Palmer Ultrasound Imaging

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Manual of
diagnostic ultrasound
Edited by
P. E. S. Palmer
University of California
Davis, California, USA
World Health Organization
Geneva
1995
Reprinted 1999, 2000, 2002
WHO Library Cataloguing in Publication Data
Manual of diagnostic ultrasound / edited by P. E. S. Palmer.
l.Diagnostic imaging 2.Ultrasonography I.Palmer, P. E. S.
ISBN 92 4 1544619 (NLM Classification: WB 289)
The World Health Organization welcomes requests for permission to reproduce
or translate its publications, in part or in full. Applications and enquiries should
be addressed to the Office of Publications, World Health Organization, Geneva,
Switzerland, which will be glad to provide the latest information on any changes
made to the text, plans for new editions, and reprints and translations already
available.
World Health Organization, 1995
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Authors
The World Health Organization is grateful to the authors ofthis manual
who freely contributed their time and expertise in its production:
B. Breyer
University of Zagreb. Zagreb. Croatia
c. A. Bruguera
Diagnostic Imaging Teaching Institute. Buenos Aires. Argentina
H. A. Gharbi
University of Tunis. Tunis. Tunisia
B. B. Goldberg
Thomas Jefferson University. Philadelphia. United States of America
F. E. H. Tan
College of General Practitioners. Kuala Lumpur. Malaysia
M. W. Wachira
University of Nairobi. Nairobi. Kenya
F. S. Weill
University of Besam;on. Besanc,;on. France
v
Contents
Preface
vii
Acknowledgements
ix
Glossary
xi
Chapter 1 Basics of ultrasound
1
Chapter 2 Choosing an ultrasound scanner 17
Chapter 3 Basic rules of scanning 25
Chapter 4 Acoustic coupling agents 43
Chapter 5 Abdomen
47
Chapter 6 Abdominal aorta
53
Chapter 7 Inferior vena cava
65
Chapter 8 Liver
71
Chapter 9 Gallbladder and biliary tract 91
Chapter 10 Pancreas
III
Chapter 11 Spleen
125
Chapter 12 Peritoneal cavity and gastrointestinal tract 137
Chapter 13 Kidneys and ureters 151
Chapter 14 Urinary bladder
175
Chapter 15 Scrotum and testis
187
Chapter 16 Gynaecology (non-pregnant female pelvis) 195
Chapter 17 Obstetrics
223
Chapter 18 Neonates
283
Chapter 19 Neck
297
Chapter 20 Pericardium
309
Chapter 21 Pleura
313
Chapter 22 Ultrasound-guided needle puncture 317
Annex. Specifications for a general purpose ultrasound scanner 321
Index
325
Preface
Diagnostic imaging is recognized as an important adjunct to clinical
examination in the care of patients with many common illnesses. Most
such imaging will be by radiography (X-rays) or ultrasound. In pursuit
of the World Health Organization's goal of health for all, many of the
examinations will be performed at the first referral level, where patients
will be seen, referred from primary care or in need of emergency
treatment. Many countries do not have sufficient radiologists or sonolo-
gists to provide skilled techniques and interpretation, and imaging may
be requested, interpreted and often performed by medical officers with
little or no speCialist training or experience.
This manual is one of several published by the World Health Organization
to provide guidance on the use of diagnostic imaging by non -specialists.
l
The use of ultrasound is increasing rapidly worldwide; it is particularly
important in obstetrics, but also provides useful information about the
abdomen and soft tissues. Because there is no ionizing radiation,
ultrasound should be the preferred method of imaging whenever it can
give useful clinical information.
The manual is a basic reference text to help with technique, recognition
of the normal, and differential diagnosis. It indicates the clinical
situations in which ultrasound scanning is likely to prOvide gUidance for
the care of the patient, and those in which scanning will not be reliable
or helpful. The decision to scan is based on many factors and each
individual patient's needs must be taken into account.
The safety of ultrasound has been a subject of considerable discussion
and study. Mter three decades of use and the examination of thousands,
probably millions, of people, the question of absolute safety is still being
debated. The potential risks, if any, also need to be Wf' 6hed against the
benefits, particularly in obstetrics, where ultraso' .od provides much
information that cannot be obtained in any o t h ~ way.
For a small hospital or clinic, radiography (such as is provided by the
WHO Radiological System) should remain the first choice of imaging
technique, although ultrasound may be tempting because the equipment
is less expensive and apparently less complicated. However, ultrasound
cannot image the lungs, fractures or most skeletal abnormalities: its
limitations must be recognized.
Ultrasound is very operator-dependent. In its report,
2
a WHO Scientific
Group stated ''The difficulties in making an accurate diagnosis from
ultrasound images are such that the purchase of ultrasound equipment
without making prOvision for the training of an operator is contrary to
good health care practice and is unlikely to be cost effective." Proper
training and experience are required, preferably with teachers who are
highly skilled and who have practised ultrasound for many years. The
Group concluded that a physician needs at least one month's full-time
training in a busy ultrasound department to achieve even a minimum
1 Manual oj darkroom technique (1985), Manual oj radiographic interpretationJor general
practitioners (1985). and Manual oJ radiographic technique (1986).
2 Future use oj new imaging technologies in developing countries: report of a WHO Scientific
Group. Geneva. World Health Organization, 1985 (WHO Technical Report Series, No.
723).
vii
viii Preface
level of expertise. This would amount to at least 200 obstetric and
abdominal examinations made under supervision. For a physician to go
on to become a competent sonologist, the Group recommended at least
six months' full-time training in a recognized centre, and even then
further experience would be advisable under supervision. They concluded
that "Wherever possible, ultrasound examinations should be carried
out by trained physicians", and went on to add that if non-physicians
are to perform examinations, they need to have had at least one year's
full-time training in ultrasound and preferably a background in
radiography or nursing; they should always work under the supervision
of an experienced sonologist.
The authors of this manual fully endorse these recommendations and
only agreed to prepare this manual because they recognized that for
many users of ultrasound there will not be experts to whom patients or
scans can be sent when interpretation is difficult. This manual is not
meant to take the place of proper training, nor is it meant to replace the
textbooks already available. On the contrary, it is a supplement to these
to help the less experienced who may not have reached the level of
knowledge and skill so often taken for granted by more comprehensive
texts.
The manual also provides guidance on the standards by which ultrasound
equipment may be judged. There are many varieties of such equipment
and too often there is no independent expert to guide the practitioner in
the purchase of a unit. Particularly, there is not always information
about the shortcomings and inadequacies of what may appear to be a
bargain. The WHO Scientific Group mentioned above provided
specifications for a general purpose ultrasound scanner (GPUS). Updated
speCifications are included in this manual and any product that meets
them will produce quality ultrasound images. The GPUS, as its name
implies, is suitable for all general purpose studies at any level of medical
care and will only be bettered by much more expensive ultrasound units.
It is hoped that the use of this manual will not be limited to general
practitioners, and that it will provide a starting-point for medical
students, midwives and those training to be speCialists in diagnostic
imaging. In many places ultrasound is the only scanning technique
readily available. Unfortunately, in some countries it has already gained
a reputation for unreliability because it has been used by people who,
as a result of insufficient training, have made many errors of diagnosis.
In this way it can be dangerous. It is hoped that this manual will
stimulate the interest and expand the knowledge ofthose who use it, so
that it becomes part oftheir training and leads to much wider and deeper
understanding of this very important imaging technique.
The authors realize that this manual will not meet the needs of everyone.
Comments and suggestions will be welcome and of considerable value
for a revised edition. All correspondence should be addressed to Chief,
Radiation Medicine, World Health Organization, 1211 Geneva 27,
Switzerland.
Acknowledgements
The authors and editor would like to record their appreciation of the
unsparing help provided by Dr V. Volodin. Medical Officer. Radiation
Medicine. WHO. Geneva. We were fortunate to have the thoughtful and
skilled professional guidance of Dr P. A. Butler. Head. Technical
Publications. WHO. Professor Asim KUIjak (Zagreb) was particularly
helpful. and Dr W. E. Brant (Davis) gave much useful advice and
practical help with the illustrations. The World Federation of Ultrasound
in Medicine and Biology (WFUMB) gave welcome information and
support. Appreciation must be also recorded for the support provided by
many colleagues. in particular:
In Sacramento. Dr Gilland Dea;
In Nairobi. the staff of the Nairobi X-ray Centre;
In Philadelphia. Dr L. Needleman and Dr Ji-Bin Liu. with MrT. L. Berry
and Ms R. A. Curry;
In Rijeka. Professor Z. Fuckar;
In Tunis. Dr K. Abdesselem-Ait-Khelifa. Dr 1. Bardi. Dr F. Ben Chehida.
