscitation with blood transfusion and antibiotics
C. Nasogastric decompression and monitoring for abdominal signs
D. Resuscitation, with IV fluids, bacteriocidal antibiotics preparation for bowel
resection
E. Resuscitation with IV fluids, bacteriocidal antibiotics, laparotomy for pancreatic
necrosectomy
36. In the confirmation of the diagnosis of acute pancreatitis urine estimations of
enzymes remain elevated for much longer; which is the most dependable urinary
test currently:
A. 24 hour total urinary amylase out put
B. 24 hour total urinary lipase out put
C. Urinary amylase excretion rate
D. Amylase/creatinine clearance ratio
E. Urinary amylase strip test (Rapignost-amylase)
37. The most useful diagnostic imaging procedure in acute pancreatitis is:
A. Plain x-rays of the abdomen
B. Ultrasonography
C. T99 Scentigram
D. CT Scan
E. Contrast Enhanced Computer Tomogram (CECT)
38. Which of these imaging techniques permits ready detection of pancreatic
necrosis?
A. Plain x-rays of the abdomen
B. Ultrasonography
C. T99 Scentigraphy
D. CT Scan
E. Contrast enhanced CT
39. By the leading systems of grading acute pancreatitis (Glasgow and APACHE II)
which of the following statements on proportions of mild pancreatitis is true:
A. 80-90% of cases follow a mild course
B. 70-80% of cases follow a mild course
C. 60-70% of cases follow a mild course
D. 50-60% of cases follow a mild course
E. 40-50% of cases follow a mild course
40. By the leading systems of grading acute pancreatitis (Glasgow and APACHE II)
which of the following statements in proportion of severe cases of pancreatitis is
true:
A. 10-20 % present as severe attack with mortality of 20-40%
B. 25-35% present as severe attack with mortality of 20-40%
C. 36-40% follow a severe attack with morality of 20-40%
D. 40-50% follow a severe attack with mortality of 20-40%
E. 50-60% follow a severe attack with mortality of 20-40%
41. By the Glasgow modification of the Ransom Criteria for Grading acute
Pancreatitis which of the following parameters reliably predict severe acute
pancreatitis:
A. Pa O2 < 60minHg
B. Serum urea > 16mmol/L
C. White cell count > 15 x 109/L
D. Glucose (FBS) > 10mmol/L
E. Calcium (serum) < 2mmol/L
F. Serum Albumin < 32 G/L
G. Serum AST (GOT) > 200U/L
H. Serum Lactic dehydragenase > 60U/L
53. A 45 year old alcoholic presents with severe epigastric pains, much retching and
vomiting of 48 hours duration. He is seen to be very pale with distending,
doughy, mildly tender abdomen with fluctuating signs. There is evidence of
shifting dullness and ultrasonography indicates presence of fluid in the
abdomen but the outlines of the liver, spleen and kidneys could not be
determined.
The most likely diagnosis is:
A. Bleeding Duodenal ulcer
B. Bleeding oesophageal varices
C. Acute Pancreatitis with rupture of rupture of an abscess
D. Acute Pancreatitis with spontaneous splenic rapture
E. Spontaneous haemoperitoneum from primary liver cell carcinoma
54. The prognosis in acute pancreatitis:
A. Has worsened in the past two decades
B. Is better with underlying gall bladder disease than with alcoholism
C. Is indifferent to the presence of met-haemoglobinaemia
D. Is much worse with operative intervention not-withstanding the preparation or
extent
E. Is not affected by mean levels of glucose attained in treatment
1
The enlargement allows inter position of bowel between the organ and
the abdominal wall
The enlarging spleen loses its contact with the splenic colic flexure
6. Accessory spleens:
A. Are found in at least 10% of subjects
B. Are more common in adult life
C. Undergo spontaneous atrophy in early childhood
D. Should be looked for and excised in all patients coming to splenectomy
for Trauma
E. Are most commonly found in the hilum of the spleen, region of the
pancreas, along the greater curvature of the stomach
F. Are most commonly found around the left testis
G. Often occur in the left broad ligament and pouch of Douglas
8. The following are readily extracted from the circulation by the spleen:
A. Leucocytes after a maximum age of 1 h
B. Platelets in general
C. Circulating lipoid elements
D. Erythrocytes of average age of 30 days
E. Plasma proteins
9. The main extramedullary site of haemopoiesis between the 5th and 8th
month of foetal life is:
The liver
The kidney
The spleen
Haemic nodes
Suprarenals
2
11. Which of these changes after splenectomy (is) are true:
A. Decrease in T and B lymphocytes
Stable but low serum 1g M levels
Temporary alteration in 1gG and 1g A
Decrease in opsonin activity
Decrease in complement levels esp. C3
Deficiency in phagocytosis
12. The risk of over whelming post splenectomy sepsis is highest in patients
requiring
splenectomy for:
A. Trauma
Thrombocytopenic purpura
C. Hereditary` spherocytosis
D. Thalassaemia
E. Non Hodgkin’s lymphoma
13. Two weeks after splenectomy for abdominal trauma a 38 year old man
returns
for follow up complaining of fever and painful swelling of the left leg of
3 days duration. Three days before this development he had noticed
headaches and joint pains and a dry cough.
The most likely diagnosis is:
A. Attack of malaria as post operative complication
Cellulitis of the left leg
Congestive cardiac failure
DVT
Thrombophlebitis of the left leg
3
C. Early fall in haemoglobin level
D. Increased resistance to malaria
E. Some impaired immunity to bacterial infection
16. The most useful index (hall mark) of splenic overactivity is:
A. Plasma bilirubin level
B. Plasma haptoglobin level
C. Reticulocyte count
D. Red blood count
E. Leucocyte count
17. The normal half-life (in days) of red cells as measured by the radio-
active
chromium plating technique is:
30
60
90
120
150
4
D. Thrombocytopenia, erythropenia, neutrophilia
E. Neutropenia, thrombocytopaenia, erythropaenia
24. The major criteria which establish the diagnosis of the tropical
splenomegaly syndrome include:
Spleen that is well below the costal margin
Spleen at least 2000G in weight
Residence in a malaria endemic area
Ig M level raised more than 25 times above normal
Good response to anti malarials
All the above
25. The minor criteria which establish the diagnosis of the tropical
spenomegaly syndrome include:
Liver biopsy showing hepatic sinusoidal lymphocytosis
Normal phyto haemoguttinin response
Evidence of hypersplenism
Lymphocyte proliferation
Familial occurrence
5
Multiple cyclical chemotherapy
Short courses of steroids
Segmental splenectomy
Splenectomy
32. A man of 40 has come to the surgical OPD with recurrent attacks of
abdominal discomfort, intermittent diarrhea with passage of mucus
6
and fresh blood over the past 4 years. On examination he was
apyrexial, not pale, but had signs of petichiae in the oral-mucosa and
bloctches on the skin. The abdomen was flat, non-tender, and there
were no masses. The liver, spleen and kidneys were not felt. P.R. –
the only finding was blood and mucus on the examining finger.
35. A Ghanaian woman of 35 who has suffered for many years with
seasonal (cold season) joint pains consults at the surgical out patients
complaining of epigastric pains radiating into the left hypochondrium,
fever and anorexia with vomiting of a week’s duration. On
examination she is icteric with mild anaemia, a pulse rate of 100/min
and BP 110/70; there is tenderness with guarding across the
eipgastrium, as well as a tender fixed mass in the left hypochondrium.
The Hb is 8.5G/dl, WBC 16,000/dl and a plain abdominal x-ray shows
a mass in the left hypochnodrium with a fluid level.
7
Resuscitation and exhibition of broad spectrum bacteriocidal
antibiotics
Percutaneous exploration of the mass under ultrasonic guidance
Open drainage of the localising abscess
Resuscitation splenectomy with drainage
Expectant management with mentoring of the mass
40. The mechanism for the genesis of portal hypertension is most often:
The result of increased portal inflow secondary to a hyperdynamic
systemic circulation
The result of increased portal inflow secondary to splanchnic
hyperaemia
Increased intra-hepatic post sinusoidal resistance within the portal
system
8
Increased extra-hepatic pre-sinusoidal resistance within the portal
system
Increased intra-hepatic pre-sinusoidal resistance within the portal
system
44. The treatment of choice for this patient (Question 42) is:
Endoscopic ligation/eradication of the varices by sclerotherapy
9
Bed rest and rest to the GI Tract
Protracted exhibition of propranolol
Tripple therapy
Conservative treatment using glypressin
46. The varices that bleed from the oesophagus in portal hypertension are:
Mucosal
Submucosal
Intermuscular
Intramucosal
Adventitial
50. The most useful investigative procedure for the diagnosis of bleeding
oesophageal varices is:
Barium swallow and meal
10
Splenic venography
Selective coelliac angiography
Oesophagogastroscopy
Radio-active scintigraphy
51. Needle liver biopsy may prove of value in the assessment of the patient
with portal hypertension to:
Exclude cirrhosis in alcoholics with apparent hepatomegaly
Distinguish intra-from extra-hepatic block
Identify hepatomegaly ostensibly produced by disease unlikely to cause
portal hypertension
Determine the state of liver function
53. In patients facing surgical intervention for liver disease the most
dependable measure of estimating the functional reserve of the liver is:
The Gardner Child scoring system
The Pugh-Child scoring system
Serum albumin level
Serum bilirubin level
Prothrombin level (seconds prolonged)
Presence of Ascites
Signs of Porto-systemic encephalopathy
Galactose Elimination capacity
Aminopyrine breath test
Hepatic Clearance of Aminoacids
55. Recent randomized controlled trials have shown that the most effective
agent for control of variceal bleed is:
I/V Infusin of Octreotide - 25-50µgm per hour for 48hr
11
I/V Terlipressin 2mg 6 hourly
Nadolol 60mg bd
I/V Glypressin + glyceryl trinitrite
Esomeperazole 40mg bd for 2/52
12
60. By current assessment, absolute contra-indications to shunt surgery in
portal hypertension include:
Established jaundice
Persistent ascites
Hypo-albuminaemia
Uncontrollable alcoholism
Hypo-gammaglobinaomia
61. The first line measures in the arrest of bleeding from oesophaeal
varices include:
Blood replacement, sedation with barbiturate, oral neomycin and
saline purge
Oral neomycin, volume replacement, and immediate endoscopy
Volume replacement, saline purge and use of the
SengstakenBlakemore tube
Sedation with morphine, oral neomycin and immediate endoscopy
Arrest of bleeding with the Sengstaken Blakemore tube and
barbiturate sedation
64. The indications for the deployment of the Sengstaken Blakemore tube
include:
Routine use in patients with proven bleeding varices
B. Patients with gastric varices
C. As a temporary holding measure in patients with uncontrollable variceal
haemorrhage
D. Routinely as a means of confirming diagnosis of haemorrhagic varices
E. In all patients who undergo injection sclerotherapy
65. The complications associated with use of the Sengstaken Blakemore
tube include:
A. Aspiration pneumonia
Pressure necrosis of the lower end of the oesophagus
13
C. Suffocation from displacement of the tube
D. Re-bleeding after deflation of the oesophageal balloon
E. Reflux oesohagitis
68. The simplest surgical intervention for patients with persistent bleeding
from oesophageal varices is:
Transgastric variceal ligation
Emergency transsection of the oesophagus
Gastric trans-section with para-oesophageal gastric devascularisation
Distal spleno renal shunt
Splenectomy
Splenectomy and spleno renal shunt
69. Which of these features (is)are true of the distal spleno-renal shunt
(Warren) used in the management of bleeding oesophageal varices:
Maintains a near normal portal blood flow
Does not decompress the viscera of the left upper abdomen
Provides complete freedom from Porto systemic encephalopathy
Has a lower rebleeding rate than porto-caval shunt
Maintains a lower portal pressure than the porto-caval shunt
14
Is the shunt of first choice for elective portal decompression
As the right upper abdomen is untouched leaves the option open for
later liver transplantation
73. The most urgent therapeutic needs of the patient actively bleeding
from oesophageal varices include:
Immediate oesophagogastroscopy
Transfusion of fresh blood, barbiturate sedation
Oral neomycin and saline purge
Early deployment of the Sengstaken Blakemore tube
Emergency portocaval shunt within 8 h of presentation
15
vasopressin:
Produces constriction of the splanchnic arterioles
Contracts the oesophageal musculature and this aids control
May be given in doses of 20 units 200 ml of saline over 20 minutes
In the effective dose may cause bowel evacuation and this may be
beneficial
May safely be exhibited in all individuals so afflicted
16
79. The prognosis in portal hypertension is dependent on:
A. Serum bilirubin levels above 2 mg/100ml
B. Serum albumin levels of less than 3g/100 ml
C. Prolonged prothrombin time over 2 seconds above normal
D. Presence of ascites
E. Elevated level of alkaline phosphatase
17
bleeding
B. The tension in the portal venous system is sustained
C. The varices are submucosal
D. Melaena is a more frequent presenting symptom than haematemesis
E. The bleeding is more frequently occult than obvious
18
A. Carries about 20% of the cardiac output
B. Is a branch of the celiac axis
C. Has a wary course following the upper border of the pancreas
D. Only occasionally gives rise to the short gastric arteries
E. May occasionally be aneurismal in female patients
93. In the patient with actively bleeding oesophageal varices the most
suitable first line
of arresting the haemorrhage after resuscitation is:
I/V Octreatide-therapy
Use of direct tamponade-Sengstake-Blakemore tube
Endoscopic banding
Endoscopic sclerotherapy
Trans-jugular, intra hepatic portosystemic stent shunt (TIPSS)
Transgastric ligation of the varices + splenectomy
Distal spleno-renal (Warren) shunt
19
CHAPTER 41
1. C 38. A 75. A, C, E
2. A, B, C 39. A 76. B, D, E
3. A, B, C, D 40. C 77. A, B, E
4. A, C, E, G, H 41. D 78. D
5. A, D, F 42. D 79. A, B, C, D,
6. A, E 43. C 80. A, B, C
7. A, B, C, D, E 44. A 81. A, B, C, D
8. B, C 45. A 82. D, E
9. C 46. B 83. A, C
20. A 57. C
21. B 58. A, B, C, D, E, F
20
22. E 59. B, C, D
23. D 60. A, B, C, D
24. A, B, C, D. E. F 61. A
25. A, B, C, D, E 62. B
26. A, B, C, D, E, F 63. C
27. E 64. C
28. C 65. A. B, C, E
29. E 66. D, E
30. D 67. A, B, C, D, E
31. E 68. A
32. E 69. A, F, G
33. E 70. D
34. C 71. A, B, C, E
35. D 72. A, C
36. D 73. B, C
37. A 74. A, B, C, D
21
CHAPTER 42
THE ADRENAL GLANDS
They cap the kidney at the level of the eleventh dorsal vertebra
peri-renal fat
The medulla is derived from mesoderm and the cortex from the
neural crest
Cortisol
17-ketosteroids
1
Oestrogens and progesterone
17-hydroxycorticosteroid
Testosterone
Nor-adrenaline
Angiotensinogen
Histamine
Aldosterone
Dopamine
A. Aldosterone
B. Cortisol
C. Adrenaline
D. Oestrogens
E. Androgens
6. Cortisol:
A. Increases glycogen deposition in the liver
B. Increases re-absorption of sodium and excretion of potassium by
cells
across cell membranes
C. Promotes gluconeogenesis
D. Inhibits peripheral utilization of glucose
E. Potentiates the action of insulin
7. Quantitatively, the most important steroid secreted by the
adrenal cortex is:
Testosterone
Cortisone
Aldosterone
Deoxycorticosterone
Cortisol
8. If in the ACTH Stimulation Test there is no rise in the urinary 17-
2
hydro-
xycorticosteroids and 17-oxosteroid from their initial value, the
most likely diagnosis is:
Hypopituitarism
Addison’s disease (primary adrenal insufficiency)
Cushing’s syndrome
Hyperplasia of the adrenal cortex
Carcinoma of the adrenals
9. If a patient is given 2 mg of dexamethazone in divided doses
daily and
the urinary 17-hydroxy-corticosteroid does not fall to less than 3
mg per
day by the second day, you will suspect:
A. Addison disease
B. Hypopituitarism
C. Cushing’s syndrome
D. Adreno-genital syndrome
E. Pituitary chromophobe adenoma
3
13. Clinical features of Addisonian crisis (acute adrenal insufficiency)
include:
A. Nor-adrenaline
B. Hydrocortisone
C. Fludrohydrocorisone
D. Aminoglutethimide
E. Metyrapone
15. Cushing’s Disease is caused by:
A. Adrenal adenoma
B. Adrenal carcinoma
C. Adrenal hyperplasia
D. Pituitary basophilic adenoma
E. Pituitary chromophobe adenoma
16. Cushing’s syndrome may be caused by:
Bronchogenic carcinoma
Treatment with exogenous cortisol
Carcinoma of the thymus
Hyperplasia of the adrenal cortices
Adrenal carcinoma
17. Cushing’s syndrome:
A. Is fairly common
B. Does not occur in infants or the elderly
C. Is 3-4 times commoner in women
D. May be associated with adrenogenital syndrome
E. Is most commonly caused by idiopathic hyperplasia of the
adrenal cortices
A. Increase in weight
B. Hypertension
4
C. Rounding of the face (“moon” face)
D. Easy bruising of the skin and multiple ecchymoses
E. Insulin-resistant diabetes
19. Causes of hypertension in Cushing’s syndrome include
Renal ischaemia
Premature arteriosclerosis
Excessive production of angiotensin
Retention of sodium
Retention of water
20. Causes of increase in weight in Cushing’s syndrome include:
5
C. Urine 17-hydroxycorticosteroid is markedly elevated
D. The urine free cortisol may be low
E. There is no response to cortisol suppression with small doses
of dexamethasone
A patient with a clinical diagnosis of Cushing’s syndrome has a
high
plasma cortisol level. On ACTH stimulation, there is no rise in the
plasma cortisol level:
A. Pituitary irradiation
B. Subtotal adrenalectomy
C. Bilateral adrenalectomy
D. Selective pituitary resection
E. External adrenal irradiation
28. Pre-operative measures in Cushing’s syndrome include:
6
Increased pigmentation
Premature baldness
Polymenorrhoea
Diminution in breast size
Atrophy of the clitoris and vagina
Deepening of the voice
34. Clinical features of the adrenogenital syndrome in girls at puberty
include:
Primary amenorrhoea
Enlargement of the clitoris
Acne
Atrophy of the muscles
Enlarged larynx
7
35. Clinical features of feminism include:
A. Increased libido
B. Rapid growth in prepubertal boys
C. Normal penis
D. Premature epiphysial maturation in prepubertal boys
E. Palpable adrenal tumour in about half of the patients
Urinary pregnanetriol
Plasma cortisol
Plasma testosterone
Urinary ketosteroids
Urinary cortisol
37. Congenital adrenal hyperplasia:
A. Nocturia
B. Headaches
C. Polydipsia
D. Anxiety and tremors
E. Tetany
40. In hyperaldosteronism:
8
A. The plasma rennin activity is high
B. The plasma aldosterone is elevated but the urinary
aldosterone is reduced
C. The urine has a high osmolality
D. The serum sodium is high
E. The Na/K ratio of the saliva is reduced
41. In primary hyperaldosteronism:
42. Phaeochromocytoma:
Excessive sweating
Paraesthesiae
Tremors and anxiety
Chest or abdominal pains
Weight loss and increased appetite
44. In phaeochromocytoma:
A. Bladder
B. Posterior mediastinum
C. Areas around the abdominal aorta
D. Spleen
E. In the liver
9
46. The most reliable diagnostic test in phaeochromocytoma is:
A. I.V.P
B. Blood samples taken at intervals along the inferior vena cava and
analysed for their CA content
C. CAT Scanning
D. Ultrasonography
E. Adrenal scintigraphy
Phentolamine
Propranolol
Proctolol
Phenoxybenzamine
Methyldopa
49. Dangerous hypotension following removal of phaeochromocytoma
is controlled with:
Nor-adrenaline
Blood
Large volumes of electrolyte solution
Methedrine
Propranolol
50. Possible causes of hypertension and hypokalaemia include:
A. Chronic pyelonephritis
B. Carbenoxolone
C. Liquorice
D. Oral contraceptives
10
E. Renal artery stenosis
A 40-year old man with headache, polydipsia and recurrent
attacks of weakness and paralysis of the limbs is found to have
a blood pressure of 180/110 mmHg:
53. Neuroblastoma:
Is a highly malignant tumour of the adrenal cortex and medulla
50% of cases occur before 2 years and 90% below 10 years
Spreads by the blood stream but not by the lymphatics
Has a knobbly contour
May secrete dopamine
54. Neuroblastoma:
Is usually painless
Often causes haematuria
May on straight X-ray of the abdomen show calcification
Is much more common in females
Is best treated by removal and irradiation of the area
55. In treating Addisonian crisis, one needs:
11
I.V. Normal saline
Potassium chloride
I.V. glucose
ACTH
Antibiotics
56. Adrenal incidentaloma:
CHAPTER 42
THE ADRENAL GLANDS
ANSWERS
A, C, D 32. E
C 33. A, C, E
12
A, C, D, E 34. A, B, C
A 35. B, D, E
B, D, E 36. D
A, C, D 37. A, C, D
E 38. B, E
B 39. A, B, C, E
C 40. D, E
D 41. B
A, D, E 42. C, E
B, C, D 43. A, B, C, D, E
A, B, C, D 44. B, C, E
B, C 45. A, B, C, D
D 46. D
A, B, C, D, E 47. C
C, D 48. A
A 49. B, C
D, E 50. B, C, D
A, C, E 51. E
B, C, D 52. A, B, C
A, D 53. B, D
B, C, D, E 54. A, C, E
A, C, E 55. A, C, E
B, C 56. B
A, C, D
13
A, C
B, E
A, C, D, E
A, B
A, B, C, D
14
CHAPTER 50
VASCULAR AND LYMPHATIC SYSTEMS
A. Thick
B. Relatively acellular
C. Non-wettable
D. Nourished via the vasa vasorum
E. Supplied by nerves
2. The media of an artery is:
Composed of fibro-elastic tissue and smooth muscle
Relatively thin but responsible for the strength of the arterial wall
In big arteries composed predominantly of muscle fibres
Nourished by the vasa vasorum
Separated from the adventitia by the internal elastic lamina
3. The veins:
Have the same capacity as the arteries
Have a wall consisting of muscle and fibro-elastic tissue
With the exception of the abdominal ones have valves which allow the
blood to flow only towards the heart
In the body cavities allow blood to flow as a result of the negative
pressure in the chest during respiration
Have sympathetic nerve supply
4. Where facilities exist, the investigations that MUST be done in every
patient
with peripheral arterial disease include:
1
Embolism
2
10. In atherosclerosis:
Lipids are deposited in the deeper layers of the intima
to form plaques
Plaques may become calcified or fibrosed
There is ulceration of the endothelium
The internal elastic lamina is thickened
The muscle of the media is replaced by fibrous tissue
3
Is probably an allergic reaction to nico-tine and regresses if smoking
is stopped
15. In thrombo-angiitis obliterans:
A. There is initial dense round cell infiltration of the adventitia
and media
B. There is endothelial proliferation of the intima
C. The lumen is occluded by a thrombhus which is later replaced by
firm granulation tissue
D. The lumen is never canalized
E. The artery or vein becomes enclosed in fibrous tissue
4
Patient is asleep
19. Signs of incipient gangrene of the foot include:
Coldness and numbness
Ulceration
Brittle nails and thin, shiny, hairless skin
Cyanosis of the toes
Absence of popliteal or dorsalis pedis pulse
A. The lower the level at which pallor of the sole appears when the leg is
elevated, the more severe the occlusion
B. Red discoloration of the sole when the leg is hanging suggests that
the ischaemia is not severe
C. A bruit at a particular site is due to dilatation of the artery above
the site of obstruction
Absence of the femoral pulse in both limbs is always indicative of
occlusion of the terminal aorta
Muscles of the affected limb are not wasted
21 In patients with chronic arterial occlusion of the lower limb:
About 40% improve spontaneously
About 55% remain unchanged
Only 5% require operation
Amputation is required in about 90% of those requiring operation
About half die within 5 years usually from C.V.A. or coronary
Thrombosis
22. In the medical management of chronic arterial occlusion of the
lower limb:
5
Smoking should be reduced
Fat intake should be low and the fat can be polysaturated
Leg exercises may increase the claudication distance by 8% and
improve
the physical and psychological state
Walking should be slow
23. Indications for operative treatment in chronic arterial occlusion of
the lower limb include:
Intermittent claudication
Rest pain
Inability to walk more than 150-200 m
Pregangrene
Absent popliteal pulse
A. Dacron
B. Autogenous artery
C. Autogenous saphenous vein
D. Glutaraldehyde stabilized umbilical vein
E. Nylon
25. Synthetic graft:
6
27. A cervical rib:
A. Right atrium
B. Infarcted myocardium
C. Aneurysm
D. Deep venous thrombosis
E. Subacute bacterial endocarditis
30. Common sites where a systemic embolus may lodge include:
7
A. Is swollen
B. Is infected
C. Is black
D. Has shriveled skin
E. Develops a red line of demarcation between the living and
dead tissue in a few days
33. In moist gangrene the affected part:
A. Is macerated
B. Always develops a red line of demarcation between the living and
and dead parts in a few days
C. Is green or black
D. Is not usually infected
E. Is not swollen
A. Aortic arch
B. Popliteal
C. Thoracic aorta
D. Femoral
E. Terminal abdominal aorta
37. Clinical features of an aneurysm include:
8
B. Marked pulsation
C. A thrill and systolic bruit over it
D. Reduction in the size and pulsation of the swelling when the artery
is compressed distal to the swelling
E. A smaller pulse distal to the swelling than on the contralateral side
38. In aneurysm of the abdominal aorta:
A. Hypertension
B. Peptic ulcer
C. Mitral incompetence
D. Hydronephrosis
E. Ischaemic heart disease
42. In the treatment of abdominal aortic aneurysm:
9
A. Excision of the aneurysm and replacement with a dacron graft is
preferred to an inlay tube graft
B. Aggressive fluid and electrolyte therapy including infusion of
mannitol is essential
C. Ischaemia of one or both limbs may occur post-operatively
D. The mortality in elective cases is only about 2%
E. About 50% of patients surviving operation are alive at 5 years
43. Renal artery stenosis:
10
superficial veins
B. Integrity of the osseo-fibrous compartment of the limb
C. Contraction of the veins
D. Contraction and power of the muscle bulk
E. Negative pressure in the abdominal cavity
47 The long saphenous vein:
11
Incompetent sapheno-femoral valve
51. Skin changes in varicose veins include:
53. A 40-year old woman has varicose veins of the right leg. When the
leg
is elevated with her in the recumbent position, the veins do not
collapse.
The cause of the varicosity may be:
Competent of the valves of the saphenous veins
Deep venous thrombosis
Incompetence of the sapheno-femoral valve
A pelvic tumour
Obstruction of the femoral or external iliac vein
54. If in the Brodie-Trendelenberg test, the varicose veins fill up from
below
immediately the patient stands up and before the tourniquet is
removed,
then the:
12
There must be obstruction in the deep veins
55. If in the Brodie-Trendelenberg test, the varicose veins do not fill up
when the
patient stands up from above when the tourniquet is released then
the:
58. The factors that maintain adequate venous circulation in the lower
limb
include:
13
Intra thoracic negative pressure maintenance
59. Varicose veins represent dilatation, elongation and tortuosity of
which
component of the lower limb venous system principally?
14
D. Uncomplicated (Early) varicose veins
E. Peripheral neuritis
F. Disc lesion – L4/5
G. Peripheral arterial embolism
62. How should this lady’s symptoms be best investigated:
15
65. A 40 year old diabetic man presents with recurrent itchy,
eczematous lesion
of his Rt. leg in the garter area, of nine months duration. He has
recently
experienced paraesthsia with recurrent breakdown of the skin. On
examination there is an ulcer just above the medial molleolus, with
shallow
sloping edges, firm, fibrotic base, depicting exuberant
granulations. There
are no varicose veins evident but there is a positive sapheno
femoral reflux
with a saphena varix.
16
69. Bleeding from a varicose vein is:
A. Pregnancy
B. Thrombo-phlebitis
C. Small varicose veins with competent valves of the communicating
perforators
D. Small varices following definitive surgery
E. Varicose veins with associated ulcer
72. The sclerosants currently in use for sclerotherapy of varicose vein
include:
A. Sodium morrhuate
B. Hydrocortisone in almond oil
C. Phenol in almond oil
D. Myodil
E. Sodium tetradecyl sulphate
73. The operative treatment of varicose veins:
17
as ulceration
C. Should in most cases be combined with Cockett’s operation
D. Has a mortality of about 1%
E. Has an average recurrence rate of less than 10%
74. What is the immediate treatment for the patient with varicose veins
complicated by acute bleeding from the region of the ankle?
18
78. The indications for operative management of varicose veins include:
Major varicosities
Incompetent perforators
First bleeding episode per se
Saphenofemoral incompetence per se
First episode of ulceration
Complication with superficial thrombophlebitis
Eczematous dermatitis
Ulcers – including grafting
Thrombophlebitis
Bleeding from varices
Chronic lymphoedema
80. The Cockets procedure (subfascial ligation of incompetent
perforators) is
indicated in all patients with:
A. Incompetent perforators
B. Recurrent varicose veins
C. Recurrent ankle ulceration and incompetent deep perforators at the
ankle
D. Incompetent perforators at the ankle
E. Varicose veins and chronic oedema
81. What instructions should be given to patients who undergo the
Trendelenberg operation for stripping of varicose veins.
19
veins
has been shown by recent Rendomised controlled Trials:
A. N. gonococcus
B. Wuchereria bancrofti
C. Chlamydia trachomatis
D. Haemophilus ducreyi
E. Herpes genitalis
85. Acute pre-or post-auricular lymphadenitis may be due to infection
of the:
20
86. External iliac adenitis or abscess:
A. Tuberculosis is the most likely cause if the age is under 10, and
and malignancy the most likely in those over 50
B. A short history is suggestive of acute infection and a long history
of chronic infection or malignancy
C. In the groin, pain is suggestive of acute inflammation, L.G.V. or
tuberculosis and absence of pain of malignancy or syphilis
D. Fever, malaise and myalgia are suggestive of acute or chronic
infection and not malignancy
E. Enlarged modes in the posterior triangle with a transient rash should
In endemic areas raise a suspicion of trypanosomiasis
88. In Lymphadenopathy:
21
maybe due to acute leukaemia
89. Investigations that will be useful in a 45-year old man with a 3-
month
history of enlarged lymph nodes in the right anterior triangle of the
neck
and a negative full clinical examination include:
A. V.D.R.L
B. Plain chest X-ray
C. Full blood count and E.S.R.
D. Blood film for microfilariae and aspiration of an enlarged node
E. Biopsy of an enlarged node
90. Lymphoedema:
A. Is accumulation of excessive amounts of interstitial fluid due to
inadequate
drainage as a result of obstruction of the lymph vessels
B. Affects the skin primarily
C. May also affect the muscles
D. Affects dependent parts of the body
E. Is primary if it is due to congenital mal-development of the lymph
vessels
91. Below-knee lymphoedema in a woman of 30 years in West Africa is
likely
to be due to:
22
A. Lymphoedema praecox
B. Trauma to the thigh
C. Tuberculosis of the inguinal nodes
D. Brugia Malayi
E. Metastases in the inguinal lymph nodes
93. Lymphoedema of the vulva alone in a 40-year old woman in West
Africa
is likely to be due to:
A. Lymphogranuloma venereum
B. Tuberculosis of the inguinal nodes
C. Chronic pyogenic sepsis of the vulva
D. Lymphoedema tarda
E. Wuchereria bancrofti
94. Lymphoedema of a breast in a 40-year old woman in West Africa
is likely to be due to:
A. Brugia malayi
B. Tuberculosis of the axillary lymph nodes
C. Lymphodema congenital
D. Axillary node metastases
E. Recurrent infection
Narrow and the lowest vertical nodes are not outlined while the
vessels
from the thigh and their corresponding nodes are normal, then the
cause is chronic sepsis
Dilated and tortuous and the nodes are not visualized, then
tuberculosis
Is the likely cause
23
Dilated and tortuous and the nodes are blocked or dilated, then the
likely
cause is filariasis
Not visualized, then aplasis is the most likely cause
Increased in number, caliber and tortuosity, then congenital varicose
dilation is the cause
97. Lymphoedema of the scrotum:
A. Is usually seen between 20 and 60
B. Is invariably accompanied by hydrocele
C. Does not usually involve the penis
D. May be associated with tiny vesicles of the skin of the scrotum
E. May be secondary to urinary fistulae
98. Unilateral lymphoedema of the lower limb in a 45 year old woman
should
be differentiated from:
24
best cosmetic result
B. Breast, amputation should be done
C. Vulva, antibiotics and diuretics suffice
D. Scrotum, excision should be done
E. Upper limb, amputation should be done
101. The histological types of Hodgkin’s lymphoma include:
A. Lymphocytic predomdinant
B. Nodular sclerosis
C. Histio-cytic predominant
D. Mixed cellularity
E. Lymphocyte depleted
102. Hodgkin’s disease:
A. Is pathologically characterized by the presence of giant cells
B. Is distributed throughout the world
C. Occurs in the third decade and over
D. Is “curable”
E. Is granulomatous rather than neoplastic
103. Hodgkin’s disease may present:
A. Most commonly as cervical or supraclavicular lymphadenopathy
B. As persistent pyrexia of unknown origin or cyclic fever
C. Often with paraplegia
D. With weight loss, lassitude or pruritus
E. With an abdominal “mass”
25
C. Lower extremity lymphangiogram
D. Lymph node biopsy
E. Staging laparotomy with splenectomy
106. In the Ann Arbor clinical staging of Hodgkin’s disease:
A. Stage I is limited disease of a single lymph node region or a single
extra-lymphatic organ or site
B. Stage II is involvement of 2 or more lymph node regions on the same
side of the diaphragm (II) or localized involvement of extra-lymphatic
organ or site and of one or more lymph node regions on both sides
of the diaphragm (IIE)
C. Stage III is involvement of lymph node regions on both sides of the
diaphragm (III) which may be accompanied by localized involvement
of the spleen (IIIS) or by solitary involvement of an extra-lymphatic
organ (IIIE) or both (IIISE)
D. Stage IV is diffuse or disseminated involvement of one or more
extra-lymphatic
organs or tissues with or without associated lymph node involvement
E. Lymphangiogram must be done in all cases
107. In the treatment of Hodgkin’s disease:
A. Stage I is treated by radiotherapy
B. Stages II is treated by radiotherapy and chemotherapy
C. Stages III and IV are treated by chemotherapy
D. The chemotherapy has been 6, 2-weekly cycles utilizing nitrogen
mustard,
vincristine, pro-carbazine and prednisone followed by a 2-week rest
period
E. Long-term disease-free remissions have been obtained in over 90%
of previously untreated patients
26
A. Block dissection is done for Stage I
B. Radiotherapy is used for Stage I disease
C. For Stages III and IV, the trend is to use radiotherapy and cyclical
chemotherapy
D. Currently, cyclophosphamide, vincristine and prednisone are given
every
21 days for 6 courses
E. Prognosis is best in the well-differentiated histiocytic lymphoma
110. Burkitt’s tumour:
A. Is the commonest malignant neoplasm in children in Africa
B. Does not occur outside of Africa
C. Occurs in epidemic form in parts of Africa
D. Has a high incidence across Africa within a belt 10-15˚ north and south
of the equator below 1500 m in altitude
E. Has the highest age incidence in both sexes between 4-12 years with
a
median age at 7-8
111. The histology of Burkitt’s lymphoma shows:
A. Lymphoctes-poorly differentiated
B. Undifferentiated lymphoreticular stem cells
C. Eosinophils
D. Histiocytes-well differentiated
E. Macrophages with abundant clear cystoplasm
112. Burkitt’s tumour presents most commonly as:
A. Cervical lymphadenopathy
B. Ascites
C. Painless progressive enlargement of one or more jaw quadrants
especially of the maxilla
D. An Abdominal mass
E. Flaccid paraplegia
27
C. Lungs, salivary glands
D. Subcutaneous tissues, long bones
E. Thyroid
115. Essential investigations in every confirmed case of Burkitt’s
lymphoma
include:
Liver biopsy
Intravenous pyelogram
Lumbar puncture for CSF cytology
Staging laparotomy and splenectomy
Bone marrow aspiration for cytology
116. Currently, the treatment of choice of Burkitt’s lymphoma without
CNS
involvement is:
A. Radiotherapy
B. Surgery for localized tumour
C. Cyclophosphamide administered as a single large dose of 40 mg/kg
I.V. and repeated for 4 courses at 2-3 weekly intervals
D. Methotrexate administered as a large dose I.V. followed by citrovorum
factor 24 h later
E. Cyclical combination chemotherapy with cyclohosphamide, vincristine
and methotrexate at 2-3 weekly intervals
117. It has been advised that following successful induction therapy in
Burkitt’s
lymphoma, there should be:
A. Blood transfusion
B. Monitoring of serum electrolytes and blood urea
C. Monitoring of blood uric acid
D. Administration of antibiotics
28
E. I.V. fluid therapy
119. In the prognosis of Burkitt’s lymphoma:
A. Long-term survival varies from 40-65%
B. About 50% of those showing remission have a relapse
C. Over 80% of those showing relapse have C.N.S. involvement
D. Chemotherapy has not been effective in relapse
E. Serum from cured patients has given favourable response in replapse
120. Sabfasical endoscopic perforator surgery has:
A. Proven a veritable minimally invasive alternative to open surgery
Lower recurrence rate to conventional open surgery
A higher neovascularization rate than conventional open surgery
A lower rate of failure to ligate long saphenous vein tributaries
A high success rate in locating and ligating significant perforators
121. Infective agents that have been implicated in the etiology of
lymphomas
include:
A. Helicobacter pylori
B. Human herpes virus-8
C. Hymenolepis nana
D. Hepatitis A
E. HTLV type I
122. The following are true of Hodgkin’s lymphoma:
123. In a patient with stage IIA Hodgkin’s Lymphoma you would expect:
29
D. Involvement of two or more lymph node regions on the same side
of the diaphragm
E. Unexplained fever
124. Gastric MALT lymphoma:
CHAPTER 50
VASCULAR AND LYMPHATIC SYSTEMS
ANSWERS
1. B, C 38. B, E 75. A, B, C, D, E
112. C, D, E
2. A 39. D 76. C
30
113. A, B
3. D, E, 40. E 77. B
114. A, B, D, E
4. A, C, D, E 41. A, B, D, E 78. A, B
115. B, C, E
5. C 42. B, C, E 79. A, B, C, D, E
116. C
6 A, D, E 43. B, C, E 80. C
117. E
7. C 44. C, D 81. C
118. A, B, C, E
8. A, B, D 45. C 82. A
119. A, B
9. C 46. B, D 83. A, E
120. C
10. A, C, E 47. A, D 84. A,B, C, D, E
121. A, B, E
11. A, B, C, D 48. C, E 85. A, D
122. B, D
12. B, C, E 49. A, B 86. A, B, C, E
123. B, D
13. A, C, E 50. E 87. B, E
124. A, B
14. C 51. A, B, C, D 88. A, C, E
125. A, C, E
15. A, B, C, E 52. A, C, D 89. B, C, E
16. A, B 53. B, D, E 90. A, D, E
31
CHAPTER 51
1
9
10
11
2
Which investigation will confirm the diagnosis?
Blood film
X-ray of the tibia
Hb electrophoresis
White cell count
Venogram
You will advise:
Ambulatory treatment with bandaging
Application of bland antiseptics and bed rest
Surgical debridement and grafting
Application of viscopaste to the leg
Dressing with Solcoseryl
A girl of 18 with Hb SC disease presented with acute
respiratory distress, cough and frothy sputum and soon after
admission became drowsy. On examination, the temperature
was 37˚C and there were petechial rashes on both arms; there
were no pulmonary signs.
3
Bronchoscopy
Pleural tap
Radioactive Xenon scan of the chest
Examination of the urine for fat globules
ECG
4
patient?
Osteochondritis dissecans
Subchondral and central sclerosis
Coxa vara
Flatening and irregularity of the femoral head
Milkman’s fracture
5
of 30
Is frequently marked by muscle tenderness
In its abdominal form may be indistinguishable from pancreatitis
Reticulocytosis ranging from 10-15% may be associated with it
In sickle cell disease:
Not all patients are found to be anaemic
Symptoms only begin to manifest after 3 months of life
The average (steady state) Hb level for SC patients is 8g/dl
The most severe anaemia occurs with SB thalassaemia
Growth disturbance may produce a stunted figure, much below
average weight
6
An attack of falciparum malaria
Typhoid fever
Sequestration syndrome of sickle cell disease
Splenic infarct
Viral hepatitis A
The most useful diagnostic investigation is:
Plain x-ray of the chest-erect
Plain x-ray of the abdomen-erect
Abdominal ultrasound
Liver function tests
A full haematological profile
7
The most likely diagnosis is:
Recurrent attacks of malaria
Recurrent attacks of typhoid
Osteomylitis of the left tibia
Hand foot syndrome of sickle cell disease
Attacks of Dengue fever
The most useful diagnostic test is:
Blood film for malarial parasites
Blood culture
A full haematological profile
Chest x-rays
Liver function tests
8
patients blood count is reported as “Total WBC 40,000/cub
mm, including normoblasts with reticulocystosis – 12%.
9
11gm/dl
12gm/dl
The average steady state Hb maintained by patients with Sickle
Cell disease (Genotype SC) in the typical socio-economic
circumstances in West Africa is:
8-9gm/dl
10-11gm/dl
12-13gm/dl
14-15gm/dl
16gm/dl
10
Haemolytic jaundice attendant on repeated episodic sickle cell
crises
Hepatocellular Jaundice – Hepatitis A
Hepatocellular jaundice – Hepatitis B
The test most likely to clinch the diagnosis is:
Percutaneous Transhepatic Cholangiography (PTC)
Endoscopic retrograde Cholangiopancreatogrophy (ERCP)
Magnetic Resonance Cholangiopancreatogrophy (MRCP)
Hepatic Scintigraphy
Helical CT Scan of the abdomen
The treatment for the patient in Question 32 is:
Resuscitation + adequate nutritional supplements
Resuscitation + check on G6PD status and review of charted
drugs given
Bed rest and attention to urgent nutrition needs
D. Resuscitation + monitoring for signs of progression and need for
surgical
intervention
E. Resuscitation, I/V administration of 10% fructose, Vitamin. K and
prophylactic antibiotics
11
splenism in a patient with splenomegaly in Sickle Cell Disease,
and therefore requiring splenectomy?
The spleen is > 4cm below the Lt. costal margin
The HB falls < 6.5g/dl
The reticulocyte count exceeds 15%
The platelet count falls below 200 x 109/l
None of the above
A man of 25 presents in the Emergency Room with a sudden
onset of severe pain in the left hypochondrium, much
worsened on inspiration. He is a pyrexial, and anicteric; his
chest is clear and has a tender mass that moves with
respiration in the left hypochondrium. There have been no
previous attacks:
12
May be due to viral hepatitis
Is attended by the morbid anatomical change of sinusoidal
engorgement with fibrin clots
Is marked by central lobular parenchymal necrosis
Is very frequently attended by jaundice of obstructive
intrahepatic type
May be accompanied by fever, leucocytosis and abdominal pain
Hepatomegaly in sickle cell disease:
Is frequently associated with extrahepatic ductal obstruction by a
stone
Is attended by sinusoidal haemosiderosis
May be associated with biliary canalicular thrombi
May on occasion be an indication for laparotomy
Is often seen with anasarca
Jaundice in sickle cell disease:
Is most frequently acholuric arising from excessive red cell
destruction
May produce an elevation of both direct and indirect reacting
bilirubin
May be difficult to distinguish from extrahepatic ductal
obstruction
May on occasion be an indication for laparotomy
Should initially be treated conservatively with adequate fluids
and nutritional supplements
13
Is characteristically reduced to a small nubbin of fibrous tissue in
adolescent SS patients
Is seldom reduced in size in patients with SC disease
May occasionally require removal as a measure to reduce
frequency of haemolytic episodes
The kidney in sickle cell disease:
May show defective tubular concentration in the form of
hyposthenuria
Has a tendency to excessive concentration of urine
Is often grossly enlarged (symmetrically)
Need not be investigated for other causes of haematuria in
patients presenting with haematuria
If the source of unilateral presistent bleeding may require
surgical excision
Haematuria in sickle cell disease patients:
Occurs in 2-4% of Hb SS and Hb SC patients
Is more likely to arise from causes other than the sickling lesion
in the kidney
May be prolonged and recurrent and usually painless
Is treated with blood transfusion, alkaline infusions and
occasionally aminocaproic acid
May warrant a nephrectomy if unilateral and persistent
14
Arises usually from ulcerations of the renal papillae, the result of
papillary infarct
Is likely to be persistent because of constant contact of the
ulcerating lesion with urokinase
Is usually total and recurrent
May be treated by blood transfusions, alkaline infusions and
diuretics
Is never life threatening enough to warrant nephrectomy
The recurrent haematuria which occurs in some 2-4% of patient
with Sickle Cell disease (Hb SS and SC) arises from:
Ulceration of the tips of the renal papillae
Infarction in the medulla of the kidney
Sickling phenomena in the cortex of the kidney
Ulceration in the trigone of the bladder
Infacts of the mucosa of the renal pelvis
The bleeding in Sickle Cell haematuria becomes repetitive and
persistent because:
Of repeated episodes of sickling crisis
The hyposthenuria that accompanies Sickle Cell disease
Febrinolytic enzymes (urokinase) being continuously in contact
with
the urine
High pH of the urine in Sickle Cell disease
Attendant urinary tract infection
The first line management in Sickle Cell patients with
haematuria is:
Intravenous infusion of alkalinizing agents (NaHCO3)
Blood transfusions
Administration of diuretic agents
Infusions of Amino caproic acid
15
Infusion of ringers lactate
16
Should be treated by bed rest and wound dressing with mild
antiseptics
17
B. Is more often than not associated with varicose veins with
incompetent
perforatiors
Is usually deep seated with exposure of muscle, tendon and
periosterum
Shows no stratification of incidence in socio economic groups
Is frequently complicated by malignant degeneration
18
A. Is seldom a cause for a crisis
B. Occurs as frequently as in the general population
C. Characteristically affects the lower lobes
D. Is common because of pulmonary congestion, thromboses and
impairment of immunity on account of autosplenectomy
E. Is often complicated by cardiac arrhythmias and right heart failure
19
capillaries of periphery of fundus
C. Retinal, choroidal and anterior uveal infarcts
D. Micro-aneurysms, dilated capillaries and veins
E. Proliferative neovascularization of the vitreous from which vitreous
haemorrhages may occur
62. Ocular changes in sickle cell disease may take the form of:
A. Heightened flow in the arterioles of the fundus with silver wiring
appearance
B. Ischaemic areas showing whitening of the retina
C. Haemorrhages of varying severity which may be retinal, peri-
retinal
D. Neovascularization of the retina, budding capillaries, a
compensatory
reaction to retinal ischaemia
E. Tears and detachment of the retina
20
64. In the management of patients with sickle cell disease:
A. Blood transfusion is more useful than alkaline infusions in
decreasing
the sickling tendency
B. Oxygen therapy has no immediate effect on the sickling process
C. Prophylactic antimalarial therapy is of proven benefit
D. Prophylactic Vit. B12 has been found beneficial
E. Efforts should be made to achieve pre-operative Hb levels of 12
g/dl
in adults
65. In the management of patients with sickle cell disease:
A. Expanding the plasma volume using alkaline and dextrose
infusions
decreases the sickling tendency
B. Oxygen therapy relieves the pain and other distressing
symptoms
accompanying crises
C. Search for and prompt treatment of acute infections may abort a
crisis
D. Anticoagulants such as Arvin may prove useful in aborting or
arresting
an attack
E. Efforts should be made to achieve pre-operative Hb levels of 10
g/dl
in children
21
D. Take the form of the classic cod-fish appearance
E. May take the form of collapse of the vertebral bodies
67. The pathological changes of sickle cell disease affecting the
hip:
A. Are common and indistinguishable from Perthes’ disease
B. Are more common in Hb SS patients than SC or other varieties
C. Are usually related to some sepsis in the upper end of the
femur
or hip joint
D. May produce septic dislocation of the hip
E. May result in total sequestration of the femoral head
68. The pathological changes of sickle cell disease affecting the
hip:
A. Are rare and distinct from all childhood hip affections
B. Usually results in bony ankylosis
C. Are nearly always the result of early experience of trauma to the
hip
D. Are frequently arrested by prolonged bed rest with the affected
limb
in traction
E. Are seldom bilateral
69. The head of the humerus in sicklers:
A. Is notably subject to infarction though not as frequently as the
femur
B. Does not deform as badly as the femoral head
C. Is more liable to develop early osteoarthritis than in the normal
population
D. Usually escapes early osteoarthritis
E. Showing avascular necrosis is best treated by short wave
diathermy
and mobilization exercises
70. Osteomyelitis in sickle cell disease:
22
A. Affects nearly 90% of Hb SS patient in one or more bones
before
the age of 10
B. May start anywhere along the shaft of the long bone
C. Usually starts in the metaphysis and spreads down the
diaphysis
D. Has a less stormy course than in the Hb AA patient
E. Should be treated by parenteral ampicillin and cloxacillin
71. Osteomyelitis in sickle cell disease:
A. Affects nearly 50% of Hb SS patients in one or more bones
before
the age of 10
B. Not uncommonly produces segmental lesions along the shaft
of the same bone
C. Is most frequently produced by staph. pyogenes
D Is frequently complicated by septicaemia
E. Should be treated by oxygen therapy, antibiotics, limb
immobilization
and timely evacuation of intramedullary pus
72. For children with Sickle Cell disease the principal cause of
post
operative morbidity and mortality is:
A. Acute chest syndrome and splenic sequestration
B. Post operative malaria
C. Dehydration
D. Urinary tract infection
E. Low Hb in the post operative period Hb < 8.0g/dl
73. In patients with Sickle Cell disease undergoing operation it
is generally
recommended that to obtain the normal P02 tension in the
system the
oxygen ventilation during surgery should be at least:
23
A. 20%
B. 25%
C. 30%
D. 35%
E. 40%
CHAPTER 51
ANSWERS
1. A 38. C
2. A, B, C, D, E 39. A, B, C, E
3. D 40. B, C, D
4. B 41. A, B, C, D, E
5. A 42. A, B, C, D, E
6. A 43. A, C, E
7. D 44. A, B, C, D, E
8. C 45. A, B, C, D
9. C 46. A
10. D 47. C
11. D 48. A
12. D 49. A, B, C, D, E
13. A, B, C, D 50. D, E
14. A, B, C, D 51. D
15. A, B, C, D 52. A, B, C, D, E
16. B 53. A, D, E
17. A, B, C, D, E 54. A, B, C, D, E, F
18. B, C, D, E 55. A
19. A, B, (D) E 56. A
24
20. C, D, E 57. C
21. C 58. A, B, C, E
22. E 59. C, D, E
23. C 60. A, B, C, D, E
24. D 61. A, B, C, D, E,
25. C 62. B, C, D, E
26. D 63. B
27. E 64. C
28. A 65. A. B, C, E
29. D 66. A, B, C, D, E
30. A 67. A, C, D, E
31. B 68. D
32. C 69. A, B, C, E
33. C 70. A, B, E
34. D 71. B, C
35. D 72. A
36. A, B, C, D 73. C
37. C
25
CHAPTER 26
THE HEART
1
D. An antecubital vein
E. A radial artery
2
13. Atrial septal defect:
A. Represents a right to left shunt
B. May close spontaneously
C. Is asymptomatic in the majority of infants and children
D. Shortens life expectancy although survival to adulthood is the rule
E. Is characterized by a soft mid-systolic murmur at the pulmonary area
and
physiological splitting of the second heart sound.
14. Ventricular septal defect:
A. Most commonly occurs in the perimembranous area
B. The conduction tissue is closely related to its margin
C. May close spontaneously
D. Causes a right to left shunt
E. Increases pulmonary blood flow
15. Ventricular septal defect:
A. Closes spontaneously in about 90% of patients usually by 6 months of
age
B. Causes a pansystolic murmur
C. If large, may lead to hypertensive pulmonary vascular disease
D. Is often complicated recurrent pulmonary infections
E. Eisenmenger’s syndrome is an indication for urgent surgical closure
16. Features of ventricular septal defect include:
A. Bi-ventricular enlargement
B. A thrill in the 3rd or 4th right intercostal space
C. A loud holodiastolic murmur in the lower left sternal border
D. Oligemic lung fields on P-A chest films
E. Boot-shaped heart on P-A chest films
17. Contra-indications to surgery in ventricular septal defect include:
A. Age less than 10 years
B. Reversible pulmonary hypertension
C. Zero net shunt across the defect
D. A large defect with retarded growth and recurrent pulmonary infections
E. Eisenmenger’s syndrome
18. Congenital pulmonary valve stenosis
A. Is preferably treated by surgery in the current era
B. Causes reverse splitting of the second heart sound
3
C. Is preferably treated by catheter intervention techniques currently
D. May coexist with annular and infundibular hypoplasia
E. Commonly presents in adulthood.
4
24. In congenital aortic stenosis:
A. Left ventricular ejection time is prolonged
B. Diastolic time is prolonged
C. Coronary arterial filling time is prolonged
D. Neonatal intervention may be required
E. Myocardial ischemia is often evoked
25. Notching on the posterior aspects of the 3rd to 8th ribs on both
sides in a 10-
year old boy is typical of:
A. Congenital aortic stenosis
B. Congenital pulmonary stenosis
C. Arterial hypertension
D. Patent ductus arteriosus
E. Coarctation of the aorta
26. Complications after correction of congenital aortic stenosis include:
A. Residual obstruction
B. Re-stenosis
C. Aortic incompetence
D. Mitral incompetence
E. All of the above
27. Coarctation of the aorta:
A. Is a localized deformity of the aortic adventitia
B. Is more commonly juxta-ductal
C. Ductal closure is contributory to the etiopathogenesis
D. Occurs in the region of the aortic isthmus
E. The left subclavian artery may be used for patch aortoplasty
28. Coarctation of the aorta:
A. Causes a significant pressure gradient in the aortic isthmus
B. May be in the thoracic or abdominal aorta
C. May be associated with aneurysm of the aorta
D. Collaterals cause rib notching
E. Is commonly associated with bicuspid aortic valves and intracranial
aneurysms
29. Symptoms of coarctation of the aorta include:
A. Headaches
B. Epistaxis
C. Upper extremity hypertension
5
D. Abdominal pain after meals
E. Feeble lower limb pulses
30. Useful investigations in suspected coarctation of the aorta include:
A. Cardiac catheterization
B. Aortography
C. E.C.G.
D. Plain chest X-ray
E. Echocardiography
6
D. A systolic murmur is heard in the neck
E. The second heart sound is normal
36. The most essential investigation in suspected Tetralogy of Fallot is:
A. Plain chest X-ray
B. E.C.G.
C. Echocardiography
D. Cardiac catheterization and angiocardiography
E. Blood gas studies
7
include:
A. Balloon atrial septostomy
B. Anastomosis between the right pulmonary artery and the ascending
aorta
(Waterston shunt)
C. Atrial septectomy (Blalock-Hanlon operation)
D. Interventricular septectomy
E. Atrial switch operation (Mustard procedure)
8
commissures
D. Is a funnel-shaped orifice which becomes narrower but less deformed
with time
E. Becomes clinically significant about 10 months after the acute valvulitis
46. In acquired mitral stenosis:
A. Symptoms start when the cross-sectional area of the valve is less than
2.5 cm2
B. The left atrium and the right ventricle enlarge
C. There may be functional tricuspid stenosis
D. Paradoxical peripheral embolization may occur
E. Pulmonary hypertension occurs
47. In mitral stenosis the symptoms include:
A. Paroxysmal nocturnal dyspnoea
B. Orthopnoea
C. Dyspnoea on exertion
D. Cough
E. Easy fatiguability
9
B. Consequent dilatation of the left ventricle worsens the regurgitation
C. Left ventricular function deteriorates with time
D. The pulmonary vascular resistance falls
E. Chronicity tends to induce intractable atrial fibrillation
52. The initial symptoms in rheumatic mitral insufficiency include: []
A. Easy fatigue
B. Orthopnoea
C. Exertional dyspnoea and palpitations
D. Cough
E. Paroxysmal nocturnal dysponea
53. Signs of rheumatic mitral insufficiency include:
A. Pansystolic murmur most prominently heard at the bases and radiating
to the left axilla
B. A diastolic flow murmur with an opening snap at the apex
C. A loud first heart sound
D. A prominent apical thrust of the heart which may be displaced
downwards and
laterally
E. Machinery murmur
10
lactation.
57. The clinical examination reveals features of rheumatic aortic
regurgitation in a
55 year-old man. You would recommend aortic valve replacement
under the
following conditions
A. NYHA Class III or IV symptoms
B. Asymptomatic with ejection fraction at rest of 40%.
C. Asymptomatic with ejection fraction at rest of 65%
D. Intractable symptoms despite adequate medical therapy.
E. The diagnosis alone is sufficient indication for surgery.
58. The following is/are true of arterial blood gases (ABG):
A. ABG reflects lung function.
B. Venous blood gases reflect the adequacy of tissue oxygenation and
tissue carbon dioxide clearance.
C. In a hypoxaemic patient, air contamination of the ABG sample
produces an underestimation of the patients arterial PO2.
D. ABG samples need not be iced if the sample is analyzed within 10
minutes.
E. The metabolic effects on the ABG sample are caused primarily by the
activity of erythrocytes.
11
C. Recurrent pharyngeal nerve palsy.
D. Phrenic nerve injury with diaphragmatic paralysis.
E. Re-coarctation.
61. Death in untreated aortic coarctation is usually due to:
A. Heart failure.
B. Aortic dissection.
C. Infective endocarditis.
D. Cerebral hemorrhage.
E. All of the above.
62. In Eisenmenger’s syndrome
A. Pregnancy is contraindicated in female patients.
B. During pregnancy, maternal and foetal mortality are similar,
approaching 50%.
C. Flying on commercial airline flights can be safely performed by stable
patients with SPO2 on room air of 85%.
D. Right-sided heart failure and supraventricular arrhythmias are
harbingers of poor prognosis.
E. Intravenous lines carry an increased risk of morbidity or mortality.
63. A "clinically significant" ASD:
A. Causes right heart volume and sometimes pressure overload.
B. May be associated with atrial arrhythmias in those older than 30 years.
C. May permit paradoxical embolism resulting in TIA/stroke.
D. May lead to paroxysmal nocturnal dyspnea.
E. Has a pulmonary-to-systemic flow ratio of 1.
12
65. Indications for surgery in mitral regurgitation include:
A. Absence of symptoms
B. Minimal to moderate symptoms
C. Atrial fibrillation
D. Progressive symptoms with left ventricular decompensation
E. Severe left ventricular enlargement and failure
66. Acquired aortic stenosis:
A. Is more common in males and syphilis is probably the commonest
cause
B. Becomes symptomatic when the normal cross-sectional area of the
valve is reduced to 1.0cm2
C. Leads to increase in coronary blood flow to cope with the LV
hypertrophy
D. Has no effect on the right heart or pulmonary vessels
E. Produces early symptoms in most patients
67. Early features of acquired aortic stenosis include:
A. Sudden death
B. Pulmonary oedema
C. Exertional syncope, dizziness or dyspnoea
D. Left ventricular failure
E. Angina pectoris
68. Signs of acquired aortic stenosis include:
A. Arterial hypertension
B. Diastolic thrill in the aortic area
C. Crescendo-decrescendo murmur in the 2nd intercostal space along the
right sternal border
D. Radiation of murmur to the suprasternal notch and the carotids
E. Slow-rising pulse
13
E. Dyspnoea of any degree
70. Aortic regurgitation:
A. May result from type A aortic dissection
B. May remain asymptomatic for many years
C. May initially give rise to throbbing in the head and neck
D. Gives a wide pulse pressure due to the very high systolic pressure
E. Is characterized by a blowing aortic systolic murmur
71. A 45-year old man suffering from fatigue and dyspnoea for 3 months
is found
to have distended neck veins which increase on inspiration, pulsus
paradoxus, hepatomegaly, and ascites out of proportion to pedal
swelling.
14
A. Congenital aortic stenosis
B. Atrial septal defect
C. Ventricular septal defect
D. Tetralogy of Fallot
E. Patent ductus arteriosus
75. Recurrent Stokes-Adams attack may be associated with:
A. Severe bradycardia
B. Exertional dyspnoea and dizziness
C. Syncope
D. Angina pectoris
E. Convulsions
76. Heart block may be caused by:
A. Coronary artery disease
B. Aortic valve replacement
C. Perimembranous VSD closure in children
D. Digoxin toxicity
E. Conduction system degenerative disease
77. In complete heart block:
A. The stroke volume is increased
B. Physical activity is accompanied by tachycardia
C. The heart rate is 45 or less
D. The E.C.G. shows infrequent QRS waves associated with P waves
E. Atropine is often used for symptomatic relief
78. Concerning myocardial hypertrophy:
A. The pattern of hypertrophy reflects the nature of the stimulus.
B. Pressure-overloaded ventricles develop concentric hypertrophy
C. Volume-overloaded ventricles develop hypertrophy with chamber
dilation
D. Pressure-overload hypertrophy is accomplished predominantly by
augmentation of cell width via parallel addition of sarcomeres
E. Volume overload and/or dilation stimulate augmentation of both cell
width and length via both parallel and series addition of sarcomeres
15
A. Atheroma
B. Fibromuscular dysplasia
C. Dissection
D. Spasm
E. Embolism
80. The physiology of the coronary circulation can be described thus:
A. In the absence of significant pathology, coronary arterial flow provides
adequate myocardial perfusion at rest
B. Compensatory vasodilation provides flow reserve that is more than
sufficient to accommodate the increased metabolic demands during
vigorous exertion.
C. When the luminal cross-sectional area is decreased by 50% or more,
coronary blood flow generally becomes limited with exertion
D. With 60% or greater reduction, coronary flow may be inadequate even
at rest
E. Coronary artherosclerosis is not the commonest cause of coronary
obstruction
81. The following are true concerning bicuspid aortic valves (BAV):
A. BAV is the most frequent congenital cardiovascular malformation in
humans.
B. Men are affected three to four times more frequently than are women.
C. BAV are predisposed to accelerated calcification, with about 85%
becoming stenotic
D. About 15% of the time, they become purely incompetent, complicated
by infective endocarditis, or associated with acute aortic dissection.
E. BAV underlie over two-thirds of aortic stenosis in children and 50% of
adults
82. The pulse generator of an artificial pacing system:
A. Can be programmed to fire at a fixed rate completely uninfluenced by
the heart
B. Can be programmed to function only during periods of complete heart
block
C. May be complicated by loss of capture, infection or lead migration
D. Has a life span of 30-40 years when implanted in adults
E. May be used for temporary or permanent pacing
83. Complications of extra-corporeal circulation include:
A. Haemolysis, anaemia and thrombocytopaenia
B. Excessive post-operative bleeding
C. Platelet dysfunction
D. Air embolism
E. Dissection of the aorta or femoral artery
16
84. In the examination of a 10-year old boy a systolic murmur is heard in
the left
sternal border with maximal intensity in the 3rd interspace; the
pulmonary second sound is widely split.