Dr A. Hammou-Jeddi and Dr R. Slim;
In Yonago. Professor K. Maeda;
In Zagreb. Mr V. AndreiC.
Extra scans were provided by Professor B. J. Cremin of Cape Town.
South Mrica. and Dr Sam Mindel of Harare. Zimbabwe.
Without the willing assistance of all these people. it would have been
difficult to produce this manual.
The staff of Illustration Services. University of California. Davis. provided
many innovative ideas for the production of this manual. Particular
appreciation goes to Claudia R. Graham for the illustrations and layout
ofthe pages. and Craig F. Hillis and Rick Hayes for computer and design
assistance. The scans were obtained from many parts of the world and
together with the accompanying low-contrast reference images were
reproduced by Illustration Services. University of California. Davis.
ix
Glossary
Acoustic beam
Acoustic
enhancement
The beam of ultrasound waves (energy)
produced by the transducer (probe). May be
divergent, focused or parallel.
The increased echogenicity (echo brightness)
of tissues that lie behind a structure that
causes little or no attenuation of the ultrasound
waves, such as a fluid-filled cyst. The opposite
to acoustic enhancement is acoustic shadowing
(q.v.).
Acoustic impedance The resistance offered by tissues to the
movement of particles caused by ultrasound
waves. It is equal to the product of the density
of the tissue and the speed of the ultrasound
wave in the tissue. It is because tissues have
different impedances that ultrasound can
provide images of the part of the body being
scanned.
Acoustic shadowing The decreased echogenicity of tissues that lie
behind a structure that causes marked
attenuation of the ultrasound waves. The
opposite to acoustic shadowing is acoustic
enhancement (q.v.).
Acoustic window
Anechogenic
(anechoic)
Artefact
Attenuation
A tissue or structure that offers little obstruction
to the ultrasound waves, and can therefore be
used as a route to obtain images of a deeper
structure. For example. when the bladder is
full of urine it forms an excellent acoustic
window through which the pelvic structures
may be imaged. Similarly, it is better to image
the right kidney through the liver than through
the thick muscles of the back. In this case the
liver is the acoustic window.
Without echoes; echo-free. For example, normal
urine and bile are anechogenic, i.e. they have
no internal echoes.
A feature appearing in an ultrasound image
that does not correspond to or represent an
actual anatomical or pathological structure,
either in shape, direction or distance. For
example, reverberations (q.v.) are artefacts.
Some artefacts may be helpful in interpreting
the image, but others can be very misleading.
The decrease in the intensity of the ultrasound
waves as they pass through tissues, measured
in decibels per centimetre. Attenuation results
from absorption, reflection, scattering and
beam divergence. In most tissues the
attenuation increases approximately linearly
with the frequency of the ultrasound.
xi
xli Glossary
Axial scan
Back wall effect
Beam, acoustic
Boundary
Coronal plane
Coupling agent
Cyst
Debris
Doppler effect
Enhancement,
acoustic
Focusing
Frequency
Gain
See Transverse scan.
A bright echo from the back wall of a cyst.
resulting from the low attenuation of the beam
by the fluid in the cyst and reflection of the
beam by the curved back wall.
See Acoustic beam.
The line at the periphery of two tissues which
propagate ultrasound differently. defined by
the zone of echoes at the interface.
A plane running through the body along the
long axis (from head to toe) at right angles to
the median plane. To scan in this plane. the
transducer is placed on the side of the body
pointing across to the other side and is moved
parallel to the length of the body. A coronal
scan may be obtained with the patient supine.
prone. erect or lying on one side.
A liqUid or gel used to fill the gap between the
skin and the ultrasound transducer. so that
there is no intervening air to interfere with
ultrasound transmission.
A fluid-filled structure (mass) with thin walls.
A simple cyst characteristically has
anechogenic (echo-free) content. with strong
back wall reflections and enhancement of the
echoes behind the cyst. A cyst can be
histologically benign or malignant.
Echogenic solid masses (of various sizes and
shapes. with irregular outlines) within a fluid-
filled mass. May be mobile. changing with the
patient's position or movement.
The change in apparent frequency of a wave as
a result of relative motion between the observer
and the source. The change in frequency is
proportional to the speed of motion.
See Acoustic enhancement.
Adjustment of the ultrasound beam so that it
converges at a particular depth. in order to
improve resolution. Focusing may be electronic
or by a lens attached to the transducer.
The number of complete ultrasound waves
produced each second: for diagnostic
ultrasound this is expressed in megahertz.
1 megahertz (MHz) = 10
6
Hz = 10
6
waves per
second.
Amplification of the reflected ultrasound waves
by the ultrasound unit. The echoes that come
from deep tissues need more amplification
than those that come from more superficial
coronal section
Hyperechogenic
(hyperechoic)
Hypoechogenic
(hypoechoic)
Image reversal
Impedance, acoustic
Interference pattern
Internal echoes
Lens effect
Longitudinal scan
(sagittal scan)
Mass, complex
(mixed mass)
tissues, and thus ultrasound units have
separate gain controls. The "near gain" control
amplifies echoes returning from tissues above
the focal point ofthe beam, while the "far gain"
control amplifies echoes returning from tissues
beyond the focal point of the beam. These
controls can be adjusted to allow proper
comparison of echogenicity at different levels.
Describes tissues that create brighter echoes
than adjacent tissues, e.g. bone, perirenal fat,
the wall of the gallbladder, and a cirrhotic liver
(compared with normal liver).
Describes tissues that create dimmer echoes
than adjacent tissues, e.g. lymph nodes, some
tumours and fluid. It is important to note that
fluid is not the only hypoechogenic material.
Incorrect orientation of the image, i. e. the left
side of the image is shown on the right side of
the monitor or the pOSitions of the head and
feet are reversed. This can be corrected by
turning the transducer through 180
0
or, with
some units, electronically. Image reversal is
sometimes used to mean a background change,
1. e. areas of the image that are normally black
are shown as white. This type of image reversal
can be corrected electronically.
See Acoustic impedance.
Distortion of ultrasound echoes by reflections
from other tissues or by the sum of wavelets
from adjacent reflectors in a scattering medium,
such as liver parenchyma. The result is an
artefactual image superimposed on the normal
pattern. Such interference can usually be
avoided by scanning at different angles.
Ultrasound reflections from tissues of different
density within an organ. Internal echoes may
arise from, for example, gallstones within the
gallbladder or debris within an abscess.
Narrowing ofthe ultrasound beam as it passes
through certain tissues. The lens effect may
sometimes cause a split image.
A vertical scan along the long axis of the body.
"Sagittal" is usually used to refer to a midline
scan, especially in the brain. The landmarks of
the midline longitudinal scan include the nose,
symphysis pubis and spine. When the scan
does not pass through the midline, it may be
called "parasagittal". "Longitudinal" is more
often used to refer to scans of the abdomen or
neck. A longitudinal scan may be obtained
with the patient supine, prone, erect or lying
on one side.
A mass that includes both solid and fluid
areas. It will be shown on ultrasound scans as
Glossary xiii
longitudinal section
xiv Glossary
Mirror effect
Phantom
Reflection
Reverberation
Sagittal scan
Scanning plane
Scattering
having both echogenic and anechogenic
areas; the image will have both non-
homogeneous echoes and echo-free spaces
(hyper- and hypoechogenic patterns).
Reflection of all, or nearly all, the ultrasound
waves by some tissues or tissue interfaces, e.g.
the diaphragm/lung interface. The mirror effect
sometimes produces a mirror-image artefact,
apparently duplicating the image.
A device used for testing and calibrating
ultrasound equipment. It has the same range
of densities as body tissues. The phantom
"tissue" usually contains string and other
objects of known reflectivity in known locations.
Change in direction of the ultrasound waves at
a tissue interface such that the beam does not
enter the second tissue. Also known as echo.
See also Specular reflector.