The most likely diagnosis is:
A. Congenital aortic stenosis
B. Atrial septal defect
C. Ventricular septal defect
D. Patent ductus arteriosus
E. Congenital pulmonary stenosis
85. Myxomas
A. Are the most common primary tumor of the heart in adults.
B. Typically arise in the right atrium along the interatrial septum.
C. Sporadic cases of myxoma are almost always single.
D. Are benign but exhibit malignant behaviour.
E. Medical treatment is superior to surgery in children.
86. Risk factors for acute renal failure after cardiac surgery include:
A. Young age.
B. Baseline renal dysfunction.
C. Left ventricular dysfunction.
D. Peripheral vascular disease.
E. Clinical signs of poor cardiac function
87. In acute aortic dissection:
A. Presentation within the first 2 days is termed acute.
B. The term chronic is reserved for those patients presenting at greater
than 2
days following the initial event.
C. Stanford type A dissection include dissections that involve the
ascending aorta,
arch, and descending thoracic aorta.
D. De Bakey type I involves the ascending aorta.
E. Stanford type B dissection include dissections that originate in the
descending
thoracic and thoracoabdominal aorta
17
.
88. The risk of rupture presented by an enlarging aortic aneurysm may
be
described by the following:
A. Wall tension decreases as the radius of an aneurysm increases.
B. Larger aneurysms have a higher rate of expansion.
C. There is a 40-fold increased risk of rupture or dissection in an
aneurysm 6.0-6.9
cm in diameter compared to an aneurysm 4.0-4.9 cm in diameter.
D. Patients with Marfan syndrome have accelerated aneurysm growth and
tend to
rupture or dissect at smaller sizes.
E. Dissections are associated with an accelerated rate of expansion and
rupture.
89. The aetiology of AV block includes:
A. Ischemic heart disease.
B. Bacterial endocarditis.
C. Cardiomyopathy.
D. Iatrogenic.
E. Systemic lupus erythematosus.
90. In the normal heart, stroke volume is augmented 5-15% by AV
synchrony
versus the asynchronous state. The quantitative importance of AV
synchrony
increases in:
A. Left ventricular hypertrophy
B. Diastolic dysfunction
C. Heart failure
D. Dilated cardiomyopathy
E. Mitral stenosis
91. The mitral valve:
18
A. Has two leaflets, the aortic leaflet and the mural leaflet
B. The anterior leaflet is also known as the aortic leaflet
C. The mural leaflet annulus is intimately related to the circumflex
coronary artery
D. Is the most susceptible to rheumatic valvulitis
E. Is so named because of its resemblance to the bishop’s headdress
92. The aortic arch laterality (sidedness) is determined by:
A. The first branch
B. Which side of the body the aorta descends en route to the abdomen
C. The direction of the arch in the superior mediastinum
D. The bronchus over which it arches
E. The side of the ascending aorta
19
C. Hypocholesterolemia
D. Sedentary lifestyle
E. Smoking
97. Causes of aortic regurgitation include:
A. Aortic valve endocarditis
B. Ascending aortic aneurysm
C. Type A aortic dissection
D. William’s syndrome
E. Rheumatic heart disease
98. Aortic stenosis:
A. May result from syphilitic aortitis
B. Can cause sudden death
C. Is characterized by the angina pectoris without coronary artheroma
D. Becomes significant only when the transvalvar gradient reaches
100mmHg
E. Causes syncope
20
CHAPTER 26
THE HEART
ANSWER
1. A, C, D 36. C 71. E
2. B, E 37. C 72. D
3. B, D 38. A, E 73. A, B,
C
4. A, C 39. A, B, C, E 74. D
5. D 40. B, C, D 75. A, B, C, D, E
6. B 41. A, C, E 76. A, B, C, D, E
7. C, D 42. A, B, C, D, E 77. A, C
8. D 43. B 78. A, B, C, D,
E
9. A, C, E 44. B, C, D 79. A, B, C, D, E
10. B, C, E 45. C 80. A, B,
11. A, B, C, D, E 46. A, B, E 81. A, B, C, D, E
12. A, E 47. A, B, C, D, E 82. A, B, C, E
13. B, C, D 48. A. C. D 83. A, B, C, D, E
21
14. A, B, C, E 49. A, B, C, D, E 84. B
15. B, C, D 50. A, C, D, E 85. A, C
16. A 51. B, C, E 86. B, C, D, E
17. C, E 52. A, B, C, D, E 87. A, C, D, E
18. B, C, D, E 53. D 88. B, D, E
19. A, B, D, E 54.A, B, C, D 89. A, B, D, E
20. A, B 55. A, B, C, D, E 90. A, B, C, D, E
21. B, C 56. A, B, C, D, E 91. A, B, C, D, E
22. A, D 57. A, B, D 92. D
23. B, C, D. E 58. A, B, D 93. C
24. A, D, E 59. A, B, C, D, E 94. A, C, D
25. E 60. A, B, D, E 95. D
26. A, B, C, D, E 61. A, B, C, D, E 96. A, D, E
27. B, C, D, E 62. A, B, C, D, E 97. A, B, C, E
28. A, B, C, D, E 63. A, B, C, D 98. B, C, E
29. A, B, D 64. A, B, C 99. A, B, C, D, E
30. A, B, C, D, E 65. D, E 100. B, C, D, E
31. B, C, E 66. B
32. A, B, D, E 67. C
33. A, C, D 68. C, D, E
34. B 69. A, B, C, D
35. B 70.A, B, C
22
CHAPTER 50
VASCULAR AND LYMPHATIC SYSTEMS
A. Thick
B. Relatively acellular
C. Non-wettable
D. Nourished via the vasa vasorum
E. Supplied by nerves
2. The media of an artery is:
Composed of fibro-elastic tissue and smooth muscle
Relatively thin but responsible for the strength of the arterial wall
In big arteries composed predominantly of muscle fibres
Nourished by the vasa vasorum
Separated from the adventitia by the internal elastic lamina
3. The veins:
Have the same capacity as the arteries
Have a wall consisting of muscle and fibro-elastic tissue
With the exception of the abdominal ones have valves which allow the
blood to flow only towards the heart
In the body cavities allow blood to flow as a result of the negative
pressure in the chest during respiration
Have sympathetic nerve supply
4. Where facilities exist, the investigations that MUST be done in every
patient
with peripheral arterial disease include:
1
Embolism
2
10. In atherosclerosis:
Lipids are deposited in the deeper layers of the intima
to form plaques
Plaques may become calcified or fibrosed
There is ulceration of the endothelium
The internal elastic lamina is thickened
The muscle of the media is replaced by fibrous tissue
3
Is probably an allergic reaction to nico-tine and regresses if smoking
is stopped
15. In thrombo-angiitis obliterans:
A. There is initial dense round cell infiltration of the adventitia
and media
B. There is endothelial proliferation of the intima
C. The lumen is occluded by a thrombhus which is later replaced by
firm granulation tissue
D. The lumen is never canalized
E. The artery or vein becomes enclosed in fibrous tissue
4
Patient is asleep
19. Signs of incipient gangrene of the foot include:
Coldness and numbness
Ulceration
Brittle nails and thin, shiny, hairless skin
Cyanosis of the toes
Absence of popliteal or dorsalis pedis pulse
A. The lower the level at which pallor of the sole appears when the leg is
elevated, the more severe the occlusion
B. Red discoloration of the sole when the leg is hanging suggests that
the ischaemia is not severe
C. A bruit at a particular site is due to dilatation of the artery above
the site of obstruction
Absence of the femoral pulse in both limbs is always indicative of
occlusion of the terminal aorta
Muscles of the affected limb are not wasted
21 In patients with chronic arterial occlusion of the lower limb:
About 40% improve spontaneously
About 55% remain unchanged
Only 5% require operation
Amputation is required in about 90% of those requiring operation
About half die within 5 years usually from C.V.A. or coronary
Thrombosis
22. In the medical management of chronic arterial occlusion of the
lower limb:
5
Smoking should be reduced
Fat intake should be low and the fat can be polysaturated
Leg exercises may increase the claudication distance by 8% and
improve
the physical and psychological state
Walking should be slow
23. Indications for operative treatment in chronic arterial occlusion of
the lower limb include:
Intermittent claudication
Rest pain
Inability to walk more than 150-200 m
Pregangrene
Absent popliteal pulse
A. Dacron
B. Autogenous artery
C. Autogenous saphenous vein
D. Glutaraldehyde stabilized umbilical vein
E. Nylon
25. Synthetic graft:
6
27. A cervical rib:
A. Right atrium
B. Infarcted myocardium
C. Aneurysm
D. Deep venous thrombosis
E. Subacute bacterial endocarditis
30. Common sites where a systemic embolus may lodge include:
7
A. Is swollen
B. Is infected
C. Is black
D. Has shriveled skin
E. Develops a red line of demarcation between the living and
dead tissue in a few days
33. In moist gangrene the affected part:
A. Is macerated
B. Always develops a red line of demarcation between the living and
and dead parts in a few days
C. Is green or black
D. Is not usually infected
E. Is not swollen
A. Aortic arch
B. Popliteal
C. Thoracic aorta
D. Femoral
E. Terminal abdominal aorta
37. Clinical features of an aneurysm include:
8
B. Marked pulsation
C. A thrill and systolic bruit over it
D. Reduction in the size and pulsation of the swelling when the artery
is compressed distal to the swelling
E. A smaller pulse distal to the swelling than on the contralateral side
38. In aneurysm of the abdominal aorta:
A. Hypertension
B. Peptic ulcer
C. Mitral incompetence
D. Hydronephrosis
E. Ischaemic heart disease
42. In the treatment of abdominal aortic aneurysm:
9
A. Excision of the aneurysm and replacement with a dacron graft is
preferred to an inlay tube graft
B. Aggressive fluid and electrolyte therapy including infusion of
mannitol is essential
C. Ischaemia of one or both limbs may occur post-operatively
D. The mortality in elective cases is only about 2%
E. About 50% of patients surviving operation are alive at 5 years
43. Renal artery stenosis:
10
superficial veins
B. Integrity of the osseo-fibrous compartment of the limb
C. Contraction of the veins
D. Contraction and power of the muscle bulk
E. Negative pressure in the abdominal cavity
47 The long saphenous vein:
11
Incompetent sapheno-femoral valve
51. Skin changes in varicose veins include:
53. A 40-year old woman has varicose veins of the right leg. When the
leg
is elevated with her in the recumbent position, the veins do not
collapse.
The cause of the varicosity may be:
Competent of the valves of the saphenous veins
Deep venous thrombosis
Incompetence of the sapheno-femoral valve
A pelvic tumour
Obstruction of the femoral or external iliac vein
54. If in the Brodie-Trendelenberg test, the varicose veins fill up from
below
immediately the patient stands up and before the tourniquet is
removed,
then the:
12
There must be obstruction in the deep veins
55. If in the Brodie-Trendelenberg test, the varicose veins do not fill up
when the
patient stands up from above when the tourniquet is released then
the:
58. The factors that maintain adequate venous circulation in the lower
limb
include:
13
Intra thoracic negative pressure maintenance
59. Varicose veins represent dilatation, elongation and tortuosity of
which
component of the lower limb venous system principally?
14
D. Uncomplicated (Early) varicose veins
E. Peripheral neuritis
F. Disc lesion – L4/5
G. Peripheral arterial embolism
62. How should this lady’s symptoms be best investigated:
15
65. A 40 year old diabetic man presents with recurrent itchy,
eczematous lesion
of his Rt. leg in the garter area, of nine months duration. He has
recently
experienced paraesthsia with recurrent breakdown of the skin. On
examination there is an ulcer just above the medial molleolus, with
shallow
sloping edges, firm, fibrotic base, depicting exuberant
granulations. There
are no varicose veins evident but there is a positive sapheno
femoral reflux
with a saphena varix.
16
69. Bleeding from a varicose vein is:
A. Pregnancy
B. Thrombo-phlebitis
C. Small varicose veins with competent valves of the communicating
perforators
D. Small varices following definitive surgery
E. Varicose veins with associated ulcer
72. The sclerosants currently in use for sclerotherapy of varicose vein
include:
A. Sodium morrhuate
B. Hydrocortisone in almond oil
C. Phenol in almond oil
D. Myodil
E. Sodium tetradecyl sulphate
73. The operative treatment of varicose veins:
17
as ulceration
C. Should in most cases be combined with Cockett’s operation
D. Has a mortality of about 1%
E. Has an average recurrence rate of less than 10%
74. What is the immediate treatment for the patient with varicose veins
complicated by acute bleeding from the region of the ankle?
18
78. The indications for operative management of varicose veins include:
Major varicosities
Incompetent perforators
First bleeding episode per se
Saphenofemoral incompetence per se
First episode of ulceration
Complication with superficial thrombophlebitis
Eczematous dermatitis
Ulcers – including grafting
Thrombophlebitis
Bleeding from varices
Chronic lymphoedema
80. The Cockets procedure (subfascial ligation of incompetent
perforators) is
indicated in all patients with:
A. Incompetent perforators
B. Recurrent varicose veins
C. Recurrent ankle ulceration and incompetent deep perforators at the
ankle
D. Incompetent perforators at the ankle
E. Varicose veins and chronic oedema
81. What instructions should be given to patients who undergo the
Trendelenberg operation for stripping of varicose veins.
19
veins
has been shown by recent Rendomised controlled Trials:
A. N. gonococcus
B. Wuchereria bancrofti
C. Chlamydia trachomatis
D. Haemophilus ducreyi
E. Herpes genitalis
85. Acute pre-or post-auricular lymphadenitis may be due to infection
of the:
20
86. External iliac adenitis or abscess:
A. Tuberculosis is the most likely cause if the age is under 10, and
and malignancy the most likely in those over 50
B. A short history is suggestive of acute infection and a long history
of chronic infection or malignancy
C. In the groin, pain is suggestive of acute inflammation, L.G.V. or
tuberculosis and absence of pain of malignancy or syphilis
D. Fever, malaise and myalgia are suggestive of acute or chronic
infection and not malignancy
E. Enlarged modes in the posterior triangle with a transient rash should
In endemic areas raise a suspicion of trypanosomiasis
88. In Lymphadenopathy:
21
maybe due to acute leukaemia
89. Investigations that will be useful in a 45-year old man with a 3-
month
history of enlarged lymph nodes in the right anterior triangle of the
neck
and a negative full clinical examination include:
A. V.D.R.L
B. Plain chest X-ray
C. Full blood count and E.S.R.
D. Blood film for microfilariae and aspiration of an enlarged node
E. Biopsy of an enlarged node
90. Lymphoedema:
A. Is accumulation of excessive amounts of interstitial fluid due to
inadequate
drainage as a result of obstruction of the lymph vessels
B. Affects the skin primarily
C. May also affect the muscles
D. Affects dependent parts of the body
E. Is primary if it is due to congenital mal-development of the lymph
vessels
91. Below-knee lymphoedema in a woman of 30 years in West Africa is
likely
to be due to:
22
A. Lymphoedema praecox
B. Trauma to the thigh
C. Tuberculosis of the inguinal nodes
D. Brugia Malayi
E. Metastases in the inguinal lymph nodes
93. Lymphoedema of the vulva alone in a 40-year old woman in West
Africa
is likely to be due to:
A. Lymphogranuloma venereum
B. Tuberculosis of the inguinal nodes
C. Chronic pyogenic sepsis of the vulva
D. Lymphoedema tarda
E. Wuchereria bancrofti
94. Lymphoedema of a breast in a 40-year old woman in West Africa
is likely to be due to:
A. Brugia malayi
B. Tuberculosis of the axillary lymph nodes
C. Lymphodema congenital
D. Axillary node metastases
E. Recurrent infection
Narrow and the lowest vertical nodes are not outlined while the
vessels
from the thigh and their corresponding nodes are normal, then the
cause is chronic sepsis
Dilated and tortuous and the nodes are not visualized, then
tuberculosis
Is the likely cause
23
Dilated and tortuous and the nodes are blocked or dilated, then the
likely
cause is filariasis
Not visualized, then aplasis is the most likely cause
Increased in number, caliber and tortuosity, then congenital varicose
dilation is the cause
97. Lymphoedema of the scrotum:
A. Is usually seen between 20 and 60
B. Is invariably accompanied by hydrocele
C. Does not usually involve the penis
D. May be associated with tiny vesicles of the skin of the scrotum
E. May be secondary to urinary fistulae
98. Unilateral lymphoedema of the lower limb in a 45 year old woman
should
be differentiated from:
24
best cosmetic result
B. Breast, amputation should be done
C. Vulva, antibiotics and diuretics suffice
D. Scrotum, excision should be done
E. Upper limb, amputation should be done
101. The histological types of Hodgkin’s lymphoma include:
A. Lymphocytic predomdinant
B. Nodular sclerosis
C. Histio-cytic predominant
D. Mixed cellularity
E. Lymphocyte depleted
102. Hodgkin’s disease:
A. Is pathologically characterized by the presence of giant cells
B. Is distributed throughout the world
C. Occurs in the third decade and over
D. Is “curable”
E. Is granulomatous rather than neoplastic
103. Hodgkin’s disease may present:
A. Most commonly as cervical or supraclavicular lymphadenopathy
B. As persistent pyrexia of unknown origin or cyclic fever
C. Often with paraplegia
D. With weight loss, lassitude or pruritus
E. With an abdominal “mass”
25
C. Lower extremity lymphangiogram
D. Lymph node biopsy
E. Staging laparotomy with splenectomy
106. In the Ann Arbor clinical staging of Hodgkin’s disease:
A. Stage I is limited disease of a single lymph node region or a single
extra-lymphatic organ or site
B. Stage II is involvement of 2 or more lymph node regions on the same
side of the diaphragm (II) or localized involvement of extra-lymphatic
organ or site and of one or more lymph node regions on both sides
of the diaphragm (IIE)
C. Stage III is involvement of lymph node regions on both sides of the
diaphragm (III) which may be accompanied by localized involvement
of the spleen (IIIS) or by solitary involvement of an extra-lymphatic
organ (IIIE) or both (IIISE)
D. Stage IV is diffuse or disseminated involvement of one or more
extra-lymphatic
organs or tissues with or without associated lymph node involvement
E. Lymphangiogram must be done in all cases
107. In the treatment of Hodgkin’s disease:
A. Stage I is treated by radiotherapy
B. Stages II is treated by radiotherapy and chemotherapy
C. Stages III and IV are treated by chemotherapy
D. The chemotherapy has been 6, 2-weekly cycles utilizing nitrogen
mustard,
vincristine, pro-carbazine and prednisone followed by a 2-week rest
period
E. Long-term disease-free remissions have been obtained in over 90%
of previously untreated patients
26
A. Block dissection is done for Stage I
B. Radiotherapy is used for Stage I disease
C. For Stages III and IV, the trend is to use radiotherapy and cyclical
chemotherapy
D. Currently, cyclophosphamide, vincristine and prednisone are given
every
21 days for 6 courses
E. Prognosis is best in the well-differentiated histiocytic lymphoma
110. Burkitt’s tumour:
A. Is the commonest malignant neoplasm in children in Africa
B. Does not occur outside of Africa
C. Occurs in epidemic form in parts of Africa
D. Has a high incidence across Africa within a belt 10-15˚ north and south
of the equator below 1500 m in altitude
E. Has the highest age incidence in both sexes between 4-12 years with
a
median age at 7-8
111. The histology of Burkitt’s lymphoma shows:
A. Lymphoctes-poorly differentiated
B. Undifferentiated lymphoreticular stem cells
C. Eosinophils
D. Histiocytes-well differentiated
E. Macrophages with abundant clear cystoplasm
112. Burkitt’s tumour presents most commonly as:
A. Cervical lymphadenopathy
B. Ascites
C. Painless progressive enlargement of one or more jaw quadrants
especially of the maxilla
D. An Abdominal mass
E. Flaccid paraplegia
27
C. Lungs, salivary glands
D. Subcutaneous tissues, long bones
E. Thyroid
115. Essential investigations in every confirmed case of Burkitt’s
lymphoma
include:
Liver biopsy
Intravenous pyelogram
Lumbar puncture for CSF cytology
Staging laparotomy and splenectomy
Bone marrow aspiration for cytology
116. Currently, the treatment of choice of Burkitt’s lymphoma without
CNS
involvement is:
A. Radiotherapy
B. Surgery for localized tumour
C. Cyclophosphamide administered as a single large dose of 40 mg/kg
I.V. and repeated for 4 courses at 2-3 weekly intervals
D. Methotrexate administered as a large dose I.V. followed by citrovorum
factor 24 h later
E. Cyclical combination chemotherapy with cyclohosphamide, vincristine
and methotrexate at 2-3 weekly intervals
117. It has been advised that following successful induction therapy in
Burkitt’s
lymphoma, there should be:
A. Blood transfusion
B. Monitoring of serum electrolytes and blood urea
C. Monitoring of blood uric acid
D. Administration of antibiotics
28
E. I.V. fluid therapy
119. In the prognosis of Burkitt’s lymphoma:
A. Long-term survival varies from 40-65%
B. About 50% of those showing remission have a relapse
C. Over 80% of those showing relapse have C.N.S. involvement
D. Chemotherapy has not been effective in relapse
E. Serum from cured patients has given favourable response in replapse
120. Sabfasical endoscopic perforator surgery has:
A. Proven a veritable minimally invasive alternative to open surgery
Lower recurrence rate to conventional open surgery
A higher neovascularization rate than conventional open surgery
A lower rate of failure to ligate long saphenous vein tributaries
A high success rate in locating and ligating significant perforators
121. Infective agents that have been implicated in the etiology of
lymphomas
include:
A. Helicobacter pylori
B. Human herpes virus-8
C. Hymenolepis nana
D. Hepatitis A
E. HTLV type I
122. The following are true of Hodgkin’s lymphoma:
123. In a patient with stage IIA Hodgkin’s Lymphoma you would expect:
29
D. Involvement of two or more lymph node regions on the same side
of the diaphragm
E. Unexplained fever
124. Gastric MALT lymphoma:
CHAPTER 50
VASCULAR AND LYMPHATIC SYSTEMS
ANSWERS
1. B, C 38. B, E 75. A, B, C, D, E
112. C, D, E
2. A 39. D 76. C
30
113. A, B
3. D, E, 40. E 77. B
114. A, B, D, E
4. A, C, D, E 41. A, B, D, E 78. A, B
115. B, C, E
5. C 42. B, C, E 79. A, B, C, D, E
116. C
6 A, D, E 43. B, C, E 80. C
117. E
7. C 44. C, D 81. C
118. A, B, C, E
8. A, B, D 45. C 82. A
119. A, B
9. C 46. B, D 83. A, E
120. C
10. A, C, E 47. A, D 84. A,B, C, D, E
121. A, B, E
11. A, B, C, D 48. C, E 85. A, D
122. B, D
12. B, C, E 49. A, B 86. A, B, C, E
123. B, D
13. A, C, E 50. E 87. B, E
124. A, B
14. C 51. A, B, C, D 88. A, C, E
125. A, C, E
15. A, B, C, E 52. A, C, D 89. B, C, E
16. A, B 53. B, D, E 90. A, D, E
31
CHAPTER 51
1
9
10
11
2
Which investigation will confirm the diagnosis?
Blood film
X-ray of the tibia
Hb electrophoresis
White cell count
Venogram
You will advise:
Ambulatory treatment with bandaging
Application of bland antiseptics and bed rest
Surgical debridement and grafting
Application of viscopaste to the leg
Dressing with Solcoseryl
A girl of 18 with Hb SC disease presented with acute
respiratory distress, cough and frothy sputum and soon after
admission became drowsy. On examination, the temperature
was 37˚C and there were petechial rashes on both arms; there
were no pulmonary signs.
3
Bronchoscopy
Pleural tap
Radioactive Xenon scan of the chest
Examination of the urine for fat globules
ECG
4
patient?
Osteochondritis dissecans
Subchondral and central sclerosis
Coxa vara
Flatening and irregularity of the femoral head
Milkman’s fracture
5
of 30
Is frequently marked by muscle tenderness
In its abdominal form may be indistinguishable from pancreatitis
Reticulocytosis ranging from 10-15% may be associated with it
In sickle cell disease:
Not all patients are found to be anaemic
Symptoms only begin to manifest after 3 months of life
The average (steady state) Hb level for SC patients is 8g/dl
The most severe anaemia occurs with SB thalassaemia
Growth disturbance may produce a stunted figure, much below
average weight
6
An attack of falciparum malaria
Typhoid fever
Sequestration syndrome of sickle cell disease
Splenic infarct
Viral hepatitis A
The most useful diagnostic investigation is:
Plain x-ray of the chest-erect
Plain x-ray of the abdomen-erect
Abdominal ultrasound
Liver function tests
A full haematological profile
7
The most likely diagnosis is:
Recurrent attacks of malaria
Recurrent attacks of typhoid
Osteomylitis of the left tibia
Hand foot syndrome of sickle cell disease
Attacks of Dengue fever
The most useful diagnostic test is:
Blood film for malarial parasites
Blood culture
A full haematological profile
Chest x-rays
Liver function tests
8
patients blood count is reported as “Total WBC 40,000/cub
mm, including normoblasts with reticulocystosis – 12%.
9
11gm/dl
12gm/dl
The average steady state Hb maintained by patients with Sickle
Cell disease (Genotype SC) in the typical socio-economic
circumstances in West Africa is:
8-9gm/dl
10-11gm/dl
12-13gm/dl
14-15gm/dl
16gm/dl
10
Haemolytic jaundice attendant on repeated episodic sickle cell
crises
Hepatocellular Jaundice – Hepatitis A
Hepatocellular jaundice – Hepatitis B
The test most likely to clinch the diagnosis is:
Percutaneous Transhepatic Cholangiography (PTC)
Endoscopic retrograde Cholangiopancreatogrophy (ERCP)
Magnetic Resonance Cholangiopancreatogrophy (MRCP)
Hepatic Scintigraphy
Helical CT Scan of the abdomen
The treatment for the patient in Question 32 is:
Resuscitation + adequate nutritional supplements
Resuscitation + check on G6PD status and review of charted
drugs given
Bed rest and attention to urgent nutrition needs
D. Resuscitation + monitoring for signs of progression and need for
surgical
intervention
E. Resuscitation, I/V administration of 10% fructose, Vitamin. K and
prophylactic antibiotics
11
splenism in a patient with splenomegaly in Sickle Cell Disease,
and therefore requiring splenectomy?