Reflection of ultrasound waves back and forth
between two strongly reflective surfaces that
are parallel or nearly parallel. When this occurs,
the echoes are delayed in their return to the
transducer, and the resulting image may appear
deeper than the surfaces actually are. It may
also result in duplication, or even triplication,
of the image. For example, reverberations may
be seen in the anterior part of a distended
bladder, or between parallel muscles in the
abdominal wall (see page 37).
See Longitudinal scan.
The section of tissue through which the
ultrasound beam is passing during the scan,
and which will appear on the image.
Reflection and refraction of ultrasound in many
directions at once. This is caused by reflectors
whose width is smaller than the wavelength of
the ultrasound. Only a small fraction of the
transmitted energy is returned to the
transducer.
Shadowing. acoustic See Acoustic shadowing.
Solid Describes tissue that does not include fluid or
empty spaces, e.g. solid tumour, liver, muscle,
or renal cortex. There will be multiple internal
echoes and moderate attenuation of the
ultrasound beam.
Specular reflector Reflective tissue that is smooth and large in
comparison with the ultrasound wavelength,
e. g. the walls of vessels or tissue membranes.
Depending on the angle at which the ultrasound
beam meets the reflector, it can reflect all or
part of the beam.
Transducer
Transverse scan
(axial scan)
Wavelength
Window, acoustic
The part of the ultrasound unit that comes into
contact with the patient. It converts electrical
energy into ultrasound waves. which pass
through the patient's tissues; it also receives
the reflected waves and changes them again
into electrical energy. A transducer is often
called a probe and is connected to the
ultrasound scanner (generator and monitor)
by a flexible cable. Transducers are expensive
and fragile. and must be handled very carefully.
An ultrasound scan at right angles to the long
axis of the body . "Axial" is usually used to refer
to scans of the brain. and "transverse" to scans
of the abdomen or neck. The beam may be
perpendicular or slightly angled to the head or
feet of the patient. A transverse scan may be
obtained with the patient supine. prone. erect
or lying on one side.
The length of a single cycle of the ultrasound
wave. It is inversely proportional to the
frequency and determines the resolution of the
scanner.
See Acoustic window.
Glossary xv
transverse section
Coronal section Neonatal coronal section
Longitudinal (sagittal) section Neonatal sagittal (longitudinal) section
Transverse section Neonatal axial (transverse) section
xvi
Notes
CHAPTER 1
Basics of ultrasound
What is ultrasound? 3
Ultrasound generators 3
Different modes of ultrasound 4
Doppler ultrasound 6
Wave propagation 9
Focusing 10
Attenuation 11
Amplification 11
Boundaries 12
Transducers (scanning probes) 14
Basics of ultrasound 3
What is ultrasound?
Ultrasound is the name given to high-frequency sound waves, over
20000 cycles per second (20 kHz). These waves, inaudible to humans,
can be transmitted in beams and are used to scan the tissues ofthe body.
Ultrasound pulses of the type
produced by the scanners described
here are of a frequency from 2 to
10 MHz (1 MHz is 1 000000 cycles
per second). The duration of the
pulse is about 1 microsecond (a
millionth of a second) and the pulses
are repeated about 1000 times per
second. Different tissues alter the
waves in different ways: some reflect
directly while others scatter the
waves before they return to the
transducer as echoes. The waves
pass through the tissues at differen t
speeds (for example, 1540 metres
per second through soft tissues).
audible sound CVV'cr'-rVVvc'cA g
ultrasound 'V\fV\, '\fV\!\' 'VVIf1J 'V\,n.j\, 'V\fV\, 2-10 MHz
The frequency of ultrasound is many
times greater than that of audible sound.
The reflected ultrasound pulses detected by the transducer need to be
amplified in the scanner. The echoes that come from deep within the
body are more attenuated than those from the more superficial parts,
and therefore require more amplification. Ultrasound scanners have
controls that can alter the overall sensitivity, the "threshold", of the
instrument, as well as change the amplification of the echoes from
different depths. When working with
any scanner it is necessary to achieve
a balanced image, one that contains
echoes of approximately equal
strengths from all depths of tissue.
When the echoes return to the
transducer, it is possible to
reconstruct a two-dimensional map
of all the tissues that have been in
the beams. The information is stored
in a computer and displayed on a
video (television) monitor. Strong
echoes are said to be of "high
intensity" and appear as brighter
dots on the screen.
00
00
monitor
This manual refers only to
ultrasound used for medical
diagnosis, and not to ultrasound
used for other purposes: these
require quite different equipment.
high-frequency pulses
patient
Ultrasound generators
The ultrasound waves are generated by a piezoelectric transducer which
is capable of changing electrical signals into mechanical (ultrasound)
waves. The same transducer can also receive the reflected ultrasound
and change it back into electrical Signals. Transducers are both
transmitters and receivers of ultrasound.
o
o
4 Basics of ultrasound
Different modes of ultrasound
The various modes show the returning echoes in different ways.
1. A-mode. With this type of ultrasound unit,
the echoes are shown as peaks, and the
distances between the various structures
can be measured (Fig. 1a). This pattern is
not usually displayed but similar information
is used to build the two-dimensional
B-mode image.
depth ~
t
strength
of echo
Fig. 1 a. A-mode scan: the position of the peaks shows the depth of the reflecting structure. The
height indicates the strength of the echoes.
2. B-mode. This type of image shows all the
tissue traversed by the ultrasound scan.
The images are two-dimensional and are
known as B-mode images or B-mode sections
(Fig. 1b). If multiple B-mode images are
watched in rapid sequence, they become
real-time images.
. .....
.
...
.- --.
. .
: ....... ..
.. ..
... .
. .. .
*. .*
.... -...
Fig. 1 b. B-mode scan: the echoes are seen as bright dots which show the position of the
reflecting structure on a two-dimensional image.
3. Real-time. This mode displays motion by showing the images ofthe
part of the body under the transducer as it is being scanned. The
images change with each movement of the transducer or if any part
of the body is moving (for example, a moving fetus or pulsating
artery). The movement is shown on the monitor in real time, as it
occurs. In most real-time units, it is possible to "freeze" the
displayed image, holding it stationary so that it can be studied and
measured if necessary.
4. M-mode is another way of displaying motion. The result is a wavy
line. This mode is most commonly used for cardiac ultrasound
(Fig. Ic).
patient's
skin
transducer
/
~ ~ t i m e
moving
structure
depth
Fig. 1c. M-mode scan: the movement of a part of the body, such as the fetal heart, is shown as
a function of time.
Fig. 1 d. M-mode scan of the aorta.
Doppler ultrasound
The electronic circuits for Doppler ultrasound are not included in the
general purpose ultrasound specifications. They can be obtained as an
inexpensive separate unit, but before deciding to do so, read this section
and consider whether the purchase can be justified by the number of
patients with treatable vascular disease who are likely to benefit.
Do you need Doppler? Read and consider carefully.
Is the expense justified?
The Doppler effect
When ultrasound is transmitted towards a stationary reflector, the
reflected waves (echoes) will be of the same frequency as those originally
transmitted. However. if the reflector is moving towards the transmitter.
the reflected frequency will be higher than the transmitted frequency.
Conversely. if the reflector is moving away from the transmitter. the
reflected frequency will be lower than the transmitted frequency.
stationary
moving closer
moving away
The difference between the transmitted and received frequencies is
proportional to the speed with which the reflector is moving away from
or approaching the transmitter. This phenomenon is called the Doppler
effect and the difference between the frequencies is called the Doppler
shift.
I
Movement towards the transducer increases the
reflected frequency.
Clinical applications of a Doppler unit
Although an inexpensive Doppler unit can be used to detect fetal heart
motion, it is seen better by real-time ultrasound. Doppler can be used
to demonstrate blood flow in the peripheral vessels of adults, but in
many countries, the number of patients requiring this examination will
be relatively few and the additional expense cannot be justified as part
of a general purpose ultrasound unit.
The Doppler effect makes it possible to detect and measure the rate of
movement of any fluid such as blood. In blood, the moving reflectors are
the red blood cells. To measure this movement there are two basic types
of Doppler ultrasound unit, the continuous wave (eW) and the pulse
wave (PW).
1. In a continuous wave Doppler unit, the ultrasound is continuous
and the unit measures high velocities accurately, but there is no
depth resolution so that all the movement along the ultrasound
beam is shown together.
2. In a pulsed wave Doppler unit, the ultrasound is transmitted in
pulses of ultrasound into the body, with good depth resolution. It
can be aimed directly to measure the speed of the blood in a
particular vessel (Fig. 2a). The disadvantage is that it cannot
measure high blood velocities in deep vessels and high velocities
may be wrongly displayed as low velocities (aliasing) (Fig. 2b).
Fig. 2a. Pulsed Doppler scan showing the flow of blood just above the bifurcation of the aorta.
Fig. 2b. Doppler aliasing: the peak of each wave is shown below the line at the bottom,
indicating negative flow. These aliasing artefacts occur when the pulse repetition rate of the unit
is not sufficiently high to measure the high velocity of the reflecting structure.
3. In a colour Doppler unit (a further development on the above
principle). the distribution and direction of the flowing blood are
shown as a two-dimensional image in which the velocities are
distinguished by different colours.
4. In a duplex Doppler system, a blood vessel is located by B-mode
ultrasound imaging and then the blood flow is measured by Doppler
ultrasound. This combination of a B-mode and Doppler system
allows the Doppler beam to be directed more accurately at any
particular blood vessel (Fig. 2c,d).
Fig. 2c. Duplex Doppler image of the internal carotid artery. On the left is the Doppler shift
spectrum indicating pulsatile flow towards the transducer. If the flow was away from the
transducer, the spectrum would be upside down. The line is wavy, because the blood velocity
changes during the heart cycle. On the right is a B-mode image showing where the blood flow is
being recorded.
Fig. 2d. If the scanning angle is not correct, the result can be misleading. This is the common
carotid artery of the patient shown in Fig. 2c, but scanned at an angle of nearly 90. As a result,
the flow appears disturbed. while it was, in fact. quite normal. The angle is wrong, not the blood
flow.
Wave propagation
Wave propagation describes the transmission and spread of ultrasound
waves to different tissues. The differences in the ways in which ultrasound
interacts with tissues influence the design of an ultrasound unit, affect
the interpretation ofthe images and impose limitations on the usefulness
of the method.
Ultrasound waves propagate as longitudinal waves in soft tissues. The
molecules vibrate and deliver energy to each other so that ultrasound
energy propagates through the body. The average propagation speed for
soft tissues is 1540 metres per second.
Wavelength
soft tissues
1540 m/s
D)))))8))))))))
bone
4620 m/s
The wavelength of ultrasound is inversely proportional to its frequency.
The higher the frequency, the shorter the wavelength. For example,
ultrasound of3 MHz has a wavelength of 0.5 mm in soft tissue, whereas
ultrasound of 6 MHz has a wavelength of 0.25 mm. The shorter the
wavelength, the better the resolution, giving a clearer image and more
details on the screen. However, wavelength also affects the way in which
the waves go through the tissues (see "Attenuation", p. 11).
wavelength
0.5mm
I
~ ~ / )))))))))) ))))))))))) ))))))J))))) ))))))J) 3MHz
wavelength
0.25 mm
I I
----.....---.. 1-------"-1))))))))))))))))))))))))))))))))))) )))J))) 6 MHz
Focusing
Ultrasound waves can be focused either by lenses and mirrors or
electronically in composite transducers. In the same way that a thin
beam of light shows an object more clearly than a widely scattered,
unfocused beam, so with focused ultrasound: a narrow beam images a
thin section of tissue and thus gives better detail. For best results it is
necessary to focus at the depth in the body that is of most relevance to
the particular clinical problem. For general purpose scanners this
usually means using different transducers for different purposes and
adjusting the focal zone on the unit as necessary (Fig. 3).
Unfocused
beam
Fig. 3. The centre of this image is in focus, while the periphery is not.
Variable focus
Narrow,
focused
beam
Many transducers have a fixed focus. Composite transducers, such as
a linear and convex array, and annular sector transducers (see
pp. 14-15) have an electronically variable focal length which can be
adjusted to the required depth. However, most transducers have a fIxed
focal distance in at least one plane: only annular array sector transducers
have an adjustable electronic focus in all planes. Well adjusted focusing
provides a narrow acoustic beam and a thinner image section: this gives
better resolution of details and a clearer picture with more information.
Attenuation
Tissues in the body absorb and scatter
ultrasound in different ways. Higher frequencies
are more readily absorbed and scattered
(attenuated) than lower frequencies. Thus, to
reach deeper tissues, it is necessary to use lower
frequencies becallse the waves are less likely to
be diverted as they traverse intervening
structures. In practice, it is better to use about
3.5 MHz for deep scanning in adults and 5 MHz
or higher if available for scanning the thinner
bodies of children. 5 MHz or greater is also best
for scanning superficial organs in adults.
Higher frequency shows more
details but is less penetrating.
Amplification
The echoes that return from deeper structures
are not as strong as those that come from
tissues nearer the surface; they must, therefore,
be amplified and in the ultrasound unit this is
done by the time-gain-compensation (TGC)
amplifier. In all ultrasound units it is possible to
vary the degree of amplification to compensate
for ultrasound attenuation in any part of the
body and improve the quality of the final image
(Fig. 4).
adult
3.5 MHz
~
5 MHz
:::s

~
S

~
~
~
~
High frequencies ~ Low frequencies
~ b
have better ~ penetrate etter
resolution but ~ but have less
less depth. ~ resolution.
Fig. 4. On the left the far gain is too low and no echoes have returned from the deeper tissues.
On the right the gain has been corrected and the returning echoes are of equal strength
throughout.
Boundaries
Ultrasound may be reflected or refracted (bent) when it meets the
boundary between two different types of tissue: reflection means the
waves are thrown back and refraction means they change in direction
and are not necessarily reflected (see also p. 13 and p. 27).
reflection refraction
Tissues vary greatly in their effect on ultrasound. For example, the
skeleton and gas in the bowel or chest behave very differently from soft
tissue. When ultrasound waves meet bone or gas in the body, they are
significantly reflected and refracted. Thus, it is usually impossible to use
ultrasound effectively when there is a lot of gas in the bowel: when
examining the pelvis the urinary bladder should be as full as possible
to lift the intestine out of the way. Because of the effect of air, the normal
lungs cannot be examined at all by ultrasound, but pleural fluid or a
mass in contact with the chest wall can be imaged.
The skeleton reflects ultrasound so strongly that the architecture within
a bone or heavily calcified tissue cannot be seen and there is an acoustic
shadow behind it. As a result, imaging through an adult skull or other
bones is not possible (Fig. 5) (see p. 35).
Fig. 5. Two transverse scans through a fetus. showing shadows caused by the fetal spine.
Similar shadows below ribs may obscure parts of the kidneys or liver. Changing the angle of a
scan will alter the position of a shadow so that underlying tissues can be seen clearly
(see p. 28).
A fraction of the incident wave (1) is reflected (2)
at an angle equal to the angle of incidence.
Another fraction (3) passes across the interface
and is refracted, continuing at an angle that is
different from the angle of incidence. The greater
the difference between the characteristic acoustic
impedances, the greater the fraction which is
reflected. The greater the ratio of the propagation
speeds, the greater the refraction. In practice,
this is most important when the incident angle
is zero and the ultrasound wave strikes the
interface perpendicularly.
If the reflecting boundary is much wider than
the wavelength (e.g. 10 or 20 times wider), it acts
like a mirror and is called a specular reflector.
The fetal skull, the diaphragm, the walls of
vessels and the connective tissues are examples
of specular reflectors (Fig. 6).
Ultrasound waves scatter when the width of the
reflectors (scatterers) is smaller than the
wavelength of the ultrasound. Only a small
fraction of the ultrasound wave is scattered
back in the original direction.
The liver and the kidney parenchyma are
examples of scattering media.
scatterers
incident
wave
scattered waves
Fig. 6. Sagittal liver scan: there is strong (specular) reflection from the diaphragm, which is
such a strong reflector that the image of the liver is repeated behind it. The ultrasound waves
travel across the liver first at transmission, again after being reflected from the diaphragm, then
again from the tissue interfaces.
It is because of boundary effects that a coupling
agent must be used for scanning, to prevent air
trapped between the skin and the transducer
acting as a barrier to the ultrasound waves.