The spleen is > 4cm below the Lt. costal margin
The HB falls < 6.5g/dl
The reticulocyte count exceeds 15%
The platelet count falls below 200 x 109/l
None of the above
A man of 25 presents in the Emergency Room with a sudden
onset of severe pain in the left hypochondrium, much
worsened on inspiration. He is a pyrexial, and anicteric; his
chest is clear and has a tender mass that moves with
respiration in the left hypochondrium. There have been no
previous attacks:
12
May be due to viral hepatitis
Is attended by the morbid anatomical change of sinusoidal
engorgement with fibrin clots
Is marked by central lobular parenchymal necrosis
Is very frequently attended by jaundice of obstructive
intrahepatic type
May be accompanied by fever, leucocytosis and abdominal pain
Hepatomegaly in sickle cell disease:
Is frequently associated with extrahepatic ductal obstruction by a
stone
Is attended by sinusoidal haemosiderosis
May be associated with biliary canalicular thrombi
May on occasion be an indication for laparotomy
Is often seen with anasarca
Jaundice in sickle cell disease:
Is most frequently acholuric arising from excessive red cell
destruction
May produce an elevation of both direct and indirect reacting
bilirubin
May be difficult to distinguish from extrahepatic ductal
obstruction
May on occasion be an indication for laparotomy
Should initially be treated conservatively with adequate fluids
and nutritional supplements
13
Is characteristically reduced to a small nubbin of fibrous tissue in
adolescent SS patients
Is seldom reduced in size in patients with SC disease
May occasionally require removal as a measure to reduce
frequency of haemolytic episodes
The kidney in sickle cell disease:
May show defective tubular concentration in the form of
hyposthenuria
Has a tendency to excessive concentration of urine
Is often grossly enlarged (symmetrically)
Need not be investigated for other causes of haematuria in
patients presenting with haematuria
If the source of unilateral presistent bleeding may require
surgical excision
Haematuria in sickle cell disease patients:
Occurs in 2-4% of Hb SS and Hb SC patients
Is more likely to arise from causes other than the sickling lesion
in the kidney
May be prolonged and recurrent and usually painless
Is treated with blood transfusion, alkaline infusions and
occasionally aminocaproic acid
May warrant a nephrectomy if unilateral and persistent
14
Arises usually from ulcerations of the renal papillae, the result of
papillary infarct
Is likely to be persistent because of constant contact of the
ulcerating lesion with urokinase
Is usually total and recurrent
May be treated by blood transfusions, alkaline infusions and
diuretics
Is never life threatening enough to warrant nephrectomy
The recurrent haematuria which occurs in some 2-4% of patient
with Sickle Cell disease (Hb SS and SC) arises from:
Ulceration of the tips of the renal papillae
Infarction in the medulla of the kidney
Sickling phenomena in the cortex of the kidney
Ulceration in the trigone of the bladder
Infacts of the mucosa of the renal pelvis
The bleeding in Sickle Cell haematuria becomes repetitive and
persistent because:
Of repeated episodes of sickling crisis
The hyposthenuria that accompanies Sickle Cell disease
Febrinolytic enzymes (urokinase) being continuously in contact
with
the urine
High pH of the urine in Sickle Cell disease
Attendant urinary tract infection
The first line management in Sickle Cell patients with
haematuria is:
Intravenous infusion of alkalinizing agents (NaHCO3)
Blood transfusions
Administration of diuretic agents
Infusions of Amino caproic acid
15
Infusion of ringers lactate
16
Should be treated by bed rest and wound dressing with mild
antiseptics
17
B. Is more often than not associated with varicose veins with
incompetent
perforatiors
Is usually deep seated with exposure of muscle, tendon and
periosterum
Shows no stratification of incidence in socio economic groups
Is frequently complicated by malignant degeneration
18
A. Is seldom a cause for a crisis
B. Occurs as frequently as in the general population
C. Characteristically affects the lower lobes
D. Is common because of pulmonary congestion, thromboses and
impairment of immunity on account of autosplenectomy
E. Is often complicated by cardiac arrhythmias and right heart failure
19
capillaries of periphery of fundus
C. Retinal, choroidal and anterior uveal infarcts
D. Micro-aneurysms, dilated capillaries and veins
E. Proliferative neovascularization of the vitreous from which vitreous
haemorrhages may occur
62. Ocular changes in sickle cell disease may take the form of:
A. Heightened flow in the arterioles of the fundus with silver wiring
appearance
B. Ischaemic areas showing whitening of the retina
C. Haemorrhages of varying severity which may be retinal, peri-
retinal
D. Neovascularization of the retina, budding capillaries, a
compensatory
reaction to retinal ischaemia
E. Tears and detachment of the retina
20
64. In the management of patients with sickle cell disease:
A. Blood transfusion is more useful than alkaline infusions in
decreasing
the sickling tendency
B. Oxygen therapy has no immediate effect on the sickling process
C. Prophylactic antimalarial therapy is of proven benefit
D. Prophylactic Vit. B12 has been found beneficial
E. Efforts should be made to achieve pre-operative Hb levels of 12
g/dl
in adults
65. In the management of patients with sickle cell disease:
A. Expanding the plasma volume using alkaline and dextrose
infusions
decreases the sickling tendency
B. Oxygen therapy relieves the pain and other distressing
symptoms
accompanying crises
C. Search for and prompt treatment of acute infections may abort a
crisis
D. Anticoagulants such as Arvin may prove useful in aborting or
arresting
an attack
E. Efforts should be made to achieve pre-operative Hb levels of 10
g/dl
in children
21
D. Take the form of the classic cod-fish appearance
E. May take the form of collapse of the vertebral bodies
67. The pathological changes of sickle cell disease affecting the
hip:
A. Are common and indistinguishable from Perthes’ disease
B. Are more common in Hb SS patients than SC or other varieties
C. Are usually related to some sepsis in the upper end of the
femur
or hip joint
D. May produce septic dislocation of the hip
E. May result in total sequestration of the femoral head
68. The pathological changes of sickle cell disease affecting the
hip:
A. Are rare and distinct from all childhood hip affections
B. Usually results in bony ankylosis
C. Are nearly always the result of early experience of trauma to the
hip
D. Are frequently arrested by prolonged bed rest with the affected
limb
in traction
E. Are seldom bilateral
69. The head of the humerus in sicklers:
A. Is notably subject to infarction though not as frequently as the
femur
B. Does not deform as badly as the femoral head
C. Is more liable to develop early osteoarthritis than in the normal
population
D. Usually escapes early osteoarthritis
E. Showing avascular necrosis is best treated by short wave
diathermy
and mobilization exercises
70. Osteomyelitis in sickle cell disease:
22
A. Affects nearly 90% of Hb SS patient in one or more bones
before
the age of 10
B. May start anywhere along the shaft of the long bone
C. Usually starts in the metaphysis and spreads down the
diaphysis
D. Has a less stormy course than in the Hb AA patient
E. Should be treated by parenteral ampicillin and cloxacillin
71. Osteomyelitis in sickle cell disease:
A. Affects nearly 50% of Hb SS patients in one or more bones
before
the age of 10
B. Not uncommonly produces segmental lesions along the shaft
of the same bone
C. Is most frequently produced by staph. pyogenes
D Is frequently complicated by septicaemia
E. Should be treated by oxygen therapy, antibiotics, limb
immobilization
and timely evacuation of intramedullary pus
72. For children with Sickle Cell disease the principal cause of
post
operative morbidity and mortality is:
A. Acute chest syndrome and splenic sequestration
B. Post operative malaria
C. Dehydration
D. Urinary tract infection
E. Low Hb in the post operative period Hb < 8.0g/dl
73. In patients with Sickle Cell disease undergoing operation it
is generally
recommended that to obtain the normal P02 tension in the
system the
oxygen ventilation during surgery should be at least:
23
A. 20%
B. 25%
C. 30%
D. 35%
E. 40%
CHAPTER 51
ANSWERS
1. A 38. C
2. A, B, C, D, E 39. A, B, C, E
3. D 40. B, C, D
4. B 41. A, B, C, D, E
5. A 42. A, B, C, D, E
6. A 43. A, C, E
7. D 44. A, B, C, D, E
8. C 45. A, B, C, D
9. C 46. A
10. D 47. C
11. D 48. A
12. D 49. A, B, C, D, E
13. A, B, C, D 50. D, E
14. A, B, C, D 51. D
15. A, B, C, D 52. A, B, C, D, E
16. B 53. A, D, E
17. A, B, C, D, E 54. A, B, C, D, E, F
18. B, C, D, E 55. A
19. A, B, (D) E 56. A
24
20. C, D, E 57. C
21. C 58. A, B, C, E
22. E 59. C, D, E
23. C 60. A, B, C, D, E
24. D 61. A, B, C, D, E,
25. C 62. B, C, D, E
26. D 63. B
27. E 64. C
28. A 65. A. B, C, E
29. D 66. A, B, C, D, E
30. A 67. A, C, D, E
31. B 68. D
32. C 69. A, B, C, E
33. C 70. A, B, E
34. D 71. B, C
35. D 72. A
36. A, B, C, D 73. C
37. C
25
CHAPTER 43
SYMPTOMS, EXAMINATION, INVESTIGATION AND
INSTRUMENTS IN UROLOGY
Costo-vertebral angle
Loin
Ureteric pain:
Radiates from the tip of the 9th costal cartilage to the suprapublic
1
Usually causes referred pain in the skin of the lumbar region
Difficulty of micturition
Agonizing pain
Haematuria
Prostatic pain:
Urethral pain:
2
Difficulty is inability to void urine
elaborate urine
5 mmol/l
urography
3
excretion
of radioactive iodohippurate
Sugar
Crystals
Leucocyte casts
Protein
Calculi
4
Benign prostatic hypertrophy
Cystoscopy
Urethral catheterization
Stool examination
Inulin
Vit. B12
Creatinine
Urea
Glucose
Is self-retaining
5
Gibbon’s catheter:
Depezzer catheter:
Is not self-retaining
Is a suprapubic catheter
Filiform catheters:
Can be autoclaved
Sounds are:
6
Straight bougies
Not autoclaved
The cystoscope:
Lister’s bougies:
Are autoclaved
7
suggestive of:
Prostatic carcinoma
Vesical carcinoma
Vesical calculus
Bladder diverticulum
8
CHAPTER 43
SYMPTOMS, EXAMINATION, INVESTIGATION AND
INSTRUMENTS IN UROLOGY
ANSWERS
A, C, D
B, D, E
C, D
A, B, D
B, C
A, B, E
C, E
B, C
A, D, E
A, D, E
B, E
A, B, D
C
A
A, B, D
B, C
C
A, B, E
9
B, D, E
A, C, D
C, D
A, B, C
10
CHAPTER 44
ACUTE RENAL FAILURE, HAEMATURIA, HAEMATOSPERMIA
Acute renal failure:
Extra-renal failure:
1
Acute obstructive uropathy:
Entero-cutaneous fistula
Myocardial infarction
Radiation
Cortical necrosis
Pelvic neoplasia
2
Radiographic contrast media may cause renal damage
3
Acidosis in renal failure:
Pulmonary oedema
In peritoneal dialysis
Wound dehiscence
4
Polycystic kidneys
Recent laparotomy
In peritoneal dialysis:
Haemodialysis:
Disequilibrium syndrome:
5
Prevention is by slow but short periods of dialysis
The survival results after acute renal failure from tubular necrosis
is worse in:
Surgical patients
Non-surgical patients
ICU-patients
6
procedures
Haematuria:
due to:
Vesical schistosomiasis
Bladder calculi
7
Renal cell Carcimona
Prostatic calculi
Prostatitis
Schistosomiasis
Urethritis
VDRL is be indicated
Urethrocystoscopy is required
8
CHAPTER 44
ACUTE RENAL FAILURE, HAEMATURIA, HAEMATOSPERMIA
ANSWERS
9
A,C,D,E 25. A, B, C, D
A,B,C,D 26. A, B, C, D, E
A,B,C,D 27. A, B, C
A,B,D,E
A,B,C,D
A,B,C,E
A,B,D
B,D,E
C,E
A,B,C,D,E
C,D
A,B,C,D,E
A,B,C,D,E
A,B,D,E
A,B,E
A,B,E
A,B,C,E
C,E
A,C,E
A
10
A,C,E
B,C,D,E
A,B,C,E
B,E
11
CHAPTER 46
BLADDER, URETHRA AND PENIS
The bladder
When distended is separated from the lower anterior abdominal wall
by peritoneum
Has a well‐defined internal sphincter at its orifice
Orifice is closed by active contraction of the internal sphincter during
filling
Epithelium is transitional cell
Sensory nerves run chiefly through the sympathetic and end in T9 to
L2
The sphincter urethrae (external sphincter):
Surrounds the membranous urethra
Lies above the upper layer of the urogenital diaphragm
Has smooth muscle fibres
Is under voluntary control for interrupting or withholding urine flow
for short periods
Is innervated by the pelvic nerves which end in S2, 3, 4
When the volume of urine in the bladder is:
10ml the internal pressure is 5‐10cm of water
300ml bladder fullness is appreciated and there is a desire to
micturate
Over 450ml bladder contractions become regular and powerful with
an urgent desire to void
500 ml the contractions are continuous and very strong and the desire
to void continues
700‐800 ml the contraction is painful
In disorders of micturition:
The inhibited bladder has a small capacity and throughout filling
there are brief irregular contractions
The commonest cause of bed‐wetting in children is the uninhibited
bladder
Spinal cord transection causes permanent loss of voiding reflex
Cauda equine tumours cause permanent bladder flaccidiy and
distension.
All reflex contactions of the bladder are abolished and distension is
not appreciated.
In extrophy of the bladder
1
The rami of the symphysis pubis are close together
Coitus is not possible in both sexes because of the associated genital
anomalies
Closure of the bladder is the operation of choice
The incidence of carcinoma is higher than in the normal bladder
Most of the untreated patients die of pyelonephritis before 10years
Urachus may give rise to:
Umbilical sinus
Bladder diverticulum
A cyst
Vesico‐umbilical fistula
Bladder neck obstruction
The most likely clinical diagnosis is:
Carcinoma of the bladder
Pyelonephritis
Cystitis
Salpingitis
Urethritis
The MOST useful diagnostic investigation is:
Urinalysis
Culture of midstream urine and sensitivity test
Urethral smear for microscopy and culture
Cervical or high vaginal swab for microscopy
Cystoscopy
Bacterial cystitis
Is commoner in women because of their short urethra
Is always associated with a predisposing factor
Is most commonly caused by staph. Aureus
Most commonly affects the trigone and bladder base
Is initially best treated by oexytetracycline while sensitivity tests are
awaited
Interstitial cystitis:
Is a common chronic inflammatory condition seen in middle‐aged
women subjected to nervous strain
Causes deposition of fibrous tissue in the muscle bundles,
2
degeneration of muscle bundles and diminished bladder capacity
Presents with progressive severe frequency, nocturia and suprapubic
relieved by micturition
Usually yields Esch. Coli or other gram negative organisms on culture
of the urine
Responds well to antibiotics and steroids.
Parasitic diseases of the bladder include:
Entamoeba histolytica
Schistosoma japonicum
Trichomonas vaginalis
Onchocerca volvulus
Taenia echinococcus
The following may be seen at cystoscopy of a patient with urinary
schistosomiasis:
Tubercles
Carcinoma
Ulcers
Papilloma
Diverticula
Common complications of schistosomiasis of the bladder include:
Atonic distended bladder from chronic outlet obstruction
Vesical calculus
Pyelonephritis
Recurrent acute epididymo‐orchitis
Infertility
The commonest type of bladder diverticulum:
Consists of mucosa surrounded by muscle fibres
Originates from urachus
Empties easily into the bladder
May become larger than the bladder
May like other types of diverticula rarely become malignant
Bladder cancer:
Is the commonest G.U. neoplasm
Is more common in blacks than in Caucasians
In Africa has a high incidence in Southern Malawi and Coastal Kenya
Has a M/F ratio of 4‐5/1
Has the highest incidence in the 41‐ 50 age group
3
Bladder cancer is associated with:
Smoking
Asbestos industry
Dye, textile or mining industry
Urinary schistosomiasis
No obvious cause in most patients
Most bladder cancers:
Are sessile
Are in the bladder base
Are squamous cell in type
Are multiple
Have a tendency to recur
On bimanual examination under G.A. of a 60‐year old man with
suspected carcinoma of the bladder, a movable 2 cm mass with rubbery
consistency is found. The lateral ligaments are free
A . The tumour is likely to involve only the submucosa or superficial
muscular layer
B. The clinical stage is T2
C. The U.I.C.C. stage is T2a
D. Lymph node involvement is not likely to have taken place
E. The prognosis should be good
In the treatment of transitional carcinoma of the bladder:
AT1 tumour of the base is best treated by transurethral endoscopic
diathermy resection, but the recurrence rate is high
For severe widespread carcinoma in situ of the urothelium,
intravesical chemotherapy with thiotepa every 3 months is advocated
The U.I.C.C. stage is T2a well‐differentiated low grade tumour at the
base, radical cystectomy is indicated
For a T3 tumour, a combination of pre‐operative radiotherapy and
radical cystectomy gives a survival of 40% in 5 years
For a T4 tumour, systemic chemotherapy gives better results than
radiotherapy
A patient who has been treated for cancer of the bladder should be
followed up for:
6 months
1 year
5 years
10 years
The rest of his or her life
4
In the prognosis of carcinoma of the bladder the 5‐year survival:
Untreated patients is 5%
AT1 tumour with local diathermy resection is about 75%
AT2a tumour with partial cystectomy is 50%
A T2b tumour with radical cystectomy is 40%
T4 tumour with radiotherapy is nil
The fistula is
High vesico‐vaginal
Low vesico‐vaginal
Urtero‐vaginal
Urethro‐vaginal
Vesico‐uterine
The commonest cause of retention of urine in adult males in West Africa
is:
Urethral stricture
Bening prostatic hypertrophy
Prostatic carcinoma
Acute urthritis
Paraphimosis
Retention of urine:
If painless is likely to be chronic
If acute is associated with previous dribbling
May be caused at all ages in both sexes by bladder neck obstruction
If associated with haematuria in an old man is most likely caused by
bladder cancer
If sudden during micturition and associated with pain at the tip of the
penis or perineum is most probably caused by urethral stricture
In the anatomy of the male urethra the:
Membranous urethra is the most fixed and narrowest part
External urethral sphincter surrounds the bulbar urethra
Least dilatable part is the external meatus
Epithelium is stratified or pseudo‐stratified in the glans and
transitional proximal to the glans
Lymphatics drain into the inguinal nodes
Congential stenosis of the external urethral meatus:
Is rare
Occurs only in males
May cause bloodyspotting and crusting of the meatus
5
May cause renal failure
Is treated by regular urethral dilatation
Epispadias:
Is a congenital deformity in which the urethra opens on the dorsum
of the penis proximal to the glands
Is caused by failure of union of the anterior and posterior walls of the
urethra
Does not occur in females
Is associated with ventral curvature of the penis which is often short
Makes coitus impossible in most patients
Hypospadias:
Is not associated with urinary incontinence
Is commoner in females
If perineal, the male external genitalia resembles that of the female
If penoscrotal or perineal is associated with a miniature penis with
marked dorsal curvature
If glandular does not require any treatment
A 2‐year old boy has been having difficulty of micturition and dribbling for
over a year. On examination, he is cachectic and a distended bladder is
palpable. A urethral catheter is passed without difficulty.
The most likely clinical diagnosis is:
Stenosis of the meatus
Congenital non‐meatal urethral stricture
Phimosis
Posterior urethral valves
Bladder neck obstruction
The investigations that will establish the diagnosis include:
Excretory urography
Micturating cystourethrogram
Urethrogram
Urethrocystoscopy
Blood urea and serum electrolytes
Possible complications include:
Urinary fistulae
Bladder diverticula
Urinary tract infection
Hypertension
6
Unilateral hydronephrosis
Treatment will include:
Suprapubic cystostomy
Urethral dilatation
Urethroplasty
Loop ureterostomy
Meatotomy
A 25‐year old man in Singapore develops a thick yellow urethral discharge
and burning on micturition 5 days after sexual intercourse with a casual
companion
The organism(s) likely to be responsible is (are):
Chlamydia trachomatis
N. gonorrhoeae
Candida albicans
T. vaginalis
Esch. Coli
The most useful investigation is:
Culture of urethral discharge
Urine culture
Immunofluorescent antibody test
Microscopic examination of a urethral smeal (gram and methylene
blue stains)
VDRL
The treatment of first choice is
Ceftriazone 250 mg IM
Procaine penicillin G 3.8m
Azithromycin 500 mg daily for 3 days
Doxycycline 100mg bd for 7 dyas
Oxytetracycline 500 mg qds for 4 days
Symptoms persist in spite of treatment. Drugs to be recommended
include:
Ciprofloxacin 500 mg b.d. for 7 days
Chloramphenicol 2 g daily for 5 days
Azithromycin 500 mg daily for 3 days
Doxycycline 100 mg bd for 7 days
Erythromycin 500 mg qds for 10 days
7
Symptoms subside after 48h. But 24 days after the intercourse, a thin
watery discharge most marked first thing in the morning recurs. The
patient claims he has not had any sexual contact since treatment. The
discharge is due to:
Re‐infection
Chroniciy of the original infection
Prostatorrhoea or spermatorrhoea
Primary non‐specific urethritis
Secondary non‐specific urethritis
Useful investigations include:
Two glass urine test
Microscopy of urethral smear for polymorphs
Microscopy of gram‐stained urethral smear
VDRL
Urinalysis
The most likely organism is:
Gonorrhoea
Pencillinase producing N. gonorrhoeae
Esch. Coli
Cylamydia trachomatis
T‐strain mycoplasma
The drug of first choice is:
Doxycycline 100mg bd for 14 days
Tetracycline 250mg qds for 14‐21days
Procaine penicillin G 4.8m Im
Erythromycin 500mg qds for 7 days
Sulphasoxazole 2 g daily for 5 days
The most effective drug for pharyngeal gonococcal infection is:
Ampicillin
Amoxillin
Pivampicillin
Ceftriazone
Spectinomycin
Complications of gonococcal urethritis include:
Tenosynovitis
Meningitis
Encephalitis
Arthritis
8
Pyelonephritis
Causes of secondary non‐gonococcal urethritis include:
Urethral stricture
Urethral tumour
Urethral catheterization
Cystitis
Sexual intercourse
Urethral stricture may be caused by:
Primary non‐specific urethritis
Urethral instrumentation
Urethral calculus
Vaginal douching
Prostatitis
Urethral stricture
Following urethritis is formed within a year but takes on an average
20 years to become symptomatic
Following trauma becomes symptomatic in two months
Following urethritis is commonest in the penile urethra
May lead to extravasation of urine or be associated with carcinoma of
the urethra
Clinical cases are all of acquired origin
The most reliable investigation for the diagnosis of urethral stricture is:
Urethrogram and voiding cystourthrogram
Excretory urography
Passage of urethral metal bougie (22 Ch)
Urethroscopy
Cystoscopy
The I.V.P. of a 55 year old West African male shows bilateral
hydronephrosis and a high residual urine. Diagnosis may be:
Tuberculosis of the bladder
Benign prostatic hypertrophy
Carcinoma of the urethra
Urinary schistosomiasis
Carcinoma on the lateral wall o the bladder
In the management of urethral stricture, dilatation of the urethra:
Is curative
Is performed for passable incomplete strictures
9
For tight strictures is performed with small size metal bougies or
filiforms and flollowers
Is repeated at increasing intervals and stopped after 2 years
May cause septic shock
Internal urethrotomy:
Is splitting of a stricture under direct vision
Is suitable for long uncomplicated impassable strictures
Requires subsequent splinting of the urethra with an indwelling
catheter for 1 week
Gives permanent cure
Does not require subsequent dilatation
Urethroplasty:
Is indicated in complete strictures
Is curative in most patients
Is always done in 2 stages
May be complicated by fistulae … restenosis
May result in the formation of a hair‐ball in the urethra
In the initial management of the complications of urethral stricture:
Retention of urine may be relieved by suprapubic tap using a needle.
Extravasation of urine is managed by continuous bladder drainage via
a urethra catheter.
Fistulae require urgent urethroplasty
Uraemia necessitates suprapublic cystostomy and continuous bladder
drainage
Dilatation of the urethra is never done.
Primary carcinoma of the urethra:
Is most commonly transitional cell
Is best diagnosed by urethrogram
If confined to the distal half of the penis is treated by partial
amputation of the penis
In women is treated, if early, by localized interstitial radiotherapy
Has a poor prognosis even in early cases
A 30‐year old woman complains of dyspareunia, dribbling of urine after
micturition and a swelling in the anterior vaginal wall.
The most likely clinical diagnosis is:
Urethral caruncle
Urethro‐vaginal fistula
10
Carcinoma of the urethra
Diverticulum of the urethra
Prolapse of the urethra
Senile urethritis:
Is caused by Esch. Coli
Is associated with a dry pale vagina
Causes dyspareunia, frequency, vaginal and vulval irritation
Is diagnosed by urine culture and urinalysis
Is treated with sulphonamides or appropriate antibiotic
In the anatomy of the penis
The lymphatics of the penile skin and prepuce drain into the
superficial inguinal nodes
The lymphatics of the glans and corpora drain into the internal iliac
nodes
The nerve supply is from the genitor‐femoral nerve
The corpora consist of spongy saccules into which arterioles open
directly
Venous return is to the prostatic venous plexus, internal pudendal
and saphenous vein
Paraphimosis:
Is constriction of the prepuce
May be precipitated by sexual intercourse
Presents as pain and oedematous swelling of the glans and prepuce
May lead to gangrene of the prepuce and glans
Is treated by circumcision
A 35‐year old man who denies sexual intercourse in the past 6 weeks
presents with a punched out painless ulcer about 1cm in diameter on the
glans. The base of the ulcer is hard. The inguinal nodes on both sides are
palpable, discrete, non‐tender and hard.
The most likely clinical diagnosis is:
Lymphogranuloma venereum
Chancroid (soft chancre)
Syphilitic chancre
Epithelioma
Non‐specific ulcer
The most useful investigation is:
VDRL test
11
Biopsy
Microscopy: Fluorescent antibody dark‐field examination
Frei’s test
Treponema immobilization test
Treatment is:
Excision of the ulcer
Partial amputation of the penis and radiotherapy of the lymph nodes
Procaine penicillin 1 mega unit daily for 10‐14days
Sulphadiazine 1g qds for 10‐14days
Daily (eusol dressing)
Chancroid (soft chancre) is:
Caused by Haemophilus ducreyi
Always solitary and starts as a painful pustule
Reliably diagnosed by serological test
Common in the temperate and tropical regions
Treated with a sulphonamide for 5 days
Granuloma inguinale:
Is a chronic infection of the skin and subcutaneous tissues of the
genitalia, perineum or inguinal regions
Is caused by a virus
Starts as a pustule or papule which ulcerates
May lead to lymphoedema and urethral stricture
Is best treated with procaine penicillin 1 mega daily for 14‐21 days
Erosive and gangrenous balanitis:
Is caused by Borelia vincenti
Presents as erosions or painless irregularly shaped usually multiple
ulcers
Occurs in the circumcised and uncircumcised
Always spreads to the inguinal nodes
Is treated with penicillin or oxytetracycline for 7 days.
Herpes genitalis:
Is caused by herpes simplex virus type II
Starts as vesicles which rupture to form small round painful tender
erosions or ulcers
Is associated with painful enlarged inguinal lymph nodes
Does not recur
Is treated with oxytetracycline, chloramphenicol or ampicillin
12
Plastic induration of the penis (Peyronie’s disease):
Caused by calcification of the corpora cavernosa
Usually causes dorsal chordee
Is felt as well‐demarcated raised indurated plaque in the shaft
Is confirmed by biopsy
Is treated satisfactorily with vitamin E or low dosage radiotherapy
Priapism:
Is prolonged erection of the penis
Is most commonly caused in West Africa by SS disease
Requires a full blood count
May result in impotence
Is best treated by a venous shunting operation.
Carcinoma of the penis is common in:
Ethiopia
Uganda
Nigeria
Kenya
China
The incidence of carcinoma of the penis is:
Nil in communities where circumcision is done before the age of 12
years.