Transducers (scanning probes)
The transducer is the most expensive part of any ultrasound unit. The
probe contains one or more transducers that transmit the ultrasound
pulses and receive back the echoes during scanning. Each transducer
is focused at a particular depth. The beam of ultrasound emitted varies
in shape and size depending on the type of transducer and the generator.
Mechanical
transducers
Convex
(curvilinear)
transducer
Linear array
transducer
b
e
I II I I II II II
a
I II I I II I
c
Phased array
sector
transducer
II I
tr ansducers
d
housing
/"
~
annular
array
transducers
The shape of the scans from different transducers
1. Linear array. Scans from this type of transducer are rectangular.
They are most useful in obstetrics and for scanning the breast and
the thyroid (Fig. 7a).
Fig. 7a. The rectangular image from a linear array transducer.
2. Sector scanner. These scans are fan-shaped, almost triangular,
and originate through a very small acoustic window. These scanners
can be used whenever there is only a small space available for
scanning. They are most useful in the upper abdomen and for
gynaecological and cardiological examinations (Fig. 7b).
Fig. 7b. The fan-shaped image from a sector transducer.
3. Convex transducer. This produces a scan somewhere between
those of the linear and the sector scanners and is therefore useful
for all parts of the body except for specialized echo cardiography
Fig. 7c).
Fig. 7c. The wide fan-shaped image with a broad, curved apex from a convex transducer.
Basics of ultrasound -15
- -----------
CHAPTER 2
Choosing an ultrasound
scanner
The monitor 18
The scanner 18
Servicing the scanner 18
What controls are needed on the scanner? 18
Recording the image 19
Choosing the appropriate transducer 20
What is needed in the ultrasound scanning room? 21
What electrical outlets are needed? 21
When the scanner is delivered 22
18 Choosing an ultrasound scanner
Choose a scanner that will perform the examinations needed at your
hospital; there is no justification for buying accessories or gadgets that
are not likely to be used very often. The scanner should at least match
the specifications given in the Annex (p. 321). Apart from the technical
specifications, there are some basic rules to be observed when choosing
a scanner.
13 cm (about 5 inches)
minimum
The monitor
The monitor (viewing screen) should be at least
13 em x 10 em (or about 16 em diagonally).
The scanner
1. The scanner should be portable and light
enough to be carried by hand for 100 metres.
2. The scanner must be suitable for use in the
local climate, i.e. protected from dust or
capable of being used in high or low
temperatures, as appropriate.
3. The scanner must be tough enough to
withstand adverse transport and storage
conditions. It should not be damaged by
movement in an aircraft or in a vehicle on
rough roads.
4. The scanner must operate satisfactorily from
the power supply in the hospital or clinic
where it is going to be used. This requirement
should be checked and double-checked
before the scanner is accepted. The unit
should be compatible with local voltage and
frequency, and it should be able to stabilize
fluctuations in supply.
Servicing the scanner
10cm 1
a b o ~ t ~ inches)
minimum
[ g
Servicing must be available within a reasonable distance. It may be wise
to purchase a unit similar to other scanners in use in the area, so that
sufficient expertise and spare parts are available.
What controls are needed on the scanner?
The scanner must be equipped with a video monitor (TV screen) and to
control the images there must be:
1. An overa11 sensitivity control to alter the amount of information on
the video screen.
2. Separate controls to alter the surface (near) echoes and the deep
(distant) echoes. These are known as near gain and far gain controls.
3. A control (frame freeze) to hold the image on the screen so that it can
be viewed for as long as necessary.
./
16 em
/
voltage?
frequency?
stable?
stabilizer
sensitivity [Q
near gain far gain
frame freeze 1m
(hold the image) ~
Choosing an ultrasound scanner 19
4. A control to measure the distance between two pOints shown on the
image. This should be done electronically and usually means
positioning a small dot at each end of the length to be measured. The
distance between the dots should be shown automatically in
centimetres or millimetres on the screen. Biometric tables (for
obstetrics) are an advantage.
Recording the image
It should be possible to add patient identification and other data to the
image electronically: it is very desirable that a permanent record of
important scans be put in the patient's medical record. There are several
ways to do this. varying in cost and efficiency.
1. The best and most expensive method is to
record the image on an X-ray film. This
requires an image-processing unit and a
special camera. It may be necessary to have
a darkroom. Ordinary X-ray film can be
used but the best results are obtained using
Single-emulsion X-ray film, which is
expensive. Prints on paper are less expensive
but not always of the same quality (see item
3, below).
2. The next best method is also expensive: it
requires a self-processing camera and film
specifically designed to be attached to the
ultrasound unit. Both the camera and the
films are expensive and films are not always
readily available. However, the results are
good and the prints can be seen almost
immediately.
3. There are image-recording units that will
print the image on special paper (thiS is
much less expensive than using film). The
images are quite satisfactory for routine
records, but the paper must be protected
from excessive heat and light.
4. The image on the screen can be
photographed on black and white film using
most 35 mm reflex cameras. An additional
close-up lens may be necessary. The film
will then have to be processed and printed
in the usual way. This can take time,
espeCially in a rural hospital.
5. If it is not possible to purchase any type of
recording unit, exact details of the findings
and relevant measurements must be noted
in the patient's record at the time of the
scan.
+ .. ........ +
5cm
I 1
2 3 4 ~
Name
Date
00
00
patient data
o
o
Choosing the appropriate transducer
The best transducer for general work is a convex transducer of 3.5 MHz
focused at 7-9 cm. If this type of transducer is not available then both
linear and sector transducers of 3.5 MHz will be necessary. If children
or thin adults are to be scanned, an additional 5.0 MHz transducer
focused at 5-7 cm is helpful.
1. Obstetric ultrasound. If most of the
ultrasound examinations will be for general
obstetrics, the transducer should be linear
or convex, either 3.5 or 5.0 MHz focused at
7-9 cm. If only one transducer can be
purchased, choose 3.5 MHz. The 5 MHz
transducer is best during early pregnancy:
the 3.5 MHz is better in later pregnancy.
Obstetric
linear convex
3.5 or 5 MHz
7-9 cm focus depth
General purpose
sector convex
~ or V
3.5 MHz
7-9 cm focus depth
2. General purpose ultrasound. If the
examinations will include the upper
abdomen of adults and the pelvis, as well
as obstetrics, a sector or convex transducer
of 3.5 MHz focused at 7-9 cm is most
suitable.
Paediatric
linear sector
~
7.5 MHz
5.0 MHz
3. Paediatric ultrasound. For children a
5.0 MHz transducer with a focus of about
5-7 cm is needed. If neonatal brain scans
are to be carried out, a sector transducer of
7.5 MHz focused at 4-5 cm will be required
(and can be helpful for adult testis and
neck).
5-7 cm focus depth
4-5 cm focus depth
(for neonatal brain scan,
adult testis and neck)
Summary
Best choice Second choice
linear sector
and
For children
linear
3.5 MHz
3.5 MHz 5.0 MHz
7-9 cm focus depth
The complete ultrasound unit
power
source
7-9 cm focus depth 5-7 cm focus depth
g
/ monitor
o gener,lorlreceiver
~ I ~ = = : : S : = ~ = scanner
/ tranSducer
patient
What is needed in the ultrasound scanning room?
I . -
No radiation protection is needed.
'I
There is no dangerous radiation from a medical
diagnostic ultrasound machine and walls of any
material are satisfactory. However, the room
must be kept dry and free from dust.
The room must be big enough to accommodate
the scanner, a couch, a chair and a small table
or desk. It should be large enough to allow a
trolley to be wheeled in and the patient to be
transferred to the couch. There must be a door
to ensure privacy.
The couch should be finn but soft, and it should
be possible to lift one end so that the patient can
recline comfortably. If the couch is on wheels
there must be good brakes. Two firm pillows
should be available. The couch should be easy
to clean.
There should be facilities for washing hands and
providingdIinking-water, preferably in the room,
and there should be a toilet nearby.
There must be a window or some other form of
ventilation and adequate lighting, preferably
with a dimmer switch or some other way of
varying the brightness of the lights. Bright
sunlight should be screened or curtained off. If
the room is too bright, it will not be easy to see
the images on the video screen.
What electrical outlets are needed?
o
o
No special electrical power supply is required: a standard wall outlet is
all that is usually necessary, for example, 220 V at 5 A or 110 V at
lOA. No special electrical connection is needed but the exact specillcations
of the equipment should be verified with the supplier. Itis important that
the ultrasound unit to be purchased is suitable for use with the available
electrical supply and the company that sells the equipment should be
required to check and confirm this in writing.
The main electrical supply to many hospitals or clinics, particularly in
the developing world, is very variable in both voltage and frequency. If
there is too much fluctuation, the ultrasound unit may be damaged or,
at the very least, function poorly. It may be necessary to buy a good
voltage stabilizer. This should be determined before the equipment is
purchased.
g
I

:::: ~ s
220 V
(110 V)
gJ
220 V
(110 V)
voltage
stabilizer
When the scanner is delivered
It is important to check every aspect of the scanner before the person
who delivers the equipment has left. Whatever is happening, take time
to do this because once he or she has gone, it may be too late!
Every new ultrasound unit must be supplied with a detailed user's
manual and a service manual, either separate or combined. Make sure
that they are there when the unit is delivered and are complete,
particularly if supplied in a loose-leaf binder.
Open the user's manual and look at the instructions. Go through them,
checking the controls one by one as described in the manual: make sure
you can follow the instructions. user's
manual
service
manual
-
It is not sufficient to watch the supplier demonstrate the unit
upon delivery.
Try all the controls and every aspect of the equipment for yourself.
Use the following as a checklist:
1. Confirm that the plugs provided will fit into the
outlets of the electrical supply.
2. Confirm that the voltage setting for the unit is
compatible with the electrical supply.
3. Turn on the unit and make sure there is no
interference on the screen. (If the electrical
supply also powers an air-conditioner, surgical
diathermy, a faulty fluorescent-tube starter or
other electrical equipment, artefacts may
appear on the screen.) Test the unit on a
patient or colleague. Check all the controls
individually.
4. The operation of all transducers and their
cables can be tested by slowly moving a pencil.
lubricated with coupling agent. along the
transducer surface. The image should not
disappear from the monitor while the pencil is
in contact with any part of the transducer in
any pOSition. (Repeat this examination with
the transducer above. alongside and under the
pencil or test object.) Make sure that movement
of the cable which connects the transducer to
the ultrasound unit does not cause any blurring.
loss of clarity or change in the image (see
opposite).
110 V
1111 1 CO (0
IIII coco
110 V
co
CD
5. A sector transducer can be tested by scanning a hypodermic needle
through the side or bottom of a beaker full of water. The image of the
needle should not move if the needle is kept still. needl e
coupling
agent
6. Bending the cable while the transducer is
held in position should not cause any
change. and certainly no movement or
blurring. of the image.
7. Check any electronic method of measuring length and make sure
the electronic pointers are clearly seen on the screen and that
distances can be easily read.
/'
8. If the unit is provided with automatic biometric or measurement
tables. try out all of them to make sure the stored data are readily
accessible and easily read.

9. All biometric measurements or tables that are programmed into the
unit should be tested to make sure that all the data specified are
actually available on the equipment.
10. Check that the service and maintenance
manual is available and complete.
11. Receive and check a fully completed and
dated written guarantee (warranty).
12. Withhold the final payment for the
equipment until it has been used for one
month and is working satisfactOrily .
/'
K ' "1"11/11111"11111
"
I, nlU, jlijllliU
. ultrasoundbyscanning normal people (this is quite
manual beside you. With' time and, 'practice, you
., .' 1 . _, --" .. ,:". . _ _ _. _ " '
:.: to, recogn ize on the video screen ,thenorr:nal ' images
.' "-11 ... '", ""'-. -:." ,. ' . ,
allthe'analomicallandr,narks.
. .. '-... 1 ,.::
l
24
Notes
CHAPTER 3
Basic rules of scanning
Orientation of the image 26
Background of the image 27
Acoustic enhancement and shadowing 28
Frequency and resolution 29
Focus of the ultrasound beam 29
Sensitivity and gain 30
Artefacts 32
Quality control 40
26 Basic rules of scanning
Orientation of the image
It is possible for the images on the monitor to be
reversed so that, on transverse scans, the left
side of the patient is seen on the right side of the
screen. Although there may be an indicator on
the transducer, itis essential before scanning to
check visually which side of the transducer
produces which side of the image. This is best
done by putting a finger at one end of the
transducer and seeing where it appears on the
screen. If incorrect, rotate the transducer 180
0
and check again (Fig. 8a). On longitudinal scans,
the head ofthe patient should be on the left side
and the feet on the right side of the screen.
Fig. 8a. A finger on the transducer should
produce an image on the same side of the
screen. If the image is on the wrong side,
rotate the transducer by 180
0

Contact with the patient's skin
00
00
The transducer must be moved across the
patient; therefore, the patient's skin in the
region to be examined must always be amply
covered with a coupling agent (see pp. 44-45) to
allow transmission of the ultrasound beam and
easy movement of the transducer.
While the transducer is moved slowly across the
patient it must always be kept in close contact
with the skin through the coupling agent;
movement must be continuous and gradual
while the operator carefully watches the image
on the screen.
Incorrect
00
00
Correct
transducer
o
o
Fig. 8b. Two axial
images of the same
fetal head, but
aligned 180
0
differently. When
starting to scan, the
images on the
screen must be
tested as shown in
Fig. Sa.
transducer
coupling agent
Close contact
skin
,
I
,

.... -----
,...---..,: - - -,
,
Basic rules of scanning 27
Background of the image
The image on the screen may be predominantly black or predominantly
white. It may have a white background with black echoes (Fig. 9 upper),
or a black background with white echoes showing as spots or lines
(Fig. 9 lower). There is usually a switch to make this change; if not, an
engineer should adjust the machine so that it always shows a black
background with white echoes (Fig. 9 lower).
Fig. 9. Transverse images of
an enlarged uterus with the
background changed.
black echoes on white
background (incorrect)
white echoes on black
background (correct)
Distribution of the ultrasound beam
Bladder
Body tissues reflect ultrasound in two different ways. Some tissues act
like mirrors, sending the waves directly back. Others scatter the waves
in the way fog scatters a beam of light. For example, the diaphragm is
a "mirror", known technically as a "specular reflector". The monitor will
show a clear and exact image that corresponds well with the position and
the shape of the diaphragm. The liver, however, scatters ultrasound
waves and the pOSition of the dots shown on the screen does not exactly
correspond with any particular detail in the liver. This is an "interference
pattern" resulting from waves being scattered in different directions. In
either case, the use of a black background with white echoes permits
better differentiation.
scattered
The liver scatters
ultrasound like
fog scatters light.
This creates an
"interference
pattern."
The diaphragm acts
like a mirror and
sends ultrasound
back. This is a
"specular reflector."
reflected
Acoustic enhancement and shadowing
Clear liquids allow ultrasound to pass directly through
without much alteration, so that echoes that come from
tissue behind liquid are usually enhanced (brighter). This is
known as "acoustic enhancement" (Fig. lOa). Drinking enough
water to fill the stomach will displace gas-filled bowel, providing
an acoustic window. This is particularly useful in visualizing
the body and tail of the pancreas.
Gas in the bowel or elsewhere can present a variety of
sonographic patterns. The beam can be scattered, reflected,
absorbed. and refracted, making it very difficult to image
underlying structures. For this reason, ultrasound cannot be
used to image the nonnal lungs or to demonstrate lung
disease other than peripheral masses. A chest X-ray provides
much better infonnation.
Dense materials such as bones or calculi (stones) cast
shadows on structures behind them, because the ultrasound
waves do not go through them. This is known as "acoustic
shadowing". For example, ribs may obstruct the field of view
so the structures behind must be examined obliquely through
the intercostal spaces (Fig. lOb, c) (see also p. 35).
Fig. 10a. A liquid-filled structure. the gallbladder, with posterior enhancement due to
low ultrasound attenuation. The walls of the gallbladder cause two lateral shadows.
Fig. 10b. When the liver and ascites are imaged through the ribs, the ribs cast two
shadows and there is a layer of reverberation in the ascites (see also p. 37).
Fig.10c. Imaging the same patient at an angle through the intercostal space
eliminates the rib shadows and the reverberation.
pancreas
Frequency and resolution
The higher the frequency of the ultrasound. the better the resolution.