Is high among the uncircumcised of Zambia
Is high among uncircumcised Hindus
Is low among the uncircumcised in Mozambique
Is highest in the fifth decade
Carcinoma of the penis:
Occurs most commonly on the coronal sulcus
Is histologically transitional cell
Spreads early to the inguinal lymph nodes
Spreads rarely via the blood stream
Is of low grade malignancy in most patients
Carcinoma of the penis presents as:
Purulent discharge from the prepuce
Scalding
An ulcer with punched out edges
A lump under the prepuce
Urethral fistula
13
In the treatment of carcinoma of the penis:
A small stage 1 exophytic tumour on the coronal sulcus glans in a 40‐
year old man is treated by partial amputation of the penis
A small lesion localized to the prepuce in a 60‐year old man is treated
by circumcision
A stage II tumour involving the distal shaft in a 50‐year old man is
treated by total amputation
Enlarged mobile inguinal lymph nodes persisting 3 weeks after
treatment of the primary are preferably treated by bilateral ilio‐
inguinal block dissection
Bleomycin and methotrexate are effective in about 40 % of patients
Indications for suprapubic cystostomy include:
Acute retention of urine due to urethral stricture
Periurethal abscesses
Rupture of the urethra
Extravasation of urine
Contracted bladder due to tuberculosis
Indications for uretero‐ileal‐cutaneous diversion of urine (ileal conduit)
include:
Vesico‐vaginal‐rectal fistula
Contracted bladder due to schistosomiasis
Ectopia vesicae
Urethro‐cutaneous fistulae
Uncomplicated spina bifida
Complications of uretero‐sigmoidostomy include:
Pyelonephritis
Metabolic alkalosis
Hypokalaemia
Hyponatraema
Renal lithiasis
A plain X‐ray of the pelvis shows calcification in the bladder wall. The
cause may be:
Tuberculosis
Carcinoma
Hyperparathyroidism
Schistosomiasis
Atheroscierosis of the vesical vessels
Drugs effective against PPNG and non‐PPNG include:
14
Erythromycin
Ciprofloxacin
Ceftriazone
Ampicillin
Ofloxacin
77. The following are associated with extrophy of the bladder:
Waddling gait
Epigastric hernia
Urinary incontinence
Male to female ratio is 4 : 1
Bladder malignancy
78. The best time after birth to close extrophy of the bladder is:
Within 72 hours
Within one month
Before one year of age
At the time of puberty
After puberty
79. The following tumour may be associated with bladder extrophy:
Squamous cell carcinoma
Transitional cell carcinoma
Rhabdomyosarcoma
Adenocarcinoma
15
Leimyosarcoma
80. The incidence of bladder extrophy is up to:
1 in 150,000
1 in 100,000
1 in 70,000
1 in 50,000
1 in 5,000
81. The treatment for a patent urachus is:
Excision of the patent urachus and adjoining cuff of bladder
Excision of a cuff of bladder
Fulguration of the urachal tract
Partial cystectomy
Fulguration of the urachal tract and dome of the bladder
82. The commonest infecting organism in acute bacterial cystitis is:
P. mirabilis
Staphylococcus
E. coli
Pseudomonas
Klebsiella
83. The following are features of interstitial cystitis:
Commoner in females than males
Occurs mostly in middle aged women
It is accompanied by urinary infection
Characterized by irritable bladder symptoms and pain
Symptoms are short‐lived
16
84. The best method for diagnosing interstitial cystitisis:
IVU
Urethral dilatation
Cystoscopy and biopsy
Micturating cystourethrogram
CT scan
85. The best treatment for pain relief in interstitial cystitis:
Cystolysis
Ileo‐cystoplasty
Urinary diversion
Cystodiathermy of Hunner’s ulcer
Sympathectomy
86. Characteristics of vesical schistosomiasis include:
Large bladder capacity
Haemorrhgic cystitis
Initial haematuria
Bilharzial tubercles
Squamous metaplasia
87. The ideal urine sample for demonstrating eggs of S. haematobium is:
24 hr urine
12 hr urine
Early morning urine
Mid‐day urine
Voided urine any time of day
88. The following is most commonly associated with urinary Schistosomiasis:
17
Transitional cell carcinoma
Rhabdomyosarcoma
Squamous cell carcinoma
Spindle cell sarcoma
Adenocarcinoma
89. Complications of Bladder diverticulum include:
UTI
Calculus
Tumour
Bladder outlet obstruction
Ureterocele
90. The following are risk factors for developing bladder cancer:
Exposure to aniline dyes
Cigarette smoking
Alcohol drinking
Vesical schistosomiasis
High dietary fat
91. The following is associated with increased incidence of bladder cancer:
Bleomycin
Cisplatinum
Cyclophosphamide
Vincristine
Actinomycin D
92. The following are risk factors for development of bladder cancer:
Alcohol/Drinking
18
Cigarette smoking
Schistosomiasis
Irradiation
Aniline dyes
93. Adenocarcinoma of the bladder may result from the following:
Cystitis glandularis
Bladder extrophy
Urachal remnant
Misplaced prostatic glands
Squamous metaplasia
94. The risk of transitional cell carcinoma (TCC) of the bladder after earlier
development of TCC of the renal pelvis:
< 5%
5‐ 10%
10 – 20%
20 – 30%
> 40%
95. Most common cancer of the urinary bladder is:
Adenocarcinoma
Rhabdomyosarcoma
Transitional cell carcinoma
Leimyosarcoma
Squamous cell carcinoma
96. Presenting symptoms of bladder cancer:
Weight loss
19
Necroturia
Strangury
Frequency
Initial Haematuria
97. Most essential diagnostic investigation for bladder cancer:
CT scan
Patient symptoms
Intravenous urogram
Cystoscopy and biopsy
Urine cytology
98. The following are useful for the staging of bladder cancer:
Cystoscopy
Urine cytology
CT Scan
Bimanual examination
Abdominopelvic Ultrasonography
99. As a guide to prognosis and therapy, the following is the most important
distinction between levels of invasiveness of urothelial tumour:
Between epithelium and lamina propria
Between superficial and deep lamina propria
Between lamina propria and muscle layer
Between superficial and deep muscle layers
Between muscle layer and perivesical fat
20
100. Bladder cancer Invasion into superficial muscle corresponds to this stage:
T1
T2a
T2b
T3a
T3b
101. Diagnostic finding on an IVU, suggestive of bladder cancer is:
Non‐visualization of the kidney
Filling defect in bladder
Hydro‐uretero‐nephrosis
Significant residual urine
Bladder diverticulum
102. Carcinoma in situ of the bladder has the following characteristics:
Cystoscopic presence of tumour
Positive urine cytology
Irritative bladder symptoms
Best diagnosed by multiple bladder biopsies
Cystectomy is always the treatment of choice
103. Treatment for Ta and T1 bladder cancer includes:
Radiotherapy
TUR
Intravesical chemotherapy
Cystodiathermy
Cystectomy
104. Indications for intravesical chemotherapy for bladder cancer include:
21
Non‐muscle invasive transitional cell carcinoma
Single/large tumour
Multiple tumours
High grade tumours
Rapid tumour recurrence
105. Treatment of choice for a well differentiated carcinoma in situ of the bladder
Is:
Partial cystectomy
Total cystectomy
Transurethral resection
Intravesical BCG therapy
Radiotherapy
106. Leading causes of vesicovaginal fistula in developing countries include:
Irradiation
Obstructed labour
Gynaecological surgery
Malignancy
Trauma
107. Investigations for the evaluation of vesicovaginal fistula:
Micturating cystourethrogram
EUA
Dye test
Urethrocystostocopy
IVU
22
108. Characteristics of chronic urinary retention include:
Painless bladder distension
Dribbling micturation
Overflow incontinence
Commonly results from a neuropathy
Bladder volume is similar to that of acute retention
109. The length of the adult male urethra is:
10.5 cm
15.5 cm
20.5 cm
25.5 cm
30.5 cm
110. The incidence of male epispadias is:
1 in 55,000
1 in 75,000
1 in 95,000
1 in 115.000
1 in 135,000
111. Urinary incontinence from epispadias has the following features:
Occurs in the penile type
Occurs in the complete type
It is stress incontinence
It is total incontinence
Treatment requires bladder neck reconstruction
112. The following type of hypospadias may present with ambiguous genitalia:
23
Penoscrotal
Perineal
Penile
Subcoronal
Glandular
113. The estimated incidence of hypospadias is:
1 in 100
1 in 200
1 in 300
1 in 400
1 in 500
114. The following anomalies may be associated with hypospadias:
Imperforate anus
Undescended testis
Myelomeningocele
Inguinal hernia
Ambiguous genitalia
115. Technique for the repair of glandular hypospadias:
Parameatal based flap
Transverse preputial skin flap
Tranverse distal penile skin flap
Inner preputial skin flap
Meatal advancement and glanuloplasty
116. Diagnostic investigsations for posterior urethral valves:
24
Urethroscopy
Retrograde urethrogram
Ultrasonography
CT scan
Micturating cystourethrogram
117. Treatment of choice for posterior urethral valves:
Continuous bladder catheterization
Suprapubic cystostomy
Vesicostomy
Endoscopic valve ablation
Open excision of valves
118. Average incubation period for gonococcal infections:
1 – 2 days
3 – 4 days
5 – 6 days
7 ‐ 8 days
9 – 10 days
119. Features of gonococcal urethritis in the male include:
Profuse purulent discharge
Scanty watery discharge
Dysuria
Thickened and tender urethra
Normal external urethral meatus
120. Complications of gonococcal urithritis include:
25
Reiter’s syndrome
Urethral stricture
Prostatitis
Urethral cancer
Pelvic inflammatory disease
121. Characteristics of genital ulcers of lymphogranuloma venereum include:
Small and round
Painful
Usually multiple
Sloping edges
Yellowish floor
122. Extravasated urine from anterior urethral injury is bounded initially by the
following structures:
Dartos fascia
Camper’s fascia
Colles’ fascia
Bucks fascia
Scarpa’s fascia
123. Traumatic rupture of the bulbous urethra is associated with the following:
May result from a straddle injury
Produces superficial extravasation of urine
Produces deep extravasation of urine
Produces urethral bleeding
Digital rectal examination shows a high riding prostate
26
124. Investigations for diagnosing urethral stricture include:
Uroflowmetry
Ultrasonography
Retrograde urethrogram
Urethroscopy
Micturating cystourethrogram
125. Common techniques for treating urethral strictures include:
Internal Urethrotomy
Dilatation
Urethral stent implantation
One‐stage urethroplasty
Two‐stage urethroplasty
126. Aetiological factors for cancer of the penis include:
Leukoplakia
Granuloma inguinale
Phimosis
Chancroid
Balanitis xerotica obliterans
127. Penile cancer occurs most frequently at the following sites:
Glans
Meatus
Prepuce
Coronal sulcus
Shaft
27
128. T2 penile cancer has the following level of invation:
Invasion of subepithelial connective tissue
Invasion of urethra or prostate
Invasion of the corpora
Invasion of the scrotum
Invasion of the testis
129. Commonest site for metastasis from carcinoma of the penis is:
Lung
Lymph node
Liver
Bone
Brain
130. The following are prognostic factors for cancer of the penis:
Site of the tumour
Grade of the tumour
Presence of inguinal metastasis
Age of the patient
Stage of the tumour
131. Common aetiological factors of priapism:
Leukaemia
Thrombocythaemia
Pharmacologically induced
Trauma
Sickle cell disease
132. Success rate (retained potency) after treatment of major priapism:
28
< 10%
10 – 20%
20 – 30%
30 ‐40%
40 ‐50%
133. Treatment for a small T1 preputial cancer with no lymphadenopathy in a
young man is:
Radiotherapy
Circumcision
Electrocautery
Partial penectomy
Total penectomy
134. The origin of penile inervation include:
Genito‐femoral nerve
T10 – L2 spinal segments
The dorsal nerve
The cavernous nerve
S2 – S4 spinal segments
135. The action of nitric oxide within the penile smooth muscle cell involves:
Activation of adenyl cyclase and elevation of cyclic AMP level
Activation of phosphodiesterase type 4
Opening of calcium channels
Activation of guanylyl cyclase and elevation of cyclic GMP level
Closure of potassium channels
29
136. Venous flow reduction during normal penile erection is due to:
Active constriction of the superficial and deep dorsal veins
Compression of the subtunical venules and emissary veins
Active contraction of emissary veins
Opening of penile arteriovenous shunts
Relaxation of the ischiocavernous muscle
137. Normal penile erection involves the following processes:
Arterial dilatation and venous constriction
Relaxation of the ischiocavernous muscle
Arterial dilatation, venous compression and sinusoidal relaxation
Contraction of the cavernous smooth muscle
Filling and expansion of the sinusoidal spaces
138. Best treatment for low‐flow priapism that presents within 12hours of onset
is:
Aspiration of the corpora
Intravenous fluids plus analgesics
Application of cold packs
Surgical shunt
139. Post‐radical prostatectomy Impotence is often due to injury to:
Dorsal nerve of the penis
Cavernous nerve
Genitofemoral nerve
Sympathetic ganglion
30
Ilioinguinal nerve
140. Fluid and electrolyte imbalance in ureterosigmoidostomy is characterized by:
Hyperkalaemia with hyperchloraemia
Hypokalaemia with hyperchloraemia
Hypomagnesaemia with acidodis
Hyperkalaemia with hypochloraemia
Hyperkalaemia with acidosis
141. Cancer occurring in urinary intestinal diversion is most likely to occur in:
Ileal conduit
Colonic conduit
Augmentation cystoplasty
Ureterosigmoidostomy
Orthotopic neo‐bladder
Answers
D
A, D
A, C, E
A, B
D
A, B, C, D
C
B
A, D
B, C
A, C, E
A, B, C, D
B, C
D, E
C, D
A, C, D, E
B, E
31
B, D
A, D
E
B, C, E
C
B
A, C
C, D
C, D
A, E
A, C, E
D
B, D
B, C
A, D
B
D
A
A, C, D, E
D
A, B, C
D
A
D
A, B, D
A, B, C, D
A, B, C, D
A, B, D
D
B, C
B, E
A, C
A, B, D, E
A, D
C, D
D
B, C
A, D, E
B, C, D
C,
C
C
A
A, C, D
D, E
A, B
B, C
32
C, D, E
B, E
C, D
D, E
A, D, E
B, D
A, B, C, D
A, B, C
A, C, E
A, D
B, C, E
C, E
33
130. B, C, E 140. B, C
131. C, E 141. D
132. E
133. B
134. B, C, D, E
135. D
136. B
34
CHAPTER 48
SCROTUM, TESTIS AND EPIDIDYMIS
Extravasated urine from ruptured urethral bulb gravitates into the:
Scrotum
Penis
Femoral triangle
Perineum
Lower anterior abdominal wall
In the anatomy of the testis and epididymis the:
Lymphatics drain into the inguinal and para‐oartic lymph nodes
Testicular veins drain into the inferior vena cava
Nerve supply is from the sympathetic with a connection at T12
Epididymis and testis may be completely invested with tunica vaginalis
Epididymis may be anterior to the testis
Essential for sperm metabolism and motility is:
Glucose
Cholesterol
Acid phosphatase
Fructose
Ascorbic acid
Prostatic secretion is rich in:
Lactate dehydrogenase
Alkaline Phosphatase
Fibrinolysin
Folic acid
Calcium
In the physioilogy of the male generative organs:
The seminal vesicles secrete an acid viscous fluid
A large part of the semen is formed by the epididymis
The interstitial cells secrete androgens principally testosterone
The cells of sertoli probably secrete androgens
The testes are under the influence of pituitary FSH and interstitial cell
stimulating hormone
The incidence of imperfect descent of the testis is:
About 30% in premature infants
About 5% in full‐term infants
1
In about 47% of patients on the left side
In about 30% of patients on the right side
In 20% of patients bilateral
In undescended testis:
The testis is normal at birth
Retardation of its development begins at 5 years
Retardation of its development is probably due to an inherent defect and
not to the temperature of the inguinal canal
The interstitial cells atrophy if retardation of development occurs
The cells of Sertoli are never affected
An ectopic testis:
Is normal but will not develop unless it is brought into the scrotum long
before puberty
Has come out of the superficial inguinal ring
Is deflected from the normal path of descent by stenosis at the neck of
the scrotum
Lies most commonly in the femoral region
Is commoner than undescended testis
A retractile testis:
Is a testis that is held up at the superficial inguinal ring and has not
descended into the scrotum
Is retracted by contraction of an active cremaster muscle
Enters the scrotum spontaneously
Clinically can be ‘milked’ into the scrotum
Is associated with an abnormal scrotum
In unilateral undescended testis:
The scrotum looks almost like a triangle with the apex pointed upwards
The patient is usually obese
The penis is small for the age
A solid swelling is usually palpable in the inguinal canal
Attacks of pain in the groin may be the presenting symptom
Inundescended testis:
If it is bilateral, about 63% of those who have prepubertal orchdopexy
become sterile
Abou t 30% are sterile or subfertile if it is unilateral
The quantity of semen is of normal volume if it is unilateral
The sperm count is about half the normal average in most patients with
unilateral descent
2
If bilateral, 10% of patients are fertile
The complications of maldescended testis include:
Inguinal hernia
Hydrocele of the cord
Torsion
Recurrent infection
Malignancy
In the operative treatment of undescended testis:
Orchidopexy is performed ideally between 8 and 10 years to achieve
fertility
Pre‐operative androgen therapy is beneficial
If the undescent is bilateral, one side is done first and the other six
months later
Herniotomy is nearly always required
Post‐operative complications include atrophy
In maldescent presenting after puberty:
Orchidectomy is performed in unilateral undescent
Orchidopexy is done on one side and orchidectomy on the other in
bilateral undescent
Orchidectomy is done in unilateral ectopic testis
Chorionic gonadotropin therapy is beneficial
Follow‐up throughout life must always be done irrespective of the type
In idiopathic gangrene of the scrotum:
3
The whole thickness of the scrotum, nearly always the anterior surface,
sloughs off
The testes are exposed and may at times be affected by the gangrenous
process
There is usually an associated difficulty with micturition
The patient is usually quite ill
Suprapubic cystostomy leads to rapid recovery
Acute epididymo‐orchitis may follows:
Prostatectomy
Urethral instrumentation
Urinary tract infection
Reflux of urine
Excessive sexual intercourse
Organisms causing acute epidid ymo‐orchitis include:
Esch. Coli
Strep. Viridians
S. Haematobium
B. proteus
Bacteroides
In acute epididymo‐orchitis:
There is always a history of urethritis
The groin may be painful
The epididymis is swollen and very tender
Elevating the scrotum worsens the pain
There is always an associated hydrocele
The antibiotic to us in acute epididymo‐orchitis before the sensitivity of the
causative organism is known as:
Ampicillin
Chloramphenicol
Erythromycin
Amikacin
Ciprofloxacin
4
Prostatitis
Tuberculous epididymo‐orchitis:
Is usually blood‐borne
Affects the body of the epididymis before the tail
May be associated with frequency of micturition
May present as anterior scrotal sinus
Is often associated with a palpable indurated seminal vesicle
Investigations in s uspected tuberculous epididymo‐orchitis include:
Culture of early morning specimen of urine
Exretion urography
Cystoscopy
Sputum culture
Biopsy
Torsion of the spermatic cord:
Is caused by trauma to the testis
Is usually in a clockwise direction in the right testis and anti‐clockwise in
the left
May have five to ten turns
If unrelieved in 6 h may lead to gangrene and atrophy of the testis but not
usually of the interstitial cells
Is always intra‐vaginal
Torsion of the spermatic cord:
Is seen from the neonatal period to about 40 years
Occurs mainly between the neonatal period and one year and 10‐=15 y
ears
Is treated by orchidectomy if at operation the viability of the testis is
doubtful
Is treated by fixation of the testis to the dartos muscle if the testis at
operation is viable
Does not require exploration of the other testis at operation.
The clinical features of torsion of the spermatic cord include:
Sudden onset of agonizing pain in the scrotum and groin which may be
referred to the iliac fossa
Vomiting in half the patients
Frequency and dysuria
Swollen, firm, very tender and retracted test is
Lessening of pain when the testis is elevated
5
In the prognosis of torsion of the spermatic cord:
If exploration is done within 4 h the salvage rate is 100%
If exploration is done at 10 h the salvage rate is about 50%
If exploration is done after 24 h the salvage rate is almost nil
About 70% of apparently viable testes atrophy
Only about 5% of apparently viable testes have a normal sperm count.
A congenital hydrocele:
Is collection of fluid in a processus vaginalis
Is seen in all age groups
Is smaller or empty in the morning
Is distended by the end of the day
May be associated with a direct inguinal hernia
An infantile hydrocele:
Is collection of fluid in a processus vaginalis a segment of which is
obliterated
Causes a cystic swelling in the inguinal canal
Is usually seen in infants and occasionally in adults
May be associated with an indirect inguinal hernia
May disappear spontaneously
Primary vaginal hydrocele:
Occurs in all age groups especially those between 10 and 20 years
Results from deficient drainage of fluid in the tunica vaginalis by the
lymphatic vessels which may be blocked or hypoplastic
Always has a thin sac
Is not always unilocular
May contain calcareous deposits on its wall
The fluid in primary vaginal hydrocele:
Has a specific gravity of 1.022 to 1.025
Is brown in colour
Contains cholesterol and albumin
Contains sodium chloride, carbonates and fibrinogen
Collects rapidly
The fluid in secondary vaginal hydrocele:
Collects slowly
Is always serous or blood‐stained
Is commonly an exadate from inflamed tunica vaginalis
May be considerable, up to 500ml
Contains uric acid
6
Secondary vaginal hydrocele may be associated with:
Acute or tuberculous epididymo‐orchitis
Filariasis
Torsion of the spermatic cord
Testicular tumours
Lymphoedema of the scrotum
Complications of primary vaginal hydrocele include:
Infection
Atrophy of the testis
Calculus formation
Impotence
Haematocele
A primary vaginal hydrocele in a 30‐year old man may be treated by:
Hydrocelectomy
Tapping
Lord’s operation
Hydrocele‐orchidectomy
Jaboulay’s operation
A cyst of the epididymis is:
A retention cyst of the seminiferous tubules
Lobular and may be up to 10cm in diameter
Above and behind the testis
Usually multi‐locular and the surface is bosselated
Left alone if it is small and aspirated if it is large
Varicocele is:
Dilatation, elongation and tortuosity of the spermatic vein
On the right side in about 90% of patients
Seen commonly in young unmarried men
Best felt with the patient lying down
Treated by ligation and division of the spermatic vein at the internal ring
7
if there is persistent pain or subfertility
In a patient with a varicocele the:
Sperm count is depressed
Percentage of motile sperms is depressed
Volume of the semen is depressed
Percentage of immature sperms is depressed
Fructose concentration of the semen is depressed
Testicular tumours
Account for about 1% of tumours in Causasian males
Are more commonly encountered in Africans
In about 10% arise in undescended testes
Are all radio sensitive
Are most commonly seminomas
In the pathology of testicular tumours:
Seminoma is fast‐growing and the cell resembles a spermatocyte
Seminoma is firm and grayish or creamy in colour and usually
homogenous
Teratoma may be slow, or fast‐growing and originates in a primitive
pluripotent cell
Teratoma has a honeycombed cystic appearance and is usually yellow in
colour
Teratoma is seen between 40 and 50
Of the teratomas of the testis:
Malignant teratoma undifferentiated (MTU) is the most malignant
Teratoma differentiated (TD) behaves like a benign tumour
Malignant teratoma intermediate (MTI) has a combination of
differentiated and undifferentiated teratoma
Malignant teratoma trophoblastic (MTT) and malignant teratoma
anaplastic (MTA) produce chorionic gonadotrophins
Malignant teratoma trophoblastic spreads rapidly by the blood stream to
the lungs and liver when the tumour is small
Testicular tumours usually metastasize to the following lymph nodes:
Inguinal
External iliac
Para‐aortic
Mediastinal
Supraclavicular
8
Teticular tumours present most commonly as :
Secondary vaginal hydrocele
Enlarged painless or heavy testes
Acute pain simulating acute epididymo‐orchitis
Hepatomegaly
Respiratory problem
Gynaecomastia, loss of libido and aspermia may be due to:
Malignant teratoma intermediate
Seminoma
Lymphoma
Interstitial cell tumour
Sertoli cell tumour
Sexual precocity and herculean muscular development in a boy of 10years
may be due to:
Interstitial cell tumour
Sertoli cell tumour
Seminoma
Malignant teratoma trophoblastic
Teratoma differentiated
Measures taken in the treatment of testicular tumours include:
Orchidectomy through the scrotum
Pre‐operative radiotherapy of the testis
Radiotherapy of the para‐aortic and ipsilateral pelvic nodes
Post‐operative cystotoxic therapy whether or not there are metastases
Biopsy, cytotoxic chemotherapy, and surgery for residual masses in
advanced malignant teratoma
Cytotoxic drugs used in the treatment of malignant teratoma include:
Vinblastine and bleomycin
Bleomycin and Etoposide
Cis‐Platinum
Etoposide
9
Markers used in the management of testicular tumours include:
Serum alkaline phosphatase
Serum human chorionic gonadotrophin
Carcino‐embryonic antigen
Serum uric acid
Alfa‐fetoprotein
A 3‐month old baby has a soft, fluctuant swelling extending from the right
hemiscrotum to the internal ring. According to the mother, it is small in the
morning and get bigger by the end of the day.
The most likely clinical diagnosis is:
Complete, right, indirect, reducible inguinal hernia
Right vaginal hydrocele plus right, indirect, incomplete reducible inguinal
hernia
Irreducible complete right indirect inguinal hernia
Congenital hydrocele
Infantile hydrocele
10
Vaginal hydrocele
57. Incidence of undescended testis in full‐term babies examined at birth is:
1.4%
2.4%
3.4%
4.4%
5.4%
58. Most common location of the ectopic testis is:
Perineum
Femoral
Suprapubic
Contralateral scrotum
Superficial inguinal pouch
59. The incidence of cryptorchidism at one year of age is:
3.8%
2.8%
1%
0.8%
O.1%
60. Factors that may influence testicular descent include:
11
Scrotum
Gubernaculum
Temperture
Obstructing fibrous bands
Hormonal imbalance
61. Best time after birth for children with undescended testis to undergo
surgery is:
Within 12 months
12 – 18 months
18 – 24 months
24 – 30 moths
30 – 36 months
62. The following may predispose to Fournier’s gangrene:
Perianal sepsis
Urethral stricture
Periurethral abscess
Testicular torsion
Diabetes mellitus
63. The following are true of Fournier’s gangrene:
It is a form of necrotizing fasciitis
May occur in previously healthy individuals
The disease affects the testes
It can affect both adults and children
It is caused by opportunistic and synergistic organisms
64. The following are implicated in Fournier’s gangrene:
12
Enterococci
Microaerophilic Streptococcus
Bacteroides
Fusobacterium
Clostridium
65. Complications resulting from acute epididymo‐orchitis include:
Abscess formation
Testicular atrophy
Development of chronic pain
Infertility
Chronic epididymo‐orchitis
66. Torsion of the testis is generally common in the following age group:
5 – 10 years
10 – 15 years
15 – 20 years
20 –255 years
25 – 30years
67. The following may predispose to testicular torsion:
Horizontal inversion
Hydatid of Morgagni
Long narrow mesorchium
Chronic epididymitis
High investment of tunica
68. The following are true of testicular torsion:
It is most common around puberty
13
It does not occur in neonates
It must be differentiated from epididymo‐orchitis
Watchful waiting is the preferred treatment
On the right the direction of torsion is clockwise
69. Irreversible ischaemic injury of the testis becomes pronounced after
the following duration of torsion:
1 hr
2 hrs
4 hrs
6 hrs
8 hrs
70. The following swelling may fluctuate in the course of the day:
Infantile hydrocele
Congenital hydrocele
Vaginal hydrocele
Encysted hydrocele of the cord
Epididymal cyst
71. The most likely cause of testicular injury from varicocele is:
Elevated scrotal temperature
Testicular hypoxia
Effect of adrenal metabolites
Altered levels of spermatic vein testosterone
Testicular hypertension
72. Germ cell tumours constitute the following percentage of all testicular
Malignancies:
< 80%
14
80 – 85%
85 – 90%
90 – 95%
> 95%
73. Testicular tumours constitute the following percentage of male
cancers
1%
2%
3%
4%
5%
74. The undescended testis accounts for the following percentage of
testicular tumours:
4%
6%
8%
10%
12%
75. The commonest testicular tumour of infancy and childhood is:
Seminoma
Yolk sac tumour
Adenomatoid tumour
Choriocarcinoma
Lymphoma
15
76. The following are germ cell tumours:
Yolk sac
Seminoma
Choriocarcinoma
Leydic cell tumour
Teratocarcinoma
77. Commonest presentation of a germ cell tumour of the testis in a young
adult man is:
Testicular pain
Testicular swelling
Reactive hydrocele
Bilateral gynaecomastia
Chronic cough with haemoptysis
78. Concerning tumour markers used in testicular cancer management:
Serum alpha‐ fetoprotein (AFP) elevation do not occur in pure
seminoma
Syncytiotrophoblastic cells are responsible for the production
of beta‐human chorionic gonadotrophin (HCG)
AFP originates in cells from the yolk sac
Approximately 5 – 10% of seminoma patients have raised HCG
79. Alpha‐fetoprotein is produced by the following testicular tumours:
Yolk sac
Seminoma
Teratocarcinoma
16
Embryonal carcinoma
Choriocarcinoma
80. The following are routine investigations in a case of testicular
Cancer:
Tumour markers
Lymphangiogram
Histopathology of affected testis
Bone scan
Chest X’ray
81. Testicular tumour markers are indicated for the following:
Staging testicular tumours
Determine malignant potential of the tumour
Determine best treatment option
Monitor response to treatment
Detect relapse after treatment
82. Alpha fetoprotein is raised in the following:
Teratoma
Choriocarcinoma
Pregnancy
Pure seminoma
Primary hepatoma
83. The most radiosensitive testicular tumour is:
Choriocarcinoma
Seminoma
Embryonal cell carcinoma
17
Yolk sac tumour
Teratocarcinoma
84. Preferred treatment option for Stage 1 seminoma after orchidectomy
is:
Surveillance
Chemotherapy
Retroperitoneal lymph node dissection
Combination of chemotherapy and radiotherapy
Radiotherapy to para‐aortic and ipsilateral pelvic nodes
85. Preferred treatment for Stage 1 teratoma after orchidectomy is:
Surveillance
Chemotherapy
Radiotherapy
Retroperitoneal lymph node dissection
Combination of chemotherapy and radiotherapy
86. Treatment of choice for metastatic testicular teratoma is:
Actinomycin D , Methotrexate and Chlorambucil
Cisplatinum, Methotrexate and Bleomycin
Bleomycin, Etoposice and Cisplatinum
Vinblastin, Bleomycin and 5‐Fluorouracil
Cisplatinum, vinblastin and 5‐Fluorouracil
87. Modified retroperitoneal lymph node dissection preserves fertility in
most patients by sparing the following structure:
Genitofemoral nerve
Internal iliac artery
18
Seminal vesicles
Postganglionic sympathetic nerve fibers
Pelvic parasympathetic plexus
88. Optimum treatment for patients with advanced seminoma after
orchidectomy is:
Radiation
Immunotherapy
Retroperitoneal lymph node dissection
Radiation plus chemotherapy
Chemotherapy
89. The 5 – year survival rate for Stage I seminoma is:
70%
75%
80%
85%
90%
90. In non‐seminomatous germ cell tumours, the following factors
determine the risk of metastatic disease:
Presence of teratoma
T‐stage
Presence of embryonal cell carcinoma elements
Vascular invasion
Lymphatic invation
Answers
A, B, C, D, E
19
D, E
D
A, C, E
C, E
A, E
A, E
B
B, C, D
E
A, D
A, C, E
C, D E
B, D
A
A, D, E
A, D
A, B, C, D
A, D
A, B, C, D
A, B, D
B, C
E
D
C, E
A, B, C
B, D
B, D
A, C, D
C, D, E
B, D, E
A, C, D
C
A, B, D, E
A, B, C, E
B, D
A, C
C
C
A, B
A, C, E
B, C, D
B, C, E
C, D, E
20
B
E
A
A, B, C, D
C, E
A, B, C, D
B, E
D
C
B
E
A
57. C 83. B
58. E 84. E
59. D 85. A
60. B, D, E 86 C
61. A 87. D
62. A, B, C, D 88. E
63. A, B, D, E 89. E
64. B, C, D, E 90. B, C, D, E
65. A, B, C, D, E
66. B
67. A, C, E
68. A, C, E
69. C
70. B
71. A
72. D
73. A
74. D
75. B
76. D
77. B
78. A, B, C, D
79. A, C, D
80. A, C, E
81. A, D, E
82. A, C, E
21
CHAPTER 6
CUTANEOUS ULCERS, SINUSES, FISTULAE
1
Chronic osteomyelitis of the underlying bone
Tetanus
Lymphoedema of the foot
Malignant change in the ulcer
Rifampicin
Clofazimine
Streptomycin
Co-trimoxazole
INAH
An ulcer of yaws:
May start as a granulomatous papule
Has sloping edges
Has dirty yellowish sloughing floor
May heal spontaneously, the skin over it becoming depigmented
2
Does not cause enlargement of regional lymph nodes
An ulcer:
A non-specific ulcer:
In the acute phase is painful and has a sloughing floor covered with
purulent discharge and a sharp edge with oedematous tender
surrounding skin
In the transition phase has a sloping edge and grayish-yellow floor.
In the reparative or healing phase is painless and pink granulation
fills the floor
In the chronic phase has grayish floor with a thin odourless
discharge
The fifth phase is malignant change
In an indolent or callous ulcer, the:
Base is indurated
Floor has pink granulation tissue
Edges are rigid and hard
Surrounding skin is warm and oedematous
Epthelium at the edge grows inwards
Complications of non-specific ulcers of the lower leg include:
Chronic osteomyelitis
Amyloidosis
Below knee lymphoedema
Deformities of the foot or ankle
Venous thrombosis
A painful circular ulcer with sloping edges on the dorsum of the
foot near the big toe in a 60-year old man could be due to:
Leprosy
Varicose veins
3
Arterial disease
Malignant melanoma
An abscess
The prime cause of a venous ulcer following deep venous
thrombosis is:
Varicosity of the long saphenous vein
Venous stasis
Back pressure in the veins
Destruction of the valves of the perforating and deep veins
High venous pressure in the legs
A venous ulcer usually:
Is situated just above the medial malleolus
Is irregularly circular
Has a deep floor with pink granulation
Has punched out edges
Has indurated base
4
Haemoglobinopathic ulcer:
Is most often found in the lower limb close to the lateral malleolus
Is associated with atrophic skin and hyperpigmentation
Heals quickly
Often breaks down again after healing
Bed nest worsens it
Haemoglobinopathic ulcer is difficult to treat because of:
Lowered oxygen tension
Recurrent haemolytic crisis
Fibrosis around the ulcer
Low haemoglobin level
Lack of appropriate personnel
A 50-year old man has a 0.5cm ulcer on the nose which has a
raised and rolled up edge. It is of 2/12 duration.
A sinus:
Connects two epithelial surfaces
May be congenital
Has a discharge which is always present
Is treated with antibiotics
Unresolved infection may cause acquired sinus.
Causes of a sinus include:
Chronic ulcer
Achnonycosis
Amyloidosis
Buruli ulcer
Foreign body e.g. Sutures
In the treatment of a sinus:
Excision of sinus is indicated in congenital type
Dressing alone adequate for acquired type
5
Tract of the sinus may be laid open and dressed
In tuberculous, sinus treatment of TB lesion leads to healing
Penicillin exhibition contributes to healing
Causes of acquired fistula include:
Abscess that ruptures into a cavity and skin
Burns
Granulomatous lesions
Benign tumours
Schistosoma haematobium
The following are examples of neoplastic ulcers:
Squamous cell carcinoma
Renal cell carcinoma
Kaposi sarcoma
Malignant melanoma
Dermato fibrosarcoma Protuberans
Diabetic Ulcer:
Ulcers in a patient with Diabetes Mellitus
May be caused by infection
May be caused by trauma
May be caused by pressure necrosis
Basis in hypoaesthesia from blood loss
6
May be associated with tuberculous bone infection
In Buruli ulcer differential diagnosis of the pre ulcerative form
include:
Onchocercoma nodule
Lipoma
Sebacous cyst
Naevus
Phyconycosis
Complications of Buruli ulcer include:
Anaemia
Contracture
Proximal lymphoedena
Marjolin’s ulcer
Osteitis
In the treatment of Buruli ulcers the following practitioners are
involved:
Physiotherapist
General Surgeon
Orthopedic Surgeon
Opthalmologist
Maxilloficial Surgeon
CHAPTER 6
CUTANEOUS ULCERS, SINUSES, FISTULAE
ANSWER
A
A, C
7
C, D
A, B, C
A, B, C
B, C, D, E
B
B
A, B, D
A, C
C, D
C, D
A, C
A, C
C, D
C, E
D
A, B
B
A, B, E
A
B, D
A, B, C, D
E
B
B, E
A, C, D
A, C
A, B, C, D
A, B, C, D
D, E
A, C, E
A, C, E
A, B, D
A, C
8
CHAPTER 14
BURNS
A Burn:
Is coagulative destruction of skin which may be caused by hot water
Occurs most commonly in children
Is pathologically different from scald
Injury depends on the temperature of the heat source but not on the
duration of exposure of the tissues to such temperature
In the adult may be due to RTA
In deep partial thickness burns destruction of the following occur:
Lymph vessels
The hair follicles and sebaceous glands
Sweat glands
Red cells
Capillaries
Mediators released after burns include:
Histamine
Cyclo-oxygenase pathway products
Serotonin
Prostaglandins
Thyroxine
Cold water immersion after thermal injury:
Increases the risk of infection
Reduces pain after partial thickness burns
Can result in hypothermia if applied to large burns
Has been reported to stabilize mast cells
May decrease oedema if applied immediately
The protein content of oedema fluid in burns may be as much as
(g/1):
60
20
30
40
50
The electrolyte composition of oedema fluid in burns:
Has a higher sodium concentration than plasma
Has a lower potassium concentration than plasma
Has a higher bicarbonate concentration than plasma
1
Has a lower chloride concentration than plasma
Is the same as that of plasma
In burns:
The maximum oedema fluid obtainable is about 10% of body
weight or 50% of total E.C.F
There is initial vasodilatation followed by vasoconstriction
The rate of fluid exudation from the capillaries is highest in the first
6h. and falls in 48h.
Increased capillary permeability may occur even in unburnt areas
Immediate charring of the skin lessens external and subcutaneous
fluid loss
Anaemia in burns may be caused by:
Thrombosis
Increased red cell fragility
Changes of dressings
Bone marrow depression
Skin grafting
In burns:
There is depression of cellular and immunological mechanisms
Leucocytes cannot phagocytose bacteria normally
There is depression of lysosomes
IgG is not affected
Transfer of leucocytes and antibodies to sites of bacterial infection
is rapid and not depressed
In burns:
Renal failure is commonly caused by toxic substances produced in
the burnt skin
The urine may occasionally be port-wine
Uraemia is always associated with oliguria
There may be necrosis of the distal convoluted tubules
The renal vessels are dilated
Organisms that may infect a burn in the first 24h include:
Proteus
Streptococcus
Pseudomonas
2
Esch. Coli
Staphylococcus
Predominant organisms in a scald wound by seven days include:
Staphylococcus
Pseudomonas
Pneumococcus
Clostridium tetani
Streptococcus
3
Face
Neck
Entire trunk
Perineum
Axilla
Curling’s ulcer:
Occurs only in the stomach and duodenum
Occurs only in severe burns
Is often complicated by bleeding
May be prevented by the administration of antacids or cimetidine to
severely burnt patients in the first three weeks
Is best treated by partial gastrectomy or vagotomy and drainage
4
burns
of the face, right upper limb and anterior part of the trunk
following a fire
in is bedroom at 12 midnight. He is brought to the ‘Casuality’ at
2.00 a.m.