This means that smaller details become visible when higher frequency
is used. However. the penetration of the ultrasound into the body will be
less. Scanning is. therefore. a compromise and the highest frequency
that is also sufficient to penetrate deeply enough should always be used
(Fig. 11) (see also p. 9 and 11).
5 MHz 3.5 MHz 5 MHz 3.5 MHz
Focus of the ultrasound beam
,
Fig. 11. Images of a uterus
made at different scanner
frequencies. Quality is best
judged by comparing the
details of the endometrium.
There is reverberation in the
liquid-filled urinary bladder.
Because the organs or
parts of the body that
are of interest will be
at different depths. the
focus of the transdu-
cer should ideally be
adjustable (pp. 10 and
20). If the focal dis-
tance is fixed. the most
suitable transducer
must be chosen for the
particular exam ina -
tion. The best choice
is described in each
section ofthe manual.
, ' ,
---+--- ---4!--
6
'"
'"
'I'
Correct
" ; . '\:,'
: .
Incorrect ::.,
','
. "
Fig. 12. The focus is correct on the left, showing details of the yolk sac; on the right there are
no details because the focus is set too deep.
Sensitivity and gain
It is important to know that the wrong (gain)
setting can make diagnosis inaccurate or even impossible.
Fig. 13 shows the effect of varying the sensitivity and gain controls.
Fig. 13a. Liver ultrasound. Left: low far gain. Right: low near gain.
Fig. 13b. Liver ultrasound. Left: high overall gain. Right: low overall gain.
Fig. 13c. Liver ultrasound. Left: low midfield gain. Right: correct gain.
--- -------- -------- --- - ---
Fig. 13d. Fetal skull. Left: the overall sensitivity is too high. Right: the overall sensitivity is now
correct but too high for accurate measurement of the biparietal diameter.
Fig. 13e. The overall sensitivity is now too low for general scanning, but correct for the
measurement of the biparietal diameter.
Fig. 13f. Left: poor definition because the near gain is too high; compare the indistinct image of
the upper part of the skull with the much clearer lower half (compare Fig. 13d and e; see also
p. 33). Right: the gain has been overcorrected; the near gain is now too low and the far gain is
too high.
. . .
If the image is poor even when the gain has been changed,
apply more coupling agent.
Artefacts
An artefact is an additional. missing or distorted image which does not
conform to the real image of the part being examined. Artefacts do not
arise from the primary ultrasound beam, or direct echoes from the part
being scanned, but result from distortion or attenuation of the image.
There are many different causes. Recognition of such artefacts is
important because they can be misleading and may even be mistaken
for some important finding that may affect the diagnosis. Other artefacts
may provide important additional information and should be recognized
and used.
Cysts
A cyst usually appears as an echo-free area and
the structures behind the cyst are enhanced:
there are no echoes from within cysts because
there are no impedance interfaces within the
liquid. Because the liquid does not absorb
ultrasound to the same extent as tissue, the
echoes from behind the cyst are over-
compensated by the equipment and appear
enhanced-the strong back wall effect
(Fig. 14a, b).
A cyst is seen as an echo-free area
with a strong back wall. If there are
echoes within a cyst, these may be
real or artefactual.
Fig. 14a. A liquid-filled cyst in the liver: there are no internal echoes and there is a strong back
wall effect.
Fig. 14b. This ovarian cyst has thick walls and contains debris. This causes echoes within the
cyst, which will probably alter when the patient is scanned in a different position (see pp. 34-35).
transducer
patient
..r'n" .. "..,' .... cyst
strong
back wall
Fig. 14c. Longitudinal scan: the gain is incorrectly adjusted, so that the outline of the kidney
and the periphery of the liver are not well seen.
Fig. 14d. Longitudinal scan with proper gain: the margins of the kidney and the internal details
of the kidney and liver are now well defined.
Near and far gain must also be carefully adjusted (Fig. 14e-t).
Fig. 14e. Images of the fetal head.
Left: balanced image of low sensitivity.
Right: near gain too high; it must be
reduced while the overall gain is
increased to obtain a good image of
the whole head.
Fig. 14f. Left: a well balanced
image. Right: far gain too high, near
gain too low; the far gain must be
reduced and the near gain
increased.
A space. such as a cyst filled with clear fluid. appears to be free of echoes
on the screen. The walls of the cyst reflect the ultrasound at an angle so
that infonnation does not return to the transducer. This results in
acoustic shadows laterally. but behind the cystic area the echoes will be
enhanced (the strong back wall) (Fig. 15).
Fig. 15a. A hepatic cyst: the internal fluid is clear. and there are no echoes. The walls of the
cyst reflect the ultrasound away from the transducer, causing lateral shadows.
Fig. 15b. Blighted ova: two liquid-filled spaces showing posterior enhancement and lateral
shadowing.
Artefacts may be seen in any cystic structure (such as the urinary
bladder or gallbladder) and tend to be seen anteriorly. becoming less
intense with depth. They may disappear or change in character as the
transducer is moved. However. real structures in a cyst. such as septa.
maintain their relationships regardless of the pOSition of the transducer.
True echoes can be due to reflection from blood clot. pus or necrotic
debris. and these tend to be at the bottom of the cyst: ifnot attached to
the wall, they will move when the patient changes pOSition (Fig. 16).
Fig 16a. Malignant ovarian cyst: a large cyst with an internal septum, which did not alter when
the patient was scanned in different positions.
Debris within a cyst may float, forming a level which will vary as the
patient's position changes (Fig. 16b, c).
Fig. 16b. A cyst with a strong back wall, lateral shadows and internal debris.
Fig. 16c. The same patient as in Fig. 16b scanned in a different position. The floating debris
has moved.
Shadows
Bone, calculi and calcification result in an acoustic shadow. Ultrasound
cannot pass through bone unless it is very thin (e.g., the skull of a
neonate). In order to see what is behind, a different angle of scanning
must be used (Fig. 17a, b).
Fig. 17a. A large acoustic shadow below a calculus in the gallbladder.
Fig. 17b. This image of a kidney is partly obscured by the shadow of a rib. Scanning in different
phases of respiration may move the kidney out of the shadow.
Abdominal wall
Significant subcutaneous fat and muscle can scatter ultrasound,
making the images of deeper structures less distinct. Sometimes the
muscles cause a double ultrasound image giving a false impression of
separation: an incorrect diagnosis (e.g. of twins) may result. Always
use multiple projections at different angles to confirm any suspected
abnormality (Fig. 18).
Fig. 18. Muscles, especially the abdominal muscles, can act as convex lenses. This early
pregnancy looks like a twin pregnancy because the lens effect of the rectus muscle causes the
borders of the gestational sac to be imaged twice. On a longitudinal scan the "twin" could not be
found.
Gas
Gas reflects ultrasound and obscures the tissues behind it through
refraction and shadowing. Intestinal gas can obscure the liver, pancreas,
para-aortic lymph nodes, uterus and ovaries. Sometimes it is easy to
move the gas in the bowel: for example, if the urinary bladder is full, the
uterus and the ovaries are nearly always easily seen because the bowel
is pushed upwards out of the field of view. In other cases, oblique,
lateral, or posterior scans with the patient sitting or standing may be
necessary (Fig. 19).
Fig. 19. The image obtained during inspiration (left) shows
all of the gallbladder, but during expiration (right) more than
half the gallbladder is obscured by bowel gas.
suggested scanning
positions when gas
obscures tissues
Reverberation
Reverberation occurs when the ultrasound beam passes from one tissue
to another with a very different acoustic impedance. e.g. from intestinal
gas to liver or ribs: the reverberation can obscure tissues that lie behind
the gas (Fig. 20a) .
Reverberations can completely change the image. producing either
parallel lines or a mirror image. For example. reverberations between
parallel layers of tissue below the skin may be seen as parallel lines in
the urinary bladder (Fig. 20c).
,
.
.
,
Uterus
"
. ... - ---"
/
. uterus ..
. --
"
Fig. 20a. Gas artefacts. Left:
there are repeated images of
the liver behind the
diaphragm; these are
artefactual. caused by air in
the lungs. Right:
characteristic intestinal gas
artefacts below the
gallbladder might be
interpreted as body
structures.
Fig. 20b. Reverberations: the
lines are caused by multiple
reflections of the gas between
the bubble and the body
surface. Gas artefacts can
obscure underlying structures
by absorption, oblique
reflection and refraction.