Your first concern will be to:
Check his pulse and blood pressure and administer morphine.
Remove his clothes and determine the extent and depth of his burn
Check the rate of his breathing
Find out if the airway is clear
See if there is singeing of his nasal hair or soot in the nostril
Examination of the burnt area shows that there are blisters, areas
of erythema and other areas of skin which are all sensitive to pin
prick.
The burn is:
Superficial partial thickness
Deep partial thickness
Full thickness and superficial partial thickness
Partial thickness (superficial and deep)
Full thickness
The burn is estimated at 30% of his body surface. The total fluid
requirement (in litres) in the first 24h is about:
5.5
6
6.5
7.2
7.5
The fluids will consist of:
2L 5 per cent dextrose, IL blood and the rest as Ringer’s lactate
Ringer’s lactate
5
2L blood and the rest as ringer’s lactate
2L 5 per cent dextrose and the rest as Ringer’s lactate
IL 5 per cent dextrose; 2L dextran 70 and the rest as Ringer’s
lactate
Half the fluids should be given by:
6a.m
8a.m
10a.m
12noon
2p.m
Initial investigations will include:
Haematocrit
Blood group
Serum electrolytes and blood urea
Culture of the burnt skin
White cell count and differential
The antibiotic to administer at this stage is:
Chloramphenicol
Cloxacillin or penicillin
Gentamicin
Oxytetracycline
Cephaloridine
The most important parameter to monitor is:
Quarter-hourly pulse and blood pressure
Central venous pressure
Filling of peripheral veins
Hourly urinary output
Skin temperature and orientation
After cleaning the burn wounds with one per cent centrimide you
will apply:
Terracortril spray daily
0.5% silver nitrate dressing and add more silver nitrate every 3h
6
Silver sulphadiazine cream on alternate days without dressing
Mafenide creame twice daily
Povidone-iodine daily
The fluid requirement (in litres) in the second day is
approximately:
4
4.5
5
5.5
6
On the second day the urine is found to be port-wine in colour.
You will after examining the urine:
Restrict fluid intake
Order an urgent I.V.P.
Give blood
Give 10% mannitol
Give sodium bicarbonate
On the 8th day he complains of some pain in the wound, anorexia
and generally being unwell. His temperature is 38.50C and the skin
around the discharging wound looks reddened.
The clinical diagnosis is:
Cellulitis
Lymphangitis
Septicaemia
Burn wound sepsis
Necrosis of the burn
Effects of electrical injuries include:
Cardiac or respiratory arrest
Ventricular fibrillation
Auricular fibrillation
Rupture of blood vessels
Thrombosis of vessels
Late complications of electrical burn injuries include:
Impotence
Cataract
Epilepsy
Intractable headache
Abnormal gait
7
In electrical injuries:
8
102
103
104
105
106
9
Inflammable liquids should not be stored in the home
Epileptics should be banned from getting near fires
In electrical burn:
Extent of injury may be difficult to assess
In the presence of myoglobinuria IV lasix in indicated
Infusion of IV fluids must be at the rate to increase urine output to
above
50 mls/hr
Excision of necrotic muscles is indicated 48hrs after diagnosis
Silver sulphadiazine is contraindicated in this type of burn.
10
CHAPTER 14
BURNS
ANSWER
B, E 35. A, B, C, D, E
A, B 36. B, D, E
A, B, C, D 37. B
B, C, D, E 38. D
E 39. A, B, D, E
E 40. A, C, E
A, D 41. D
A, B, C, D, E 42. C, D
A, C 43. C, D, E
B, D 44. A, C, D, E
B, E 45. B, C, E
B 46. B, C, E
A, B, E 47. A, C
A, E 48. A, B, C, D
A, C 49. A, C, D, E
A, E 50. C, D
11
A, B, D
C, D
C
B, C, E
A, B, C, D, E
D
D
C
D
B
A, B, C
B
D
C
E
D, E
D
A, B, D, E
12
CHAPTER 16
Keloid:
Keloid:
Excision
1
None of the above
A sebaceous cyst:
Dermoid cyst:
A ganglion:
Is usually unilocular
2
Is best treated by aspiration of its contents and injection of
hydrocortisone sclerosant
Varruca vulgaris:
A 25-year old man has two swellings over the right greater trochanter.
The swellings are firm, mobile, circumscribed, non-tender,
subcutaneous and attached to the deep fascia.
Fibromata
Lipomata
Implanatation dermoids
Onchocercomata
Naevi(moles)
3
Should be excised as they may become malignant.
Bleeding
Ulceration
Hairiness
Increase in size
Increase in pigmentation
Desmoid tumour:
Haemangiomas:
4
The treatment of cavernous haemangioma at the age of five is:
Leave alone
Excision
Injectionof a sclerosant
Neurofibroma:
Lipoma:
5
and neck region in Caucasians
5-Fluouracil
Methotrexate
Cyclophosphamide
Cisplatin
Bleomycin
6
Occurs in the face in 90% of patients
Malignant melanoma:
Vincristine
7
Melphalan
Adriamycin
Actionmycin D
Dacarbazine
Dermatofirosarcoma:
Kaposi’s sarcoma:
8
Is most common in Jews, Italians and Africans and the highest
incidence in Africa is in Uganda
Bones
Intestines
Brain
Lungs
Liver
9
May be localized or generalized
Pathological fractures
Sclerosis
Osteoporosis
Cystic changes
Surgery
Radiotherapy
Chemotherapy
Paclitaxel
Chlorambucil
Doxorubicin
Vincristine
Etoposide
10
Fibrosarcoma:
Rhabdomyosarcoma:
A hypertrophic scar
Is treated by excision
A rich vasculature
11
Low mesenchymal density
Malignant melanoma
Freckles
Concerning melanoma
12
trunk and grows slowly
<1mm
1-1.5mm
1.5-2mm
2.1-4mm
>4mm
In non-whites
Genital sites
In stable diabetics
Rhabdomyosarcoma
13
Hepatic metastases occur very early
Rhabdomyosarcoma
Liposcraoma
Prognosis is poor
14
May present a jigger
Nodular
Fungating
Fleshy
Plaques
Visceral
15
In soft tissue sarcomas
Nodular
Subcutaneous
In subungual melanoma
16
The following are important in the assessment of melanoma
Tumour thickness
Presence of ulceration
Host response
Chest Xray
Serum LDH
Bowan’s Disease
17
Is 2-3 times more common in woman
Burno
Varicose vein
Pressure sore
Lonizing radiation
Chronic ulcers
Neurofibromatosis
Lymphangioma
18
hygroma
Answers
C
C, D
E
A, C
B, C, D
A
B, C
E
A, B
A, B, D, E
C, D
B, C, E
A
B, D
E
B, D
A, E
B, D, E
19
B
A, D
C, E
B, E
A, B, E
B, C,D
A, C
A, B, C, D, E
B, E
B
C, D, E
D, E
A, C, D, E
A, B
C, E
A, B, D
A, C, D
A, B, D, E
A, B, C, D
A, B, D
C, D, E
B
B, C, E
A, B, D
20
A, C, D
C, D, E
B, C, D
A, D, E
A, D, E
A, C, D, E
A, B, D
B, C, D
A, C, D, E
A, B, C, D
C, D, E
B, D, E
A. B, E
B, E
A, C, D
21
CHAPTER 18
PLASTIC SURGERY
Autograft
Isograft
Heterograft
Xenograft
Homograft
Isograft
Allograft
Homograft
Heterograft
glands
Grows hair
Shrinks considerably
1
Full thickness graft:
Shrinks considerably
Grafts:
A graft will die unless the blood supply from the recipient site to
the graft is developed within:
1 day
1-2 days
2-3 days
4 days
5 days
2
There is close approximation of the graft to the recipient site
Methods that can be used to cover a recipient site when the graft
is inadequate include:
Mesh graft
Sheet graft
Pinch graft
At the usual storage temperature keeps the graft viable for 4 weeks
In bone grafting:
3
Banked bone is as good as living bone
Too much hammering and chiseling may kill off the osteoblasts and
undifferentiated cells of the bone marrow
Ribs
Femur
Tibia
Iliac crest
Skull
Cartilae graft:
4
Forms epidermoid cysts
A flap:
Must have the end attached to a new position left for one week to
pick up new blood supply before the other end is detached
Ear
5
Heart
Kidney
Limb
Liver
The graft vesels become more dilated and the graft oedematous
from
Disruption of the vessel wall with haemorrhage into the graft occurs
in the body
system
in size
6
The anomaly of cleft palate and cleft lip:
Is commoner in females
cleft lip:
Vit. C deficiency
Rubella
Toxoplasmosis
Syphilis
Nitrogen mustard
Heredity
Vit. A deficiency
Vit. B deficiency
Irradiation
7
Unknown
3 processes
4 processes
5 processes
6 processes
7 processes
Nose
Nostrils
Nasal septum
Upper lip
Premaxilla
Cheeks
8
Philtrum
Upper jaw
Nasal septum
9
If it extends into the nostril splitting the alveolus, then is complete
If it is incomplete, is only a minor lip notch and does not involve the
whole lip
If incomplete, the fissure affect only the uvula or the uvula and soft
palate
Breast-feeding
Cup-feeding
Spoon-feeding
10
The main aim of surgery in cleft palate (secondary palate) and
Cosmetic
Facilitate feeding
1-6
6-12
12-18
18-24
24-30
4-8
8-12
12-16
16-20
20-24
11
Langer’s lines are skin lines of maximal tension that run parallel to
skin creases
Langer’s lines are seen more easily on the faces of older persons
Cartilage
Bone
Fat
Nerve
Muscle
12
In free tissue transfer there is successful anastomosis of vessels in
the flap to vessel at the recipient site
Groin flap
Axillary flap
Fasciocutaneous flap
Bone flap
Muscle flap
In tissue expansion:
dome flap
The silicone is then removed at the end of inflation and skin utilized
as a flap
Feeding
Cosmetic
Hearing
Airway
13
Speech
The aim is to produce a long mobile palate that will close the
oronasal sphincter
In breast reduction:
Pressure sores:
14
Ischial areas and occipital may be affected
Fibrin seal
Plasmic imbibitions
Inosculation
Revascularization
Clot fixation
Movement
Innervation
Lymphatic drainage
Blood supply
Tissue content
Trauma
Vascular malformations
15
Abnormal scarring
Skin cancers
Main problems with the child born with cleft palate deformity only:
Appearance
Feeding
Failure to thrive
Bipedal oedema
Speech deformity
Bone graft
Use of prosthesis
Secondary surgery
Counselling
Speech therapy
Reduction mammoplasty
Angrecitation mammoplasty
Reconstruction of breasts
Mytidectomy
Genioplasty
16
Repair to palate carried out before normal speech develops
One parent and or child affected the probability of next child is 15%
Ear reconstruction:
17
Elevation of framenoration and skin graft done:
CHAPTER 18
PLASTIC SURGERY
ANSWERS
18
E 30. B
B, C, D 31. B
B, D 32. B
A, C, D 33. C, D, E
B, E 34. A, B, C, D
C 35. A, D, E
E 36. A, C, E
A, B, D, E 37. B, D, E
A 38. B
C, D 39. A, C, E
C, D 40. A, B, D
C 41. A, B, C, E
B, E 42.B, C, D
A, B, C, E 43. A, D, E
A, E 44. A, B, C, D, E
A, C, D 45. B, C, E
B, D 46. A, B, C, D, E
B, C, E 47. A, B, D, E
A, C 48. A
B, C, E 49. A, B, D, E
E 50. A, E
A 51. A, C, D
C
19
A, B, C, E
A, C, E
C, E
B, C
B, D
A, C, E
20
CHAPTER 19
MONTH, TONGUE AND SALIVARY GLANDS
Part or the whole of the following structures may be lost in cancrum oris:
Mandible or maxilla
Lips
Palate
Nose
Eye
1
Measures taken in the treatment of the EARLY stage of cancrum oris
include:
Intravenous fluids
High protein high calorie diet and vitamins
Sequestrectomy
Administration of penicillin
Nasogastric decompression
A ranula:
Occurs in the floor of the mouth usually in the midline
Is a transparent white or bluish cyst
Contains clear serous fluid
Is commonly seen in young adults
Is excised or marsupialized
2
Leukoplakia is probably caused by:
Syphilis
Tobacco chewing
Herpes febrilis
Spirits
Ill-fitting dentures
3
Is typically sited in the mid-posterior tongue
Has punched out edges
Has a regular outline
Often heals spontaneously
4
Wide local excision
Partial glossectomy
Subtotal glossectomy
Partial glossectomy plus block dissection of the ipsilateral cervical lymph
nodes
Subtotal glossectomy plus block dissection of the ipsilateral lymph nodes.
5
superficial and deep lobes
The entry of the facial nerve is about 2.5cm below the external auditory
meatus in the direction of the tip of the nose.
The duct opens into the mouth opposite the site of the upper second
premolar tooth
Tumours and inflammation cause a uniform enlargement of the gland
The gland extends from the zygomatic arch to the angle of the mandible.
Saliva:
Contains ptyalin which hydrolyses starch to glucose
Aids speech
Prevents buccal infection
Secreted by the parotid gland is mucous
Secreted by the submandibular gland is serous and mucous
Salivary secretion:
Is about 2L/day
By the submandibular gland is about 1L/day
Has a pH of about 7.0
At the normal pH is saturated with calcium
Is effected by sympathetic stimulation of the salivary glands.
Salivary calculus
Is ten times commoner in the submandibular gland than in the parotid
although the parotid section contains a higher concentration of calcium.
Consists essentially of phosphates of calcium and magnesium
May be oval or round in shape
6
Is usually single
Is radio-opaque in all patients
In Mickulicz disease:
There is usually symmetrical enlargement of the salivary and lacrimal
glands
The month is dry
Auto-immunity is probably the cause
The salivary tissue is replaced by fibrous tissue
Radiotherapy has not been found beneficial
Adenolymphoma:
Occurs in all races
7
Is often multiple and may be bilateral
Occurs predominantly in females over 40
Usually occurs at the angle of the mandible or below it
Is about 2-3cm in diameter, firm with cystic areas or entirely soft and
fluctuant
A man of 60 presents with pain in the right ear of six months duration;
two months earlier he had noticed a painless induration on the right
lateral aspect of the tongue. On examination he is a fit individual with
clean oral hygiene and a flat non ulcerating thickening of the epithelium
on the right edge of the tongue with much salivation. There are no
palpable lymph nodes.
8
Ultrasound scan of the tongue and oral carity
Retro screen of the patient
Cytology of oral washings
Wedge biopsy of the lesion.
CHAPTER 19
A, B, D
C
E
A, B, D, E
A, B, C, D, E
A,B , C
A, B, D
A, B, C, D, E
B, E
A, D, E
A, D, E
A, B, C, E
A, B, D, E
A, C, D
B, C, D, E
A, C, D
A, D, E
A, , E
A, B, C
C, E
A, C, D
E
A, B, D, E
A, C
9
A. N. C
B, D
A, B, C, E
A, B, C, D, E
A, C
C, E
A, B, E
B, C, D, E
A, D, E
A, B, E
C, D
A, B, C
C
A, B, C
B, C, D
A, C, D
E
B, D, E
C
A, B, D, E
B
B
E
B
10
CHAPTER 20
OTORHINOLARYNGOLOGY
Are three conchae or turbinates all of which are normally seen on routine examination
of the nose.
The middle meatus contains the ostia of the posterior ethmoidal cells and the
spenoidal sinuses
The inferior meatus contains the ostia of the maxillary and frontal sinuses and the
anterior ethmoidal cells.
Are present at birth but small and highly placed below the orbit.
Are related in its floor to the teeth from the incisor to the third molar
Have the floor above that of the nose at birth, level at 7 years and below that level
at full development.
Are related to the cavernous sinuses and nasopharynx and the sphenoids
Are related to the anterior cranial fossa, orbit and olfactory nerves.
Unilateral nasal discharge and occasional epistaxis in a5 – year old boy are most
1
suggestive of:
Suppurative rhinitis
Allergic rhinitis
Sinusitis
Rhinitis sicca
In epistaxis :
The bleeding in most patients is from a plexus of the capillaries in the antero-
inferior portion of the nasal septum
The blood in the nose is removed and the nose pinched for 5-10 minutes
Is very painful
Sneezing with itching of the nose ,eyes and throat ,watering of the eyes and clear
nasal discharge is most suggestive of :
Acute rhinitis
2
Allergic rhinitis
Maxillary sinusitis
Frontal sinusitis
Acute pharyngitis
Chronic rhinitis
Septal haematoma
Nasal polyp
Antibiotics
Vitamin C
Steroids
Systemic antihistaminics
3
A painless granuloma that originates in the inferior turbinate and spreads in the
sub mucosa and through the bony structures to the dorsum of the nose and the
central part of the face is most probably:
Rhino sporidosis
Nasal entomophthorosis
Aspergilloma
Aspergillosis
Mucormycosis
Nasal entomophthorosis
African histoplasmosis
Rhinosporidosis
A 50-year old man complains of a 3- month history of nasal obstruction which was at
first unilateral and is now associated with offensive discharge.
Chronic Sinusitis
Nasal polyp
Septal deviation
Foreign body
Superior constrictor
Stylopharyngeus
4
Cricopharyngeus
Middle constrictor
Palatopharyngeus
A 10 – year old boy suffers from mouth breathing, nasal obstruction ,nasal discharge
and recurrent right earache.
Maxillary sinusitis
Otitis media
Rhinitis
Recurrent tonsillitis
Influenza virus
Staphylococcus
Streptococcus
C – diphtheria
Pneumococcus
Rheumatic fever
Otitis media
Vincent’s angina
Glandular fever
A 20-year old woman has a 3-day history of severe pain on the right side of the
throat which radiates to the ear. Dysphagia is severe, trismus is present and pyrexia
5
is marked.
Right tonsillitis
Pharyngitis
Vincent’s angina
Administration of antibiotics
Acute tonsillitis
Recurrent tonsillitis
6
May cause atelectasis
A 20- year old man complains of sorethroat ,headache and fever for one week,
examination reveals redness of the throat, enlarged cervical lymph nodes ,splenomegaly
and a skin rash.
Scarlet fever
Agranulocytic angina
Diphtheria
Infectious mononucleosis
Vincent’s angina
In agranulocytic angina:
Retropharyngeal abscess:
7
If acute, is treated by incision under G. A.
A pharyngeal pouch:
Requires oesophagoscopy
May occur during the inspiratory phase only or during the inspiratory and
expiratory phases
8
Recurrent laryngeal is sensory to the areas below the vocal cords
A 4-year old girl has severe inspiratory stridor, prostration, fever and some
cyanosis for one day.
Bronchopneumonia
Acute laryngo-tracheo-bronchitis
Acute bronchitis
Pharyngeal diphtheria
C. Diphtheria
Pneumococcus
Influenza virus
Staphylococcus
Haemolytic streptococcus
9
Treatment may include:
Naso-tracheal intubation
Tracheostomy
An adenoma
Common in singers
Found at the junction of the posterior and middle thirds of each cord
A 50-year old man has persistent hoarseness for 4 weeks without any pain.
You will suspect most strongly:
Chronic laryngitis
Chronic pharyngitis
10
Has a male/female ratio of 10:1
Functional origin
Laryngomalacia
Laryngo-tracheo-bronchitis
Bifid epiglottis
Angioneurotic oedema
Expiratory stridor
Inspiratory stridor
Hoarseness of voice
11
Cyanosis
The lining of the cartilaginous portion contains hair follicles and sebaceous and
ceruminous glands
The direction in the cartilaginous part is slightly downward and backward and in
the bony part upward and forward
There is no bony portion in the infant and the tympanic membrane is almost
horizontal
Vestibule
Cochlea
Semi-circular canals
Utricle
Tympanic membrane
12
Outwards
Forwards
Backwards
Downwards
Upwards
Outwards
Forwards
Backwards
Downwards
Upwards
Deafness
Dizziness
Vestibular nystagmus
Tinnitus
Headache
13
Keratosis obturans:
May cause ulceration of the meatal lining and pressure erosion of the bone
B. Pyocyneus
Candida
Aspergillus
Monilia
Allergen
A 10-year old boy who has been having severe pulsating right earache, high
fever and headache for a week now complains of severe pain behind the right
ear.
Acute mastoiditis
14
Pus in the external meatus which collects rapidly after it has been cleaned
Cortical mastoidectomy
Myringotomy
Administration of penicillin
Cerebral abscess
Meningitis
15
The lower half of the face is paralysed
Emotional movement of the face is completely paralysed and returns more slowly
than voluntary movement
In bell’s palsy:
There is loss of taste of the anterior two – thirds of the ipsilateral side of the
tongue
Prednisolone is efficacious
A 45- year old man has an hour, of severe rotational vertigo associated with unilateral
deafness, tinnitus, headache and nausea.
Hypertension
Hypotension
Intracranial tumor
Labyrinthitis
Menier’s disease
Nicotinic acid
Vit. B complex
Vit. C
Stemetil
16
Penicillin
Advancing age
Otitis media
Meniere’s syndrome
Otosclerosis
17
A. Is common in boys
B. Is common in girls
C. Usually presents with recurrent torrential epistaxis
D. Is usually diagnosed by biopsy of the lesion from nasal cavity
E. Diagnosis is usually confirmed by angiography
18
CHAPTER 20
KEY
19
E
A, D, E
B, D
C
A, C, D, E
D
B
A, B, C, D, E
B, C, E
B, C, D
D
C
E
B
D
A, B, C, E
A, B, D
C
B, C, D
B, C, E
A, D
D
A, B, E
B, C
C, E
20
B, C
B
B, C
C
B
C, E
A, C, E
B
D
C
D
A, C, E
B
A
C, E
B
A, C, E
C, D
A, D
A, C
B, D
C
B
A, C
B, D
21
A, B, C, D, E
B, C
B, C, E
A, C E
E
A, B, D
B, D
B, E
A, B, C, E
B, D, E
B, C, E
A, C, E
22
CHAPTER 21
Bleeding
Respiratory obstruction
Shock
Infection
Aspiration of vomitus
Lateral
Thigh extended
Bronchoscopy
Tracheostomy
1
General anaesthesia is preferable to local analgesia
Occur most commonly in the angle and body in the canine/incisor regions
Splinting of the teeth on either side of the fracture is simple and effective
A sling of bandage passing under the chin and pinned firmly to a head
bandage is adequate
2
Protrusion and swelling of the cheek
Epistaxis
In the majority of cases both condyle and disc are displace posteriorly on
the articular eminence
3
There is no need for immobilization if reduction is done within 48h of
injury
Swollen
Quite painful
Red
Tender
Pregnancy
Gum recession
Malnutrition
There are small vesicles which may coalesce to produce large ulcers
4
Periapical (alveolar) abscess may follow:
Gingivitis
Trauma to a tooth
Stomatitis
Fusiformis fusiformis
Borrelia vincenti
Staph.pyogenes
Esch coli
Ludwig`s angina
Orbital cellulitis
5
sinuses
Penicillin
Chloramphenicol
Clindamycin
Teracycline
Amikacin
Gingivitis
Impacted tooth
Periapical (alveolar)abscess
Dental extraction
6
Compound or simple fracture of the jaw
A fibrous epulis:
Is common in adults
7
colour
Grows rapidly
Granuloma gravidarum:
Is hard
Is red
Is lobulated
Odontomes include:
Cyst of eruption
Ameloblastoma
Cementoma
Dentinoma
Dental cyst
A 25-year old man has a swelling of the ramus of the right mandible. The
surface is lobulated and egg shell crackling is elicited.
It may be:
Periodontal cyst
Ossifying fibroma
Ameloblastoma
Osteoclastoma
8
Odontogenic myxoma
Dentigerous cyst:
Presents as a smooth swelling with a thick outer wall usually on the labial
side of the alveolar part of the jaw
Is treated by removing the cyst lining and tooth and filling the cavity with
bone chips
Ameloblastoma:
Arises from the epithelium of the enamel and is always fast-growing and
solid
Has a lobulated surface and the overlying teeth are usually not affected
9
Microscopically ossifiying fibroma shows:
Giant cells
Osteoblasts
Proliferating fibroblasts
Area of calcification
Pathological fracture
Cervical lymphadenopathy
Dysphagia
Radiolucent swelling
10
Hemimandibulectomy
Radiotherapy
Pathological fracture
Pain
Swelling
Unerupted teeth
Osteosarcoma
Burkitt`s lymphoma
Fibrous dysplasia
Periodontal cyst
11
Dentigerous cyst
CHAPTER 21
B
A, C
B, D
B, C
D, E
A, E
A, D
C, E
A, C
B, D
A, C, D, E
A, B, D, E
B, E
A, C, E
B, D
12
A, C, D, E
C, E
A, C, D
E
A, B, D, E
C, D
B, C, E
A, B, E
A, C, D
C, D
C, E
A
A, E
B, C
B, D, E
A, C
A, B, E
D
C
D
A, B, C, E
13
CHAPTER 22
THE THYROID AND PARATHYROID GLAND
A. Isthmus lies in front of the first, second and third tracheal rings
B. Weight of the gland is 7-25 g in the African
C. “Strap muscles” consist of the sternothyroid, sterno-hyoid and the
inferior belly of the omo-hyoid
D. Medial relations of the lateral lobes are the hyoid, thyroid and cricoid
cartilages
upper six tracheal rings, oesophagus and recurrent laryngeal nerve
E. Superior and middle thyroid veins drain into the internal jugular vein
and the
Inferior thyroid veins into the innominate vein
Serum T3 concentration
T3 resin uptake
Serum T4
Serum free thyroxine
Free T4 index
Free T4 index
Serum thyroid stimulating hormone
Test of hypothalamic-pituitary axis
1
Protein bound iodine
Serum T3 concentration
5. In thyroid scan:
6. Thyroglossal cyst:
7. Goitre:
Exists when more than 10 per cent of any community have goitre
Does not occur in West Africa
2
Is caused principally by low iodine content of the local soil
Is caused by cassava containing cyanogenic glucosides in some parts
of Africa
Affects adolescent boys and girls in roughly the same ratio
Hoarseness of voice
Snoring during sleep
Difficulty in swallowing
Oedema of face and conjunctivae
Engorged manubrial subcutaneous veins
May occur at any age from the neonate to the elderly but the peak
incidence is from 21 to 30
Affects women five times more than men
Is symptomless in the vast majority of patients(apart from the
swelling)
Is multinodular involving both lobes in about 50 per cent of patients
Feels soft or firm and has indefinite edges
3
A. Is seen more commonly in endemic areas
B. May affect children
C. Is seen most commonly in girls from around puberty to 20
D. Is a uniformly enlarged and soft thyroid gland
E. Does not become big enough to compress the trachea
Tetany
Infection
Sudden haemorrhage
Malignancy
Myxoedema
X-ray of neck
Free thyroxine index
Serum T3 concentration
Direct laryngoscopy
Isotope uptake test
A. Administration of thyroxine
B. Excision
C. Lobectomy of the affected lobe
D. Administration of Lugol’s iodine
E. Subtotal thyroidectomy
Administration of thyroxine
Subtotal thyroidectomy
Administration of Lugol’s iodine
Lobectomy
Radio-iodine
19. Thyrotoxicosis:
4
If primary, is associated with a pre-existing diffuse hyperplastic
goiter
If secondary, may be associated with malignant thyroid
May be precipitated by ingestion of large doses of iodine in a patient
with long-standing goitre
Is uncommon in Africans
20. In thyrotoxicosis:
22. The following is/are found in the orbit and extraocular muscles in
exophthalmos
Erythrocytes
Plasma cells
Giant cells
Polymorphs
Reticulocytes
Constipation
Insomnia
5
Gynaecomastia
Oligomenorrhoea
Tiredness
Moist hands
Auricular fibrillation
Lid lag
Palpable thyroid
Hyperkinetic movements
26. Exophthalmos:
Conjunctival oedema
Diplopia
Corneal ulceration
Diminishing visual acuity
Directly related to the severity of hyperthyroidism
6
29. The thyroid gland in thyrotoxicosis:
Weight loss
Blood pressure
Sleeping pulse rate
Restlessness
Appetite
Primary thyrotoxicosis
Meningioma
Carotid-cavernous fistula
Optic nerve glioma
Orbital tumour
7
to tyrosine
Potassium perchlorate prevents trapping of iodine and coupling of
MIT and DIT to T2 and T4
Carbimazole prevents binding of iodine to tyrosine and coupling of
MIT and DIT to T2 and T4
Phenobarbitone relieves palpitation and excessive sweating
Diarrhoea
Arthralgia
Skin rashes
Depression
Anaemia
8
38. Radio-active iodine:
Depresses the activity of most of the thyroid cells but does not
destroy them
Is fully effective in 4 weeks
May induce carcinomaof thethyroid in the elderly
Is only given to patients over 55 years
Leads to hypothyroidism in 40-50% of the patients in 5 years
41. Propranolol:
Is an alpha-blocking agent
Controls the symptoms and signs of thyrotoxicosis because it can
depress the production of thyroxine
Is effective within 24 h of administration and the dose is80 mg orally
daily
Is usually given for 4-7 days before and 10-14 days after subtotal
thyroidectomy
Is currently preferred to the usual anti-thyroid drugs for making toxic
patients euthyroid
42. Soon after the removal of the endotracheal tube after subtotal
9
thyroidectomy
for secondary thyrotoxicosis, a patient is found to be having
severe difficulty
in breathing.
Is permanent
If unilateral causes hoarseness of voice and non-productive cough
If bilateral causes severe hoarseness of voice and difficulty in
breathing
If bilateral requires early repair of the nerves
If bilateral and there is no recovery after one year, requires
arytenoidectomy with lateral fixation of one cord
10
46. Hypoparathyroidism after subtotal thyroidectomy:
Is fairly common
Is caused by excessive release of TSH in the post-operative period
Is characterized by excitation, profuse sweating, hyperpyrexia and
and tachycardia
Is treated with propranolol, Lugol’s iodine, carbimazole, diazepam and
intravenous fluids
May require oxygen administration and cold sponging
11
Abortion
Postmature labour
Stillbirth
Eclampsia
Foetal goitre and hypothyroidism
54. Hypothyroidism:
12
or aspirin
If congenital is always associated with a goitre
In the adult is not associated with a goitre
If congenital causes mental and physical underdevelopment
sometimes
with deaf-mutism
13
A. Pain or discomfort in the thyroid area of the neck
B. Severe hyperthyroidism
C. Hypothyroidism
D. Nodular goitre
E. Solitary nodule
Is fairly common
Is seen from childhood to old age with a peak incidence in Africa
In the 4th decade
Is 3 times more common in men
May arise in a nodular goitre
May present with hypothyroidism
14
predominantly
mixed papillary and follicular carcinoma
E. Heredity is a factor in some cases of medullary carcinoma
15
67. A 35-year old woman presents with a solitary thyroid nodule which
has been
present for about 4-years, but has recently been enlarging. It is firm,
rather
circumscribed and fairly mobile. There are no enlarged cervical
lymph nodes.
A. A cyst
B. An adenoma
C. Nodular goitre
D. Papillary or follicular adenocarcinoma
E. Anaplastic carcinoma
68. If the scan shows it to be “hot” with some uptake in the rest of the
thyroid,
you will consider:
A. A cyst
B. An adenoma
C A papillary or follicular adenocarcinoma
D. Nodular goitre
E. An autonomous nodule
69. If the scan shows it to be “cold”, you will consider:
A cyst
An adenoma
A papillary or follicular carcinoma
Nodular goitre
An autonomous nodule
Horner’s syndrome
Cervical lymphadenopathy without thyroid swelling
A pulsatile skull swelling
Hyperthyroidism
Diarrhoea
16
71. Measures taken in the treatment of operable papillary or follicular
carcinoma
of the thyroid include:
Near-total thyroidectomy
Irradiation
Radio-active iodine
Cytotoxic therapy with adriamycin or bleomycin
Administration of thyroxine
Near-total thyroidectomy
Irradiation
Radio-iodine
Cytotoxic therapy with bleomycin and adriamycin
Administration of thyroxine
84% and 60% of those with papillary carcinoma are alive at 5 and 30
years
60% and 40% of those with follicular carcinoma are alive at 5 and 30
years
No patient with anaplastic carcinoma is alive at 3 years
Those over 40 have a better prognosis than those under 40
Women have a better prognosis than men
Palpitations
Profuse sweating
Progressive weight loss inspire of polyphagia
Consistent heat intolerance
Diarrhoea
17
Moist hands
Atrial fibrillation
A sleeping Pulse Rate > 120/min
A sleeping Pulse Rate > 90/min
Pretibital mxyoedema
18
Benign solitary nodule
Hashinoto’s thyroiditis
Lymphadenoid goitre
Papillary carcinoma of the thyroid
Medullary carcinoma of the thyroid
19
Convulsions
Stridor and dyspnoea
Excessive sweating
Pyrexia
Restlessness
85. Late complications of hypoparathyroidism include:
88. Hyperparathyroidism:
Is an uncommon disease
Is more common in men
May be seen at any age
May be symptomless
May precipitate acute pancreatitis
20
Anorexia
Nausea and vomiting
Muscle cramps
Numbness around the lips, polyuria and polydipsia
Restlessness
Sclerotic skull
Subperiosteal resorption of bone seen particularly in the
middle phalanges of the index and middle fingers, upper part
of the tibia and neck of the femur
Nephrocalcinosis
Periosteal thickening of the radius and ulna
Calcification of the spleen
92. In hyperparathyroidism:
21
Excessive intake of antacids
Multiple myelomatosis
Sarcoidosis
Osteitis deformans
Multiple bone metastases
Severe weakness
Abdominal cramps
Copious vomiting
Irritability
Drowsiness
22
CHAPTER 22
THE THYROID AND PARATHYROID GLAND
ANSWERS
A, B, E
A, B, D
D
B
C
D, E
D, E
B, C, D, E
A, C, D, E
B, D, E
A, B, C, D, E
A, B, C, D, E
C
A, B, C, D
C, D
23
A
C
A, B, C
C, D
B, E
B, D, E
B
B, C, D, E
A, C
A, B, D, E
A, D
A, B, C, D
B, C, D
B
B, D
C, E
A, B, C, D, E
D
A, C, D
A
24
B, C, E
C
E
A, E
A, C, D
C
D
C, D, E
A
B, E
B, E
C, E
A
A, B, D
A, C
A, D
A, C
C, D
B, E
A, C, D
25
A, C
A, D
A, C, D
B, D
B, C
B, D
A, E
A, B, D
A, D, E
A, C, E
A
B
B, E
A, B, C, D
A, B, D, E
A, C
B, D
A, B, E
D
D
26
B, E
A
B
E
C
D
C, D, E
A, D, E
A, B
B, C, E
C, D
C, E
A, C, D, E
A, B, D, E
E
B, C
A, C, D
B, C, E
A, C, D, E
C, D, E
27
B
28
SURGERY
CHAPTER 23
THE NECK
A. Epiglotis
B. Common carotid artery
C. External jugular vein
D. Internal jugular vein
E. Brachial plexus
A. Horner’s syndrome
Aerial fistula
C. Dysphonia
1
D. Mediastinitis
E. Surgical emphysema
Ludwig’s angina:
A branchial cyst:
A branchial fistula:
2
pit
C. Usually presents around puberty
D. Opens at the junction of the middle and lower thirds of the anterior
border of
the sternomastoid
A cystic hygroma:
Occurs in the posterior triangle of the lower third of the neck, axilla
or cheek
Chemodectoma:
A. Lymph node
B. Lipoma
C. Sternomastoid tumour
D. Aberrant thyroid
3
E. Neurofibroma
A. Thyroglossal cyst
B. Dermoid cyst
C. Brancial cyst
D. Sebaceous cyst
E. Ranula
A 25 year old man has a 3 month old, painless swelling below the
angle of the mandible. It is tense, fluctuant mobile, and most
deep to the sternomastoid
A. Chronic abscess
B. Pharyngeal diverticulum
C. Lipoma
D. Branchial cyst
E. Laryngocele
A. Metastases
B. Hodgkin’s lymphoma
C. Tuberculosis
D. Sarcoidosis
4
E. Multiple neurofibromatosis
A. Larynx
B. Right lung
C. Stomach
D. Pancreas
E. Right breast
A. Chemodectoma
B. Lymph node
C. Parotid tumour
D. Submandibular salivary gland tumour
E. Lipoma
In Ludwig’s angina:
5
C. Excessive salivation and trismus are presenting symptoms
D. Broad spectrum antibiotics such as cefuroxime and metronidazole
should be
Administered
E. The tongue is oedematous and is displaced upwards and forwards
6
B. The ESR may be normal
C. Screening for HIV is not essential
D. The Mantoux test, unlike in pulmonary tuberculosis, is usually
unremarkable
E. Excision biopsy may be necessary to establish the diagnosis
Branchial cyst:
Brancial fistula:
A. Arises from failure of the second branchial arch to fuse with the fifth
arch
B. Arises from failure of the first branchial arch to fuse with the fourth
arch
C. Has abundant lymphoid tissue in the wall
D. Should be excised through 2 or 3 small transverse incisions over the
course
of the tract
E. Is lined by columnar and ciliated epithelium in its inner portion and
stratified
squamous in its outer portion
Cystic hygroma:
7
C. Is best treated by sclerotherapy as this has been found to be very
effective
D. Is completely compressible
E. Has a 90% chance of recurrence following excision
8
9
CHAPTER 23
THE NECK
ANSWERS
A, C, D
E
B, C, D, E
C, E
A, E
C, D, E
B, C, E
A, D
C
B
D
A
A, B, C
B, C
A
A, B, C, D
C, D, E
10
A, E
A, B, C
A, C, D, E
A, B
B, C
11
CHAPTER 59
OPHTHALMOLOGY
1
Optic nerve compression may be indicated by red colour desaturation
Diplopia is common in axial proptosis
Photopsia is common in cases caused by primary optic nerve tumours
Ocular surface lubricants have no effect on visual disturbance
Is always reversible
2
Levator palpabral superioris muscle
Reflex stimulation of the zygomatic branch of the Facial Nerve
The presence of the Muller muscle which is enervated by the
sympathetic nerve
15. Blepharitis
Is always an infective condition
Is often associated with dry eyes
Treatment include shampooing of the lid margin
When chronic may lead to loss of eyelashes
May require prolonged antibiotic treatment
16. A stye
Is inflammation of the of the Meibomian glands
Is often caused by Staphylococcal infection
Is usually painless
Is best treated by local application of steroid eye ointment
May be drained by epilation
17. Chalazion
Is a granuloma of the Meibomian glands
Is rarely multiple in the same eyelid
Is a swelling that is fixed to skin
The underlying tarsal conjunctiva is usually normal
Is treated by incision and curettage
18. In trichiasis
The eyelid margin is turned inwards
Causes include keratitis
Symptoms of foreign body sensation in the eye are surprisingly rare
There may be an extra row of eyelashes more posterior than usual
Epilation often provides a cure
3
19. In ectropion
The lid margin loses its normal opposition to the globe
The cause may be lid laxity
The normal wetting of the cornea is affected
Watering eyes is often a frequent complain
Treatment is not necessary as it is self limiting
20. Lagophthalmos
Is inability to open the eye completely
May be caused by injury to the Facial nerve
May lead to glaucoma
Is often seen in proptosis
Is treated by padding the eye with sterile gauze.
21. The cornea
Is a major refractive component of the eye
Has stratified squamous epithelium
Is transparent mainly because of the arrangement of the collagen fibres
in its stroma
Is vascularised in disease processes
Requires healthy precorneal tear film for its function
4
Is rarely super infected by bacteria
May sometimes require weak steroid eye drops for treatment
Are effectively treated by Acyclovir ointment
5
Topical antibiotics are essential for treatment
33. Trachoma
Is a keratoconjunctivitis
Rarely causes blindness
May be eradicated without antibiotics
Is caused by a chlamydial organism
Blindness is due to corneal scarring
Trachoma
Vernal conjunctivitis
Siderosis Bulbi
Ochronosis
Onchocerciasis
36. Pinguecula
Is found in the interpolpebral conjunctiva on either side of the cornea
Occurs in the young
Is a degenerative lesion
May affect visual acuity
Is treated by excision
37. Pteyigium
Is an avascular thickening of the conjunctiva encroaching on the
cornea
Is most common in the tropics and sub tropical regions of the world
Is most common after 60 years
Does not affect vision
Needs excision with conjunctival autografting
6
May present as a painless sector redness of the eye
Usually disappears within 2 weeks
May complicate whooping cough
Needs to be drained sometimes
May be found in someone with a fracture of the base of the skull
44. The following are known causes of secondary open angle glaucoma
Conjunctivitis
Corneal ulcer
Steroids
Pigment dispersion in the anterior chamber
7
Trauma
8
Topical steroids
Padding of the eye
Topical antibiotics
53. Cataract
Occurs more frequently in old age than from trauma
May occur more frequently some families than others
May sometimes be associated with narrowing of the anterior chamber
Is always associated with poor vision
Can be prevented sometimes by the appropriate immunization
57. Aphakia
9
May result from couching
May result in distance vision becoming poorer than near vision
May be associated with deep anterior chamber
Causes the pupil to become jet black
is best treated with intraocular lens implantation
10
Retinal tears
Retinal exudates
Retinal venous occlusion
11
Ask the patient to see the Ophthalmologist as soon as soon as they
notice any visual loss
Laser treatment for any exudates in the retina
Regular eye examination by an ophthalmologist
Topical treatment o retinopathy using steroids
Pan retinal laser photocoagulation for new vessels on the disc
74. Retinoblastoma
Is the commonest tumour of the retina in childhood
Occurs most commonly after age 5 years
Is always unilateral
In the early form presents with pain and redness of the eye
Is almost invariably fatal
12
Excessive use of accommodation in high hypermetropia
Congenital myopia
Loss of vision in the eye before age 4 years
Enophthalmos
77. Detection of various forms of strabismus
Alternate cover test detects alternating strabismus
Latent strabismus is detected by eliminating simultaneous perception
Intermittent strabismus is diagnosed from the history
In esotropia, the corneal light reflex is displaced nasally
In pseudo strabismus, the corneal light reflex is central
79. The following may indicate the presence of optic nerve disease
Red colour desaturation
Reduced light brightness sensitivity
The presence of relative afferent papillary defect
Near vision more affected than distance vision
New vessels on the optic disc
13
Chapter 59 Answers
A 43. C,D
C 44. C,D,E
A, B, C, E 45. A,C,D
A, C 46. A,B,C
D 47. B,C,E
A 48. A,D,E
C, D, E 49. A,C,D
C 50. A,B,C,D,E
A, B, E 51. A,C
A, C 52. A,C,D
B, E 53. A,B,C,E
A,B,C,D,E 55. E
A, E 59. A,C,E
D 60. A,B,C,E
14
B 62. A, C,D
A 66. A,D
E 72. A,B,D
A,C,D,E 74. A
B 77. B,C,E
A,B,C,D,E
A,B,C,D
B,E
A,B,C,D,E
15
CHAPTER 53
1
Allows early mobilization of muscles and joints thereby preventing
wasing of muscles and stiffness of joints
Reducses the incidence of deep venous thrombosis
Promotes early healing of the fracture
Should be delayed until other life threatening injuries have been treated
2
year old man
becomes confused, dyspnoeic and has a low-grade fever. Some
petechial rashes are observed. You will suspect most strongly:
A. Lobar pneumonia
Septicaemia
Pulmonary embolism
Fat embolism
Cerebrovascular accident
A. Antibiotics
Oxygen
Heparin
Sedation
To be left alone
Callus
Delayed union
Union
Non-union
Avascular necrosis
13. Fracture of the clavicle:
Occurs most commonly in the middle third and usually as a result of
direct violence
If in the middle third, the medical fragment is pulled upward and
backward and the lateral fragment downward and forward
Causes the patient to tilt his head to the contralateral side
Is best treated with a “figure-of-eight” bandage which is re-applied
every other day and retained for six weeks
Is commonly complicated by non-unions and mal-unions.
14. Fractures of the scapula:
Are caused by direct violence
Are usually associated with fractures of the underlying ribs
3
Seldom cause severe displacement of the fragments
Are best treated by the use of a sling for 3 weeks followed by active
mobilization exercises.
The best treatment is open reduction and internal fixation with plates
and screws
15. Acromio-clavicular joint dislocations:
Is commonly caused by a fall or blow on the tip of the shoulder
Is common among horse riders and car drivers
Causes downward displacement of the clavicle and upward
displacement of the acromion
X-rays should be taken with the patient standing
Is best treated by the use of a sling even when displacement is
considerable.
16. The shoulder joint is:
Held together by a strong but thin capsular ligament which is lax
superiorly
Strengthened anteriorly by the subscapularis tendon
Strengthened inferiorly by the infraspinatus tendon
Strengthened superiorly by the supraspinatus tendon
Weakest in the superior aspect
4
18. The most likely clinical diagnosis is:
Acromio-clavicular dislocation
Posterior dislocation of the shoulder
Fracture of the surgical neck of the humerus
Anterior dislocation of the shoulder
Fracture of posterior half of the head of the humerus
19. The lesion which is commonly associated with this injury is damage
to the:
Median nerve
Ulnar nerve
Radial nerve
Axillary nerve
Brachial artery
20. Complications of anterior dislocation of the head of the humerus
include:
Injury of the axillary artery
Injury to the supraspinatus and other rotator cuff muscle
Fractures of the greater tuberosity
Recurrent dislocations of the shoulder
Injury to the pectoralis major
21. The pathological findings in recurrent dislocations of the shoulder
include
Tear of the supraspinatus
Postero-lateral notch in the humeral head
Detachment of the glenoid labrum and capsule from the scapular neck
Anterior pouch of the capsule under the coracoid process
Laxity of the infraspinatus muscle
5
The arm is then adducted sweeping the elbow across the body to the
midline
The arm is then internally rotated so that the hand falls near the
opposite shoulder
A collar and cuff sling is then applied
23. The Bankart’s operation is used for:
Luxatio erecta
Posterior dislocation of the shoulder
Fracture dislocation of the shoulder
Fracture of the tuberosity of the humerus
Recurrent dislocation of the shoulder
24. In a tear of the supraspinatus tendon, the typical feature is:
Tenderness over the shoulder
Stiffness of the shoulder
Inability to initiate abduction, but when abduction is passively initiated
the patient is able to continue
Inability to adduct the shoulder
Palpable defect in the supraspinatus tendon
25. In the treatment of fractures of the surgical neck of the humerus
If the fracture is impacted, the arm is put in a sling and daily active
assisted movements started
If the fracture is impacted and the displacement is minimal, the arm is
put in a plaster-of- Paris U-slab and strapped to the body for 3 weeks
after which active assisted movements are started
If displacement is severe, manipulation is done and the arm held in
plaster-of-Paris shoulder Spica for 6 weeks.
If there is associated dislocation of the head, open reduction is often
necessary
If the axillary nerve is injured, exploration and open reduction are
urgent
26. If a patient suspected of having fracture of the shaft of the right
humerus is
unable to extend the wrist and fingers, you will:
6
27. A child of 6 after falling on the outstretched hands has a painful
tender swelling
of the right elbow. You will:
Do a check x-ray
Examine the hand for swelling
Check the radial pulse
Check the brachial pulse
Check for any neurological lesion
31. In a supracondylar fracture:
7
The lower fragment in 90% of patients is displaced backwards and
upwards and may be rotated medially
The brachial artery may uncommonly be injured and requires treatment
within 6 hours of the injury
Stiffness of the elbow is common and is treated by forced extension,
passive movements and active exercises
Mal-union is common and usually requires open reduction
The median nerve is commonly injured
8
Fracture of the olecranon process
Dislocation of the elbow
Monteggia fracture dislocation
Fracture of the head of the radius
36. In dislocation of the elbow:
The cause is usually direct violence to the elbow
The radius and ulna are displaced forward in relation to the condyles of
the humerus
The line from the medial epicondyle through the tip of the olecranon to
the lateral epicondyle is straight
A back slab is applied for 6 weeks after reduction
Recurrence may be due to associated fracture of the coronoid process
9
Madelung’s deformity
Fracture of the radial styloid
Fracture of the scaphoid
Smith’s fracture
Monteggia fracture
41. In a Colles’ fracture:
The wrist is immobilized in palmar flexion and ulnar deviation after
reduction
An above elbow plaster is usually applied especially if the fracture is
comminuted
Immobilization is usually for 3-4 weeks
Complications include reflex sympathetic dystrophy, shoulder-hand
syndrome, rupture of the extensor pollicis longus tendon and
Volkmann’s ischaemic contracture of the fore-arm
Is most common in middle-aged men
42. In Smith’s fracture:
There is a fracture of the distal end of the radius
The distal fragment is displaced posteriorly
There is anterior rotation of the distal fragment
The cause is a pronation injury produced on falling on the flexed wrist
After reduction, an above elbow plaster is applied with the wrist in full
supination and slight dorsiflexion
10
Usually treated by closed manipulation and open reduction being
necessary
only occasionally
If accompanied by fracture of the head of the radius in a child is treated
by excision of the head of the radius and intramedullary nailing of the
ulna
45. A Galleazzi fracture is:
Fracture of the radius with dislocation of the proximal radio-ulnar joint
Produced by a blow on the forearm
Treated by open reduction and plating
Treated by closed manipulation
Mobilized by a below-elbow plaster
46. Fractures of the scaphoid:
Is produced by a direct blow on the carpus
Typically causes pain and tenderness in the anatomical snuff box
Is not always evident on x-ray
May be complicated by avascular necrosis and osteoarthritis
Is immobilized in a below-elbow plaster with the thumb in full internal
rotation
and the plaster extended to the metacarpo-phalangeal joint
47. Kienbock’s disease:
Is an insidious avascular necrosis of the scaphoid
May be associated with trauma
Causes paraesthesia of the hand
Is usually seen in young adults
Is usually seen in children
11
maintain
May necessitate arthrodesis
49. A rolled bandage held in the palm of the hand and held by a crepe
bandage is
used to immobilize:
12
52. In mallet finger:
The terminal phalanx is held in flexion deformity
The terminal phalanx cannot be flexed
The flexor tendon avulses a portion of the terminal phalanx at its
insertion
The finger is immobilized in a splint with the proximal interphalangeal
joint
flexed and the distal interphalangeal joint hyperextended for 3 weeks
If a large portion is avulsed then operative excision is necessary
53. A patient is suspected of having a fracture of the scaphoid. X-ray is
negative.
You will:
13
of the symphysis
A 30-year old woman in the front seat of a car injures her right hip
following an accident involving the car. The right leg is shortened,
internally rotated, flexed and adducted.
14
Rupture of the femoral artery
Myositis ossificans
Fracture of the anterior lip of the acetabulum
15
Intertrochanteric fracture
Anterior dislocation of the hip
66. Non-union of fracture of the neck of the femur in an elderly woman is
BEST
treated by:
Full hip spica
Hemi-arthroplasty
Dynamic hip screw
MacMurray’s osteotomy
Insertion of a bone graft
16
Arthrodesis of the hip
A car knocks down a 30-year old man. He complains of severe pain in
the left thigh and is unable to raise the leg. Examination reveals
deformity and swelling of the thigh with flexion, abduction and
external rotation of the proximal part of the thigh.
70. The fracture of the femur is at the:
Greater tuberosity
Upper third
Middle third
Lower third
Supracondyles
71. Which of the following may occur?
Injury to the popliteal artery
Injury to the femoral artery
Injury to the popliteal nerves
Injury to the sciatic nerve
Shock
72. Indications for internal fixation of a fracture of the shaft of the femur
include:
Old or frail patients
Patients between 5 and 12
Patients with multiple injuries to the lower limb
Pathological fractures from metastasis
Angulation of the fractured fragments
73. A Gallow’s splint is used in children for treating fracture of the:
Tibia and fibula
Supracondylar region of the femur
Shaft of the femur
Neck of femur
Anterior dislocation of the hip
74. A 25-year old man is suspected of having a supracondylar fracture of
the right
17
femur. You will:
77. Which of the following disabilities of the knee may occur after
excision of the
patella?
18
78. Which of the following muscles maintain the knee in the extended
position
during walking?
Popliteus
Rectus femoris
Vastus medialis
Gracilis
Vastus lateralis
79. Which of the following is/are true of the ligaments of the knee?
The lateral collateral ligament is more commonly ruptured than the
medial collateral ligament
In rupture of the medial collateral ligament the knee is unstable
on adduction
Medial collateral ligament rupture is usually treated by applying a knee
brace for 6 weeks
The anterior cruciate ligament is ruptured by an extension force driving
the tibia forwards relative to the femur
Anterior cruciate ligament rupture is treated by surgical reconstruction
80. Which of the following is/are true of tears of the menisci?
As the medial meniscus is attached to the medial collateral ligament, it
is less commonly torn than the lateral meniscus
They occur if the semi-flexed knee is twisted while weight-bearing
In the bucket handle tear, the commonest, the tear extends into both
horns
and the fragment is displaced inwards
They cause haemarthrosis
They may heal spontaneously
81. Clinical features of acute tears of the medial meniscus include:
Inability of the patient to straighten the knee fully after injury to the knee
Swelling of the knee
Wasting of the quadriceps muscle
Attempted passive extension of the knee causes pain in the whole
knee
Appley’s grinding test is positive
82. Which of the following is/are true of fracture of the lateral condyle of
19
the tibia?
It is less common than that of the medial condyle
Oblique shearing fractures should always be treated conservatively
A comminuted compression fracture is treated by Hamilton Russell skin
traction and knee exercises
Depressed plateau fracture is treated by open reduction in the young
It may lead to genu varum
83. Which of the following is/are true of fractures of the tibia and fibula?
Fracture of the tibia is always accompanied by the fracture of the fibula
Oblique fractures are unstable and tend to shorten and displace in
plaster
even when the initial reduction is good
Shortening may be overcome by skeletal traction using a Steinman’s
pin
through the calcaneum
The full-length leg plaster extends from the mid-thigh to the metatarsal
heads
with the knee slightly flexed at about 10o and the ankle at 90o
It is not essential to examine the leg for circulatory impairment when
the patient
is first seen as pressure on blood vessels and nerves is caused by
tight
dressing or plaster cast
84. Indications for open reduction and internal fixation in fractures of the
tibia and
fibula include:
20
Anterior marginal fracture of the lower end of the tibia with anterior shift
of the talus
Avulsion fracture of the medial malleolus with spiral fracture of lateral
malleolus
Isolated shearing fracture of the medial malleolus
Shearing fracture of the medial malleolus with transverse fracture of
the lateral malleolus
Lower tibia
Pelvis
Lower thoracic spine
Lumbar spine
Basi-occiput
89. A 30-year old farmer is carrying a heavy load on her trips and the
load falls
backwards from the head. She may sustain:
21
Cord injury without radiological evidence of vertebral injury is indicative
of extension-rotation injury
Wedge compression fracture occurs in pure extension injury and is
stable
Wedge compression fracture is commonest in the thoracic region
Contusion on the forehead suggests an extension injury
Fracture dislocation at T12-L1 is stable
91. In paraplegia following spinal injury:
Normal bladder function usually returns after 3 months
Diarrhoea often occurs
Violent flexor and adductor spasm of the paralyzed limbs may occur
Spirit applied daily to the skin prevents pressure sores
There should be daily passive movements of all paralyzed joints and
the unaffected upper limb muscles
A 7year old boy is rushed into the emergency room with a swollen,
painful
and deformed left elbow. He had fallen off from his school desk
about 3 hours
ago.
22
A twenty-year-old male who is involved in a motorcycle accident as a
pillion rider is brought to the casualty with suspected multiple
injuries. Clinically he has a Glasgow coma scale of 12, a fractured
femur and also has blood at the tip of his penis.
A. Skull x-rays
B. Chest x-rays
C. Cervical spine x-rays
D. Lumbar spine x-rays
E. Pelvic x-rays
95. Pelvic x-rays done show grossly displaced fractures of the pelvis.
You will pass a 24g Foley’s catheter if he goes into acute urinary
obstruction
An intravenous urogram is indicated to make a diagnosis of urethral
rapture
A paralytic ileus is a complication that arises from a retroperitoneal
hematoma
which is best treated by surgical evacuation
A pelvic external fixator when applied helps to stabilize the pelvis and
reduce hemorrhage
The mortality rate from pelvic fractures is about 20%
23
Penicillin should be used as prophylaxis against osteomyetitis
97. The following are complications that can occur following the
treatment of a
Frozen shoulder
Mal-union
98. A 75year old lady presents to the casualty with an intracapsular
fracture of the
24
The risk of recurrent dislocation of the shoulder joint is higher in
patients
below the age of 20yrs
25
CHAPTER 53
INJURIES TO BONE AND JOINTS
ANSWERS
B, E 38. A, B, D, E 75. C
A, C, D 39. B, C, D, E 76. D
A, D 40. B, C, D 77. A, B,
C, D
A, B, C 41. A 78. B, C,
E
A, B, C, E 42. A, C, D, E 79. C, D,
E
A, B, D 43. D 80. B, C
B, C, D 44. B, C 81. A, B,
E
B 45. B, C 82. D
A, B, D 46. B, C, D 83. B, C
D 47. B, D 84. A. B,
26
C
B 48. A, D, E 85.B, D
D 49. B 86. C
B 50. E 87. C
A, B, C, D 51. B, C, E 88. A, B,
C, D, E
A, D 52. A, D 89. A, B,
C, E
B, D 53. C 90. A, C,
D
C 54. A, C 91. C
D 55. A, C, E 92. A, B,
D
D 56. B 93. A, B,
C, D, E
A, B, C, D 57. B, D, E 94. B, C,
E
B, C, D 58. C 95. D, E
A, C, D 59. B 96. C
E 60. C 97. C
C 61. A, B, D 98. A
A, D 62. B, C, D 99. A, C,
E
C 63. B, D 100. C, E
B. D, E 64. A, B, C, D
B 65. C, E
C 66. B
C 67. A, B, C
A, B 68. E
A, B, C 69. B, C, D
A, B, C 70. B
C, D 71. E
C 72. A, C, D
E 73. C
A, B, E 74. C
27
CHAPTER 54
ORTHOPAEDIC SURGERY
1
Absorption from the intestine is stimulated by calcitonin
6. Synovial joints include:
Syndesmosis
Ellipsoid joint
Pivot joint
Gomphosis
Amphiarthrosis
7. Concerning joints:
The co-efficient of friction is very low and equals that of ice
The articular cartilage is avascular and depends on synovia and sub-
chondral
osseous blood supply for nutrition
A detached articular cartilage does not grow
Synovia makes the articular cartilage the slipperiest surface known
Joint space seen on x-ray is the space between the articular cartilages
8. Which of the following is/are transmitted by dominant genes:
Sickle cell disease
Achondroplasia
Haemophilia
Congenital dislocation of the hip
Talipes equino-varus
9. In the grading of muscle power according to the Medical Research
Council
classification grade:
2
pubis and the medial malleolus with the pelvis level
If apparent shortening is equal to true shortening then there is no
abduction deformity
Flexion deformity is measured as the angle at the beginning of
movement
It is always essential to measure Bryant’s triangle to estimate a raised
greater trochanter
11. In the examination of the hip and lower limb:
A positive Trendelenburg’s test indicates a stable hip
A raised greater trochanter is seen in a dislocated hip
Nelaton’s line is undisturbed in coxa vara
Abduction to 90o is possible in a normal adult hip
The level of the pelvis is not of any significance
3
13. The most likely clinical diagnosis is:
Fracture of the upper end of the tibia
Cellulitis
Septic arthritis of the knee
Osteomyelitis of the upper end of the tibia
Haematoma
14. The diagnosis can be confirmed by:
X-ray of the lower leg and knee
Haemoblobin, white blood cell and differential
Erythrocyte sedimentation rate (ESR)
Repeated blood cultures
Aspiration
15. An x-ray of the leg and knee will show:
New bone formation and elevated periosteum
Loss of joint space
Osteolysis
Fracture
No bony abnormality
16. Treatment will include:
Full leg plaster of Paris and analgesics
Bed rest, splintage of the leg in a Thomas’ splint and analgesics
Cloxacillin and ampicillin intravenously for 5 days followed by oral
administration for up to 6 weeks
Aspiration of the knee
Intravenous fluids and/or blood transfusion
4
Osteosarcoma
Brain abscess
Pathological fracture
Bone deformity
Ankylosis of the adjoining joint
19. Acute septic arthritis:
May be caused by N. gonorrhea
Gives rise to joint swelling, restricted active movement but presence of
passive movement
Is best diagnosed by aspiration of the joint
Maybe associated with hyperuricaemia
On x-ray shows Osteolysis of the bones in the joint
A 16-year old boy complains of intermittent pain at the medial lower
end of the
right lower leg for about 2 months. The affected area is slightly warm
and tender.
X-ray shows a cystic area surrounded by sclerotic bone at the lower
end of the tibia.
5
Is caused by E. coli
Presents with recurrent sinuses preceded by painful tender swelling
On x-ray characteristically shows periosteal new bone formation
May lead to squamous cell carcinoma
Is treated by laying the sinus open
23. Tuberculosis of bones and joints:
Is most common in the hip
Is most commonly caused by the bovine type of M. tuberculosis
Is blood-borne usually from the intestinal tract.
Starts in a focus at the metaphysis
May cause meningitis or military tuberculosis
24. Clinical features of tuberculous arthritis include:
Pain in the joint which improves at night when the muscles are relaxed
Limping and restriction of active but not passive movements
Swelling of the joint due to synovial effusion and degeneration
Tenderness of the joint
Pyrexia at night
25. In the investigation of suspected tuberculous arthritis in a 16-year
old boy,
the following MUST be done:
IVP
Culture of early morning gastric washout
Biopsy (needle or open) of synovial membrane
Lumbar puncture
Cystoscopy
26. The general principles in the treatment of joint tuberculosis include:
Immobilization of the joint in the position of function until the symptoms
subside and ESR is normal
Administration of streptomycin, PAS and INAH for at least 18months
Provision of protein-rich diet and vitamin D
Arthrodesis of the affected joint when the disease becomes quiescent
Examination of all contacts
27. In tuberculosis of the spine:
The commonest sites are the lower cervical, upper thoracic and lower
lumbar vertebrae
An abscess from the lumbar spine may present in the iliac fossa, groin,
triangle of Petit or gluteal region
The first radiological sign is destruction of the body of the vertebra
There may be concomitant lung involvement in about 50% of patients
The Mantoux and Heaf’s tests are weakly positive in most patients
6
28. Tuberculous (Pott’s) paraplegia:
Is not likely to arise during treatment of tuberculosis of the spine
Is always spastic in type
May spare the sphincters and sensation
Requires operation only if bed rest and chemotherapy do not produce
some recovery within 3 months
Has a poor prognosis; only about 40% of patients are able to walk
A woman of 25 complains of a painless swelling on the flexor aspect
of the wrist
of 2 months duration. The swelling is found on examination to
extend into the
hand and to be soft, non-tender and with a crepitus on pressure. The
fingers are
held in flexion.
7
Is caused by Staph. aureus
Is treated with tetracyclines or penicillin for 3-4 weeks
If unresponsive to conservative treatment will require the removal of
the nail
May cause osteomyelitis of the phalanx
8
Enchondromata
Limb shortening
Malignant degeneration
Sexual precocity
37. Diaphyseal aclasis:
Is familial with a male preponderance
Affects the growing ends of long and short bones
Results from defective moulding of the metaphysis leaving islands of
bone on the diaphysis
Continues to grow even after cessation of growth of the skeleton
May rarely become malignant
9
If a congenital amputation, then development of the limb stops at any
level
from the elbow to the wrist
If the short bones are absent then it is phocomelia
Is radio-ulnar synostosis if the radius and ulna are joined distally by a
bridge
of bone which prevents pronation and supination
41. Congenital dislocation of the hip:
10
Causes rotation of the face to the affected side
Is managed in the early cases by division of the sterno-mastoid muscle
45. In peripheral nerve lesion:
Axonotmesis is anatomical division of a nerve
Neurotmesis is a lesion in which the Schwann sheath is intact but the
medulla is damaged and undergoes Wallerian degeneration.
Neuropraxia is a lesion in which there is cessation of transmission of
nerve
impulses but no detectable anatomical damage
The rate of nerve growth in neurotmesis is 1mm a day
Recovery is possible in Axonotmesis only if there is surgical
approximation
of the divided ends
46. In peripheral nerve injuries:
Extended elbow with pronated forearm and hand is suggestive of injury
of
the lower trunk of the brachial plexus
Clawing of all fingers of the hand is suggestive of median nerve injury
Foot drop is suggestive of medial popliteal nerve injury
Loss of sensation of the sole of the foot is suggestive of posterior tibial
nerve injury
Analgesia of the dorsum of the thumb, index and middle fingers just
beyond
the distal interphalangeal joint is suggestive of median nerve injury
47. Erb’s palsy:
Results most commonly from difficult breech delivery
Affects the biceps and brachialis
Causes supination of the forearm and extension of the elbow
Untreated, results in a stiff internally rotated shoulder
Has a poor prognosis
11
Causes paralysis only of the hand
Recovers rapidly
Is treated by passive movements
49. Anterior poliomyelitis:
Is an acute inflammation of the cells of the anterior, posterior and
lateral
horns of the spinal cord and motor cells of the brain stem
Is caused by an entero-virus of which there are anti-genetically four
Is endemic with occasional epidemics
Is now rare
Affects mostly people over 5 years
50. In anterior poliomyelitis:
The virus enters the oro-pharynx only by inhalation of droplets
Paralytic poliomyelitis probably accounts for about 20% of cases in
an epidemic
Paralysis is related to injury or vigorous activity during the incubation
period but not to recovery from a debilitating illness
Males are more commonly affected
The incubation is usually 1-2 weeks but may last 5 weeks
51. Symptoms of anterior poliomyelitis include:
Diarrhoea
Photophobia and stiffness of the neck
Paraesthesia, sore throat and headache
Muscle pain and tenderness
Fever, cough and dyspnoea
52. Paralysis in anterior poliomyelitis
Comes on gradually
Reaches a peak in 2-3 weeks and most recovery is within 6 months
of attack
Is flaccid in type
Involves in order of increasing intensity, the lower limbs, trunk and
upper limb
Causes incontinence
12
53. Measures adopted in the treatment of residual paralysis in anterior
poliomyelitis include:
No treatment
Tenotomy
Tendon transplantation
Arthrodesis
Osteotomy
54. In anterior poliomyelitis:
The mortality is about 10%
About 50% have residual paralysis
Elimination from a community can be achieved by the immunization of
most
of the infants
The Salk vaccine is more effective than the Sabin vaccine in prevention
The Sabin vaccine is given orally
55. Cerebral palsy may be caused by:
Rhesus incompatibility
Sickle cell disease
Antepartum haemorrhage
Asphyxia neonatorum
Encephalitis.
56. In spastic paralysis or paresis:
The lesion is in the basal ganglia
The infant has no difficulty in sucking but may have difficulty in holding
up the head later
The hands go involuntarily into flexion at the wrist with adduction of the
thumb
There is ataxia of gait
There may be choreiform movements and hyperkinesia
57. Osteochondritis juvenilis:
Is associated with disturbance of the vascular supply to a segment of
bone and its adjoining cartilage
Affects the metaphysis primarily
Is caused by hormonal imbalance
Is best treated by repeated injection of hydrocortisone with xylocaine
into
the affected joint
Usually takes 12-18 months to settle
13
58. Examples of traction epiphyseal or apophyseal type of
Osteochondritis
juvenilis include:
Synovitis
Tuberculous arthritis of the hip
Septic arthritis of the hip
Osteochondritis of the femoral capital epiphysis
Irritable hip
60. In Perthes’ disease:
The male/female ratio is ¼
Late cases have limitation of abduction and internal rotation
X-ray may show a small or fragmented opaque capital epiphysis
Most patients under 6 years do well with or without treatment
Treatment averts deformity in most patients over 9 years
61. Blount’s disease (osteochondrosis deformans tibiae)
Is seen all over the world
Results from disturbance of growth at the lateral aspect of the upper
tibial metaphysis
Results in genu valgum
If bilateral, the child may be so deformed as to walk with the pelvis a
few
inches from the ground
Is treated by tibial osteotomy
62. Idiopathic slipped upper femoral epiphysis:
14
Is a gradual downward and anterior displacement of the femoral capital
epiphysis in adolescents.
Causes limitation of external rotation and adduction
May be associated with hypogonadism
Is bilateral in about 40% of patients
Is best treated by reduction
63. Osteoarthritis:
Is an atrophic degenerative joint disease
Causes limitation of external rotation and adduction
Maybe be associated with hypogonadism
Is bilateral in about 40% of patients
Is best treated by reduction
64. Osteoarthritis may be caused by:
Genu valgum
Septic arthritis
Intra-articular cortisone therapy
Delayed union of a fracture
AS disease
65. In osteoarthritis:
There is fragmentation of the articular cartilage
The synovial membrane is thin
Young blood vessels invade the peripheral articular cartilage
There is friction on the subchondral bone
The adjoining bone undergoes osteolysis
66. The characteristic clinical symptoms of osteoarthritis is/are:
Increasing stiffness
Pain
Crepitus
Deformity
Swelling
67. The pain in osteoarthritis:
15
Is initially intermittent and later becomes constant
Occurs on movement
Is not relieved by rest
Arises from spasm of local muscle and not from the joint
Is not referred to another joint
68. In osteoarthritis of the hip, the joint is:
Abducted
Internally rotated
Flexed
Ankylosed
Externally rotated
16
Is produced by the basophil cells of the anterior pituitary
Stimulates protein synthesis and growth
Enhances glucose uptake by the cells
If produced excessively before epiphyseal fusion leads to acromegaly
If deficient in childhood leads to a dwarf with small trunk, small limbs,
big
head and normal intelligence
73. Features of acromegaly include:
Increased height
Prominent mandible
Thickening of face
Prominent supra-orbital ridge
Long limbs
74. Bone is affected by:
Thyroxine
Testosterone
Oestrogen
Cortisol
Glucagon
75. In osteoporosis:
There is a reduction in bone mass per unit volume
Osteoid formation is normal
Calcification of osteoid is deficient
Post-menopausal women are more commonly affected
The long bones are more affected than the vertebrae and pelvis
76. Aetiological factors in osteoporosis probably include:
Increased muscular activity
Thyrotoxicosis
Diminished ACTH production
Inadequate intake of protein and Vit. C
Diminished progesterone output
77. In osteoporosis:
17
Most patients have severe bone pain
The patient may present with fracture of the spine, neck of femur,
neck of humerus or lower end of the radius
There is progressive loss of height
The serum alkaline phosphatase is elevated
The serum calcium is depressed
78. SPECIFIC treatment for osteoporosis includes:
Calcium 3g/day
Large doses of Vit. C
Thyroxine
Bisphosphonates
Oestrogens
79. Paget’s disease (osteitis deformans):
Is generalized affection of the skeleton in middle aged and elderly men
but not women
Is characterized by hardening of the bones
Is caused by deficiency of testosterone
May cause pathological fractures
Becomes sarcomatous in about 25% of patients
80. Paget’s disease:
Is asymptomatic in most patients
Leads to kyphosis and stooping
Leads to genu valgum
May result in cardiac failure because of frequently associated
valvular affections
May shorten the height
18
Subperiosteal haematoma
Fever
Bleeding gums
Sabre tibia
Separation of the epiphyses
83. Rickets:
Is seen in children and adolescents
Is in all patients caused by inadequate Vit. D intake
Results in failure of calcification of osteoid to osseous bone
Pathologically gives rise to a wide, thick cartilage zone of the
epiphyseal growth plate
Is now rare in the world because of routine administration of Vit. D to
children
84. Clinical features in rickets include:
Diarrhoea and vomiting
Tetany
Knock knees but not bow legs
Thickening and widening of the wrists
Bossing of the frontal, parietal, costal and phalangeal bones
85. In rickets:
The serum alkaline phosphatase is normal
The serum phosphorous is usually low
The blood urea may be elevated
The urine phosphate may be elevated
The faecal fat may be more than 6g daily
86. In the treatment of rickets:
Vit.D 1,000 i.u. given daily gives dramatic results
The serum calcium, phosphate and alkaline phosphatase are
checked monthly
Hypocalcaemia or hypercalcaemia may occur
Oral calcium 1g should be given daily
Bony deformities may recover spontaneously
87. Osteomalacia:
Is uncommon and is generally seen in elderly women and rarely in
pregnant or lactating women
19
May deform the pelvis
May complicate Billroth I partial gastrectomy
Is confirmed by biopsy of the iliac crest
Is treated with Vit. D 2,000 i.u. and calcium 1g daily
A 1-year old male child has swollen limbs, which he cannot move. He
is restless.
The gums bleed easily.
20
93. Osteomyelitis in sickle cell disease is characterized by:
Asymmetrical involvement of the bones
Diaphyseal involvement
Refraction to medical treatment in the early stages
Multifocal distribution
Severe septicaemia
94. In prolapse of lumbar intervertebral disc:
The annulus fibrosus is degenerated
The anterior longitudinal ligament is frayed
The nucleus pulposus herniates into the neural canal following an
extension injury
Sneezing may be a precipitation trauma
The commonest site is L3-4
A 40-year old man is suspected of having a prolapsed lumbar
intervertebral disc
has pain in the right lumbar area which radiates over the right
buttock behind the
thigh and calf into the foot.
21
There is degeneration of the cartilaginous plates over the vertebral
bodies
The annulus fibrosis remains intact
Pain is centered in the spine and associated with stiffness and
limitation
of spinal movements
X-ray shows narrowing of the intervertebral joints and new bone
formation
at the periphery
22
ESR
Serum alkaline phosphatase
101. Measures taken in the management of muscular or ligamentous
strain of
the spine include:
A. Rest in bed
Short wave diathermy and massage
Wearing of surgical corset
Operative exploration
Muscle strengthening exercises
102. Cancellous osteoma:
A. Is a true tumour
Is found commonly at the end of long bones
Continues to grow throughout life
May undergo malignant change
Is usually symptomless
23
Arises at the junction of the epiphysis and the metaphysis and
spreads
to the epiphysis
Normally penetrates into the joint
Is a spindle-cell tumour with giant cells formed by coalescence of
some of
the spindle cells
Is benign in 50% and frankly malignant in 15% of cases, and the rest
though
benign recur after removal
Affects the 10-20 age group
106. The common sites of osteoclastoma include the:
A. Scapula
Lower end of the femur
Lower end of the tibia
Pelvis
Lower end of the radius
107. Treatment of osteoclastoma may be by:
A. Amputation
Excision
Curettage and bone graft
Radiotherapy
Cytotoxic therapy
108. Enchondroma:
Is a true tumour arising usually in the metaphysis or shaft of the short
long
bones of the hand or feet
Is usually seen in children
May produce a pathological fracture
Shows on x-ray as a sclerotic zone within the bone with cortical
24
ballooning
Is treated by excision
109. Benign chondroblastoma:
A. Is seen in adolescents under 20yrs
Is more common in females
Histologically consists of young cartilage cells with areas of giant cell
transformation, myxoid and collagenous cells
Starts in the epiphysis
May rarely recur after excision or curettage and show malignant
characteristics
110. Bone ‘swellings’ originating from osteoblast include:
A. Fibrous osteoma
Ossifying fibroma
Osteochondroma
Aneurysmal bone cyst
Osteoclastoma
111. A simple bone cyst:
A. Is common in children but rare in adults
B. May involve any bone
Arises in the epiphysis
Is usually symptomless
Is treated by excision
112. A solitary radiolucent lesion in the metaphysis of the femur in a boy
15
may be:
A. Non-ossifying fibroma
Chondroma
Osteoclastoma
Solitary bone cyst
Benign chondroblastoma
113. Osteosarcoma:
A. Is the commonest bone tumour
Is usually metaphyseal in origin
Contains elements of bone and cartilage but not of fibrous tissue
Arises from primitive spindle cells
Does not arise from extra-osseous tissue
25
114. Osteosarcoma may arise from:
A. Cancellous osteoma
Enchondroma
Osteochondroma
Osteitis deformans
Ossifying fibroma
115. Osteosarcoma spreads mainly to the:
A. Lymph nodes
Liver
Lungs
Brain
Other bones
116. Osteosarcoma:
A. Has a peak incidence in the first decade
Occurs around the knee in 50% of patients
Has a male/female ratio of 1.5/1
Does not present with pathological fracture
Presents with a painful, tender, warm swelling
117. Radiological features of osteosarcoma include:
A. Diaphyseal bone destruction
Soft tissue mass or bone formation
Radiate bone spicules of the cortex in the affected area
Dense sclerosis of the rest of the bone
Triangular condensation of bone at the site of periosteal elevation
118. The most essential investigation after establishing a diagnosis of
osteosarcoma is:
A. Skeletal survey
X-ray of the lungs
Blood profile
E.S.R
Serum alkaline phosphate
119. The present acceptable forms of treatment of osteosarcoma
include:
A. Amputation followed by cyclical combination cytotoxic therapy
Radiotherapy followed by amputation
Cytotoxic therapy followed by local resection
Amputation
Cyclical combination cytotoxic chemotherapy
26
120. Cytotoxic drugs currently used in the treatment of osteosarcoma
include:
A. Methrotrexate
Actinomycin D
Vincristine
Cyclophosphamide
Doxorubicin
121. An x-ray shows a disappearing bone. The conditions to consider
include:
A. Osteoclastoma
Aneurysmal bone cyst
Angiosarcoma
Neurofibromatosis
Histoplasmosis duboisii
A 50-year old man complains of recurrent pain in the ribs. X-rays of
the ribs, skull
and pelvis shows numerous areas of punched out rarefactions
without expansion
of the cortex. The lungs are clear.
27
“onion peel”
appearance is indicative of:
A. Multiple myeloma
Osteoclastoma
Fibrosarcoma
Syphilitic periostitis
Ewing’s tumour
28
128. The treatment of choice is:
A. Radiotherapy
Curettage and bone grafting
Above-knee amputation
Excision of the upper end of the fibula
Leave alone
129. In DeQuervain’s disease the following is/are involved:
A. Abductor pollicis brevis
Extensor pollicis brevis
Radial tubercle
Flexor carpi radialis
Abductor pollicis longus
29
sewing
or writing
The cause is compression of the ulnar nerve beneath the flexor
retinaculum
The thenar muscles may be wasted
Injection of hydrocortisone in xylocaine into the space has not been
found beneficial
133. Mallet finger:
A. Is partial flexion deformity of the distal interphalangeal joint
Is caused by rupture of the middle slip of the extensor tendon
expansion
of the finger
Is painful
If seen within a week should be treated by immobilization of the
finger with
the tendon relaxed
If old should be ignored
30
Fracture of the greater tuberosity of the humerus
135. Acute tendinitis of the shoulder:
A. Occurs at all ages
B. Is associated with a calcareous deposit above the greater tuberosity
of the humerus
Causes sudden intense pain in the shoulder
May be associated with fever
Is treated by local injection of hydrocortisone in xylocaine or oral
phenylbutazone and a course of antibiotics
136. Pericapsulitis or frozen shoulder syndrome:
139. Ainhum:
31
A. Occurs in all races
Is a progressive deepening constricting groove which encircles the
base of a toe
Affects the second toe most commonly
Is caused by infection
May result in auto-amputation
A 50yr old woman presents to the orthopedic clinic with increasing
pain in the
right thigh of 3 months duration. The pain does not respond to
Paracetamol and
anti-inflammatory drugs. She had had a mastectomy 4 years earlier
for breast
cancer. Preliminary x-rays show an osteolytic lesion in the proximal
third of the
femur.
32
C. Sickle cell bone pain crises
D. Non accidental fracture of the proximal humerus
E. Malaria
33
Myositis ossificans of the shoulder
146. A 12yr old boy presents with rapidly growing painful lump in the
proximal tibia
of three months duration. X-rays suggest an osteosarcoma of the
tibia. Your management will include:
148. Rickets:
A. It’s a defect in the mineralization of physis
Low calcium is a characteristic feature
Vitamin-D resistant rickets is X-linked dominant
Physeal cupping is characteristic in x-rays
Vit-D treatment resolves most deformities
149. Club foot deformities have the following components:
A. Forefoot pronation
Forefoot supination
Ankle equinus
Hind-foot varus
Mid-foot recurvatum
150. Hallux valgus:
A. Is common amongst elderly men
Has a genetic predisposition
Can occur in adolescent girls
Is bilateral in 50% of cases
Is always treated by surgery
34
CHAPTER 54
ORTHOPAEDIC SURGERY
ANSWERS
A, D 42. A, B, C 83. C. D
124. E
B, E 43. B, D 84. B, D
125. A, C
B, E 44. B, C 85. B, C, D, E
126. B, C
B 45. C 86. E
127. E
A 46. D, E 87. A, B, D
128. D
B, C 47. B, D, E 88. C
129. B, E
B, D 48. A, B 89. B, D
130. B, E
35
B 49. C 90. B, C
131. B, D
C, E 50. E 91. A, B
132. A
A, D 51. A, B, D 92. B, C, E
133. A
B 52. C 93. B
134. C
A, B, D, E 53. A, B, C, D, E 94. A, D
135. B, C
D 54. A, E 95. E
136. A, B, E
D 55. A, C, D, E 96. A
137. C, D, E
E 56. C 97. A, B, D, E
138. A. D
B, C, E 57. A, E 98. B, D
139. B, E
A, D 58. C 99. C, D, E
140. A, C, D
B, C, D 59. D 100. A, D, E
141. B, C, D
A, C 60. B, C, D 101. B, C, E
142. A, B, D
D 61. D, E 102. B, E
143. B, D
C 62. C 103. B, E
144. B
B, D 63. E 104. A, B, C
145. A, C, D
E 64. A, B, C 105. A, C, D
146. A, B, D, E
C, D, E 65. A, C, D 106. B
147. A, B, C, E
C 66. A, B, C, D, E 107. A, B, C, D
148. A, C, D, E
A, C, E 67. A, B 108. C
149. B, C, D
B, D 68. C 109. A, C, D, E
150. B, C, D
C 69. C, D 110. A, C, E
C 70. A, C, D 111. A, B, D
D 71. B, D, E 112. A, B, D, E
D, E 72. B 113. B, D
A, D 73. B, C, D 114. C, D
C 74. A, B, C, D 115. C
36
B, C 75. A, D 116. C, E
D, E 76. B, D 117. B, C, E
B, C 77. B, C 118. B
A, C, E 78. D 119. A, C
C 79. D 120. A, C, D, E
A, C 80. A, B, E 121. B, C, D, E
A 81. A, C, E 122. B, C
C, D 82. A, C 123. A, B, D
37
CHAPTER 52
NEUROSURGERY
1. Congenital abnormalities of the C.N.S.:
1
Irritability and somnolence
Poor suckling
Frequent epileptic fits
Reduced vision or blindness
Absent tendon jerks
2
CT scan
9. The Spitz-Holter or Pudenz valve is used for:
A. Ventricular tap
B. Ventricular-peritoneal shunt
C. Ventriculo-atrial shunt
D. Ventriculo-umbilical shunt
E. Ventricula-peritoneal shunt
10. Craniosynostosis:
A. Is closure of one or more cranial sutures
B. Affects most commonly the sagittal suture
C. May lead to blindness
D. Does not cause mental retardation
E. Should be corrected before the baby is 4 months and preferably in
the
neonatal period
11. Spina bifida:
A. Is a congenital deformity of the spine characterized by incomplete
closure of the vertebral canal
B. Is a midline fusional defect which occurs in the first 4 months of
embryonal
life
C. Occurs most frequently in the thoracolumbar junction
D. Has an incidence of 10 per 1,000 births
E. May be associated with a similar deformity of the spinal cord
12. Associated factors in spina bifida include:
A. Heredity
B. Drugs
C. Conception before 17 or over 30 years
D. Geographical location – England, Nigeria, U.S.A
E. Hydramnios
3
13. In spina bifida occulta:
A. The spinal defect is not obvious
B. There are hair patches and portwine staining at the site
C. There may be limping when the child begins to walk and the tendon
jerks
are brisk
D. Nocturnal enuresis and delay in bladder control may occur
E. Hemivertebrae or fusion of 2 or more vertebrae may be present
4
D. Should be excised and the dura repaired
E. Has an excellent prognosis
17. Myelomeningocele:
A. Is an uncommon variety of spinal bifida
B. Is usually in the thoracic or cervical region
C. Is sessile and covered by atrophic skin
D. Is always associated with hydrocephalus
E. Should always be treated
5
bone.
You will advise:
A. Deferred treatment for a few months
B. Excision of the swelling
C. No treatment at all
D. Aspiration
21. Intracerebral abscess:
A. Is generally solitary and unilocular but may be multiple or multilocular
B. Is usually primary but may be secondary to an adjacent or distant
primary
source
C. Is most commonly caused by pneumococcus or streptococcus
D. Is formed in the grey matter
E. Occurs most frequently in the occipital and parietal lobes
6
Africa
now is:
A. Plain skull x-rays
B. E.E.G.
C. Angiography
D. Ultrasonography
E. CT scan
25. Complication(s) of intracerebral abscess include:
A. Dementia
B. Epilepsy
C. Neurological deficits
D. Recurrent headaches
E. Meningitis
7
C. Chlorpromazine
D. Phenytoin sodjum
E. Mephenesin carbamate
28. Methods used in the management of idiopathic trigeminal neuralgia
include:
A. Xylocaine block
B. Alcohol block
C. Radio-frequency coagulation
D. Infra-orbital nerve avulsion
E. Section of the trigeminal nerve
29. The commonest intracranial tumour is:
A. Meningioma
B. Metastases
C. Glioma
D. Neurilemmoma
E. Pituitary adenoma
8
E. Medulloblastoma
32. Astrocytoma:
A. Arises from glial cells
B. Is the commonest C.N.S. primary tumour
C. In adults is not as frequent in the cerebral hemispheres as other
tumours
D. Of the cerebellum occurs more commonly in children
E. Of the cerebellum is usually of grade 3 or 4
33. Medulloblastoma:
A. Is more prevalent in the elderly
B. Usually involves the vermis of the cerebellum
C. Is slow-growing
D. May spread through the subarachnoid space
E. Is highly cellular with small cells forming incomplete or pseudo-
rosettes
34. Meningioma:
A. Arises from the endothelial cells of the arachnoid villi
B. Is always solitary
C. Is not well-encapsultated
D. May develop as a carpet-like tumour over the inner surface of the
dura
E. Can invade the brain, destroy the bone, and metastasize to distant
organs
9
36. Basophilic adenoma:
A. Nearly always secretes ACTH to cause Cushing’s syndrome
B. Is more common in females
C. Is more common in young adults
D. Enlarges the sella turcica
E. Affects the optic chiasma
37. Tumours of development origin include:
A. Glomus jugulare
B. Craniopharyngioma
C. Chordoma
D. Chromophobe adenoma
E. Paraphyseal cyst
38. Intracranial dermoid cyst:
A. Is usually found in the anterior cranial fossa
B. Is spherical and well-encapsulated
C. Contains sebaceous material and hair
D. May communicate with a dermal sinus
E. May be the cause of granulomatous meningitis
10
E. Is probably due to displacement of the cranial nerves and meninges
40. In intracranial tumours:
A. There may be vomiting which is worse in the evening
B. Vomiting is usually associated with abdominal discomfort
C. Vomiting is more common in posterior fossa neoplasms
D. A seizure may be the initial symptoms
E. Insomnia may be an early symptom
41. Clinical features of intracranial tumours include:
A. Impairment of judgement, lack of insight
B. Enlarging head in children under 5 years
C. Papilloedema
D. Tachycardia and elevation of the blood pressure
E Alertness
42. Localizing signs in frontal lobe tumours include:
A. Progressive intellectual impairment accompanied by loss of critical
judgement and memory
B. Loss of two point discrimination
C. Urgency of micturition followed by incontinence
D. Contralateral homonymous hemianopia
E. Bilateral spastic paraparesis
11
C. Acalculia (inability to do simple arithmetic)
D. Progressive deafness and tinnitus
E. Inability to find one’s way in familiar surroundings
44. Clinical features of occipital lobe tumours include:
A. Inability to recognize colours
B. Ipsilateral homonymous hemianopia
C. Inability to recall the appearance of familiar objects
D. Dysphasia
E. Auditory hallucinations
45. Clinical features of temporal lobe tumours include:
A. Contralateral homonymous hemianopia
B. Dysphasia
C. Hemiparesis
D. Hallucination of unpleasant taste or smell followed by cloudiness
of consciousness
E. Narcolepsy
46. A 9-years old boy has been having paroxysmal headache and
intermittent
“swelling” of his head. He also has polyuria without glycosuria
and
narcolepsy. He has noticed enlargement of his penis, hair over the
12
chest,
pubis and face.
13
movements and past pointing on reaching an intended target for
two months
suggest a tumor of the:
A. Cerebellar hemisphere
B. Occipital lobe
C. Parietal lobe
D. Temporal lobe
E. The medulla
50. Clinical features of chromophobe adenoma of the pituitary include:
A. Loss of libido
B. Visual loss
C. Optic atrophy
D. Parkinsonism
E. Loss of 2-point discrimination
51. Acromegaly is caused by:
A. Craniopharyngioma
B. Chromophobe adenoma of the pituitary
C. Basophilic adenoma of the pituitary
D. Temporal lobe tumour
E. Acidophilic adenoma of the pituitary
52. Headache, loss of upward gaze, ptosis, and dilatation of the pupils
14
suggest a tumour of the:
A. Mid-brain
B. Pineal gland
C. Pons
D. Fourth ventricle
E. Cerebellar hemisphere
53. New bone formation (hyperostosis) in a plain X-ray of the skull is
suggestive of:
Oligo-dendroglioma
B. Astrocytoma
C. Meningioma
D. Craniopharyngioma
E. Metastases from carcinoma of the breast
54. A plain X-ray of the skull in raised intracranial pressure may show:
A. Enlargement and ballooning of the sella
B. Sclerosis of the anterior and posterior clinoid processes
C. Splaying of sutures
D. Diminished vascular markings
E. Osteolysis of the inner table
55. Features suggestive of an intracranial tumour in a plain X-ray of
the
skull include:
Abnormal intracranial calcification
Abnormal vascular markings
Displacement of the pineal gland of more than 3mm
Narrowing of exit foramina of cranial nerves and vessels
New bone formation
15
56. Very useful investigations in suspected intracranial tumours
include:
A. E.E.G
B. Angiography
C. Cat-scan
D. Ventriculography
E. Plain X-ray of the chest
57. The following may have clinical features like those of an intracranial
tumour:
A. Cerebrovascular accident
B. Chronic subdural haematoma
C. Chronic intracerebral abscess
D. Uraemia
E. Dementia
58. Radiotherapy only is used in the treatment of:
A. Astrocytoma
B. Meningioma
C. Oligodendroglioma
D. Medulloblastoma
E. Ependymoma
59. Radiotherapy is given after surgical extirpation of:
A. Craniopharyngioma
B. Pituitary adenoma
C. Choroid plexus papilloma
D. Pinealoma
E. Neurilemmoma
16
60. Gliomas respond to:
A. CCNU
B. Vincristine
C. BCNU
D. Mithramycin
E. Procarbazine
61. The commonest benign tumour of the skull is:
A. Chondroma
B. Fibroma
C. Osteoma
D. Osteoclastoma
E. Haemangioma
62. A one-year old baby has a spherical swelling over the anterior
fontanelle.
It is soft, fluctuant, non-tender, and does not enlarge when the
baby cries.
It appears to be loosely attached to the overlying aponeurosis and
underlying
pericranium.
17
63. In arterio-venous malformations of the scalp:
A. The arteries and veins are abnormal in caliber, length and number
B. Intervening capillaries are dilated and tortuous
C. The outer table of the skull is always indented
D. There may be an intracranial communication
E. There is no increase in size with time
64. Subgaleal haematoma:
A. Occurs only in the newborn
B. May be caused by vacuum extraction or accident
C. Lies between the pericranium and aponeurosis and causes pain,
tenderness, fever and toxicity
D. Spreads diffusely in the scalp and is not localized
E. Is treated by incision and drainage
65. A vascular, protuberant, non-tender, firm, swelling about 5 cm
wide with
indefinite edge in the occipital region of the scalp in a 45 year old
woman
may be:
A. Turban tumour
B. Malignant angioendothelioma
C. Haemangiopericytoma
D. Epithelioma
E. Fibrosarcoma
18
66. A 55-year old man complains of right sciatic pain of 2 months
duration. The
hamstrings and calf muscles of both sides are wasted and the
knee jerks are increased but the ankle jerks are absent. There is
no fever or any other abnormality.
19
B. Kidney
C. Lung
D. Liver
E. Thyroid
20
C. Subarachnoid haemorrhage
D. Ophthalmoplegia
E. Extradural haemorrage
21
C. MRI is the investigation of choice
D. Chemotherapy is never indicated
E. High dose corticosteroids are useful
22
A. A neuropraxia refers to “concussion” of the nerve i.e. transient event
B. Neurotmesis refers to transaction of the nerve
C. Neuropraxia usually presents with muscle atrophy
D. In axonometsis both the myelin and axon are lost
E. Recovery is possible in neurotmesis
23
hippocampus is important in the pathogenesis
E. CT scan is the study of choice
CHAPTER 52
NEUROSURGERY
ANSWERS
1. C 38. B, C, D, E 75. B
2. A, B, D 39. A, D 76. B, C, E
3. C, D, E 40. C, D 77. A, B, C, E
4. A, B, D 41. A, B, C 78. A, B, D, E
5. B, D, E 42. A, C 79. A, B, E
6. A, C, E 43. B, C, E 80. A, B, E
7. B, D, E 44. A, C 81. A, B
8. E 45. A, B, C, D 82. A, B, C
9. B, C, D, E 46. D 83. A, B
12. A, E 49. A
13. A, B, D, E 50. A, B, C
14. A, D, E 51. E
15. A, D 52. A, B
16. C, D, E 53. C
17. C 54. A, C
18. A, B, C, D 55. A, B, C, E
19. C 56. A, B, C, D, E
24
20. C 57. B, C
21. A 58. D
22. A, B, C, D, E 59. A, B, D
23. A, B, D 60. A, B, C, D, E
24. E 61. C
25. B, C, E 62. D
26. A, C 63. A, D
27. B, D, E 64. B, D
28. B, C, D 65. D, E
29. C 66. C, D
30. A, C, E 67. E
31. A, B, E 68. C, E
32. B, D 69. B, C, E
33. B, D, E 70. E
34. A, D 71. A, C, D, E
35. A, C 72. B, E
36. B 73. A, C, D
37. B, C, E 74. C
25