Fig. 20c. When the uterus is
scanned through a full urinary
bladder, the parallel layers in
the abdominal wall may
cause reverberation, seen as
anterior echoes in the
otherwise echo-free bladder.
The transverse scan (left)
looks different from the
longitudinal scan (right)
because of the different
position of the transducer.
Fig. 20d. Shadowing and
reverberation of ultrasound
waves in the subcutaneous
layers of this fetal head give
false impressions of defects
in the skull.
Incomplete imaging
Artefacts due to incomplete imaging are a source of error. since only that
part of the tissue or any object that is actually in the acoustic beam will
be imaged. Thus. in pregnancy. only part of a fetal bone may appear on
the image because the remainder is not within the beam. As a result.
the bone may appear to be incomplete or shorter than it really is
(Fig. 21a. b) .
Fig. 21a. An incompletely imaged bone.
Fig. 21 b. The same bone now fully imaged.
In practice. the most important artefact of this type occurs when needle
biopsy or aspiration is guided by ultrasound. Whenever the tip of the
needle is not within the scanning plane. it will not be seen on the screen.
and the image will give the impression of a much shorter needle
(Fig. 21c) (see also Chapter 22. p.317).
Fig. 21 c. Images of a needle in a water bath. On the left. the needle is not entirely in the
scanning plane and therefore appears shorter than it really is (the cross indicates the actual
depth). On the right. the whole needle is imaged.
"' ... , ....... ........ ,4.
Fig, 22. Imaging the same body structure from different positions and transducer angles, Left:
only the upper pole of the kidney is well seen. Right: the upper pole is blurred, but the rest of
the kidney is seen clearly.
If you cannot see what is needed, turn the patient over on each side: or turn the
pathmt half over (oblique); or examine while the patient is standing or on hands
and knees.
oblique
- - - ~
decubitus
erect
prone
hands and
knees
Quality control
Every ultrasound unit should be checked every day before clinical use.
Although some basic quality control is essential. thorough and reliable
quality control requires complex electronic and physical instrumentation.
Only a trained physicist can do this properly and it is not usually
practical outside a major department. However. simple quality control
is not difficult and should be done regularly.
Ultrasound grey scale commercial "phantoms" allow regular checking of
the resolution and sensitivity of the ultrasound unit and such checks
should be made at least every three months and preferably more often.
I
Each machine must be checked, particularly when
it is first delivered (see p. 22).
Ultrasound machines can vary in quality over a
period of use.
Phantom
1. With good quality scans, it should be possible
to demonstrate the cavum septi pellucidi in
a 35-week-old fetus (Fig. 23) (see p. 247).
When no phantom is available. this can be
used as a clinical test to show that the
scanner is working properly. The test should
be carried out every three months.
maternal
abdomen
section
plane
fetal head
Fig. 23a. With any scanner, it should be possible to see the cavum septi pellucidi in the head of
a 35-week fetus.
Fig. 23b. With a high quality scanner the cavum can be identified at a much earlier age.
2. The superior mesenteric artery should be visible as a round or oval
hole close to the pancreas of a normal adult (Fig. 24). The easiest way
to test the machine consistently is to image your own mesenteric
artery. Keep a scan after each test for comparison.
Fig. 24. Transverse scan: the superior mesenteric artery is shown as a round hole surrounded
by echogenic fat, close to the pancreas.
3. Hepatic veins as small as 3 mm in diameter should be visible when
scanned at 45 to the surface of a normal liver (Fig. 25).
Fig. 25. A good quality scanner should demonstrate 3 mm veins in the liver. This should be
used as one of the regular tests of image quality.
4. In a normal adult, the liver parenchyma should be slightly brighter
than the nearby renal cortex (Fig. 26).
Fig. 26. Longitudinal scan through the liver and the right kidney: the normal liver parenchyma is
more reflective than the normal kidney parenchyma. This is another useful way to check image
quality.
Check the quality of yourscanner at least every three
months.Your patients deserve consistently accurate
results.Keeprecordsof all tests.
.2
Notes
CHAPTER 4
Acoustic coupling agents
Introduction 44
Ingredients 45
Preparation 45
44 Acoustic coupling agents
Introduction
If, during an ultrasound examination, air
becomes trapped between the transducer and
the skin of the patient, it will form a barrier that
reflects almost all the ultrasound waves,
preventing them from penetrating the patient.
To obtain a good image, a fluid medium is
needed to provide a link between the transducer
and the surface of the patient. This fluid is called
an acoustic coupling agent, often referred to as
"gel".
Water is not a good coupling agent because it
evaporates rapidly owing to the heat of the body:
it also runs away over the patient as the
transducer is moved. It should only be used in
an emergency, when nothing else is available.
Oil, either mineral or vegetable, is a good coupling
agent, but when used for a long time may
dissolve the rubber or plastic shielding of the
equipment. If oil gets on the operator's fingers,
as it inevitably will, it might damage the controls
of the ultrasound unit.
The best acoustic coupling agent is a water-
soluble gel. Many are ommercially available, but they are usually
expen ive and sometimes difficult to obtain. It is not necessary to use a
particular coupling agent with specified eqUipment. even though
manufacturers often suggest that this 1s essential . Special coupling
agents do not give a better image. The formula for a general purpose
coupling ag nt for use with any transducer is given on p. 45.
The coupling agent is best applied using a squeeze bottle, from which it
can be squirted onto the patient's skin. This avoids contamination. Any
refillable plastic squeeze bottle is SUitable, but it must be completely
clean and dry before it is filled with the coupling agent. If there is an open
wound, a skin rash or any other risk of infection, cover the transducer
(or the skin) with thin plastic; put coupling agent on both sides of the
plastic. The transducer must be cleaned after every patient.
The coupling agent should be removed with
paper tissues, paper or cloth towels. It must be
completely removed to avoid soiling the patient's
clothing.
There can never be too much coupling agent.
skin
/
clean the skin
Ingredients
Almost any hospital or commercial pharmacy should be able to prepare
a suitable gel. All are based on synthetic resins, polymers of acrylic acid
or other liquids that become water-soluble when neutralized with an
appropriate alkalizing agent.
1. Carbomer. A synthetic high molecular weight polymer of acrylic
acid cross-linked with allylsucrose and containing 56-68% of
carboxylic acid groups. It is a white, fluffY, acidic, hygroscopic
powder with a slight characteristic odour.
Neutralized with alkali hydroxides or amines, it is very soluble in
water, alcohol and glycerol.
There are three carbomers: the most suitable is carbomer 940,
which forms a clear gel in aqueous and non-aqueous vehicles. If
carbomer 940 is not available, carbomer 934 or 941 can be used.
However, they may not be quite so easy to mix (as described below)
as carbomer 940.
2. EDTA (edetic acid). A white crystalline powder, very slightly soluble
in water. Soluble in solutions of alkali hydroXides.
3. Propylene glycol. A colourless, odourless. viscous hygroscopic
liquid with a slight sweet taste. Density = 1.035-1.037 g/ml.
4. Trolamine (triethanolamine). A mixture of bases containing not
less than 80% of triethanolamine, with diethanolamine and small
amounts of ethanolamine. A clear, colourless or slightly yellow,
odourless, viscous hygroscopic liquid. Density = 1.12-1.13 g/ml.
Formula
The gel is prepared using these ingredients in the following amounts:
Carbomer
EDTA
Propylene glycol
Trolamine
Distilled water
Preparation
10.0 g
0.25g
75.0 g (72.4 ml)
12.5 g (11.2 ml)
up to 500 g (500 ml)
1. Combine the EDTA with 400 g (400 ml) of water, making sure that
it is dissolved, then add the propylene glycol.
2. Add the carbomer to the above solution and stir vigorously, if
possible with a high speed stirrer, taking care to avoid the formation
of indispersible lumps.
3. Wait until the mixture forms a gel and no more bubbles are
observed.
4. Mix the trolamine with the remaining water and add the mixture to
the gel to make a total of 500 g.
5. Stir carefully; do not shake, to prevent the formation of air bubbles
in the gel.
The recommended formula is not known to irritate healthy skin or stain
clothing, and is easy to clean off.
This gel may become more liquid when the patient is sweating, because
it is affected by a high concentration of salts. This can be avoided by
cleaning and drying the skin before applying the gel. If left in direct
Acoustic coupling agents 45
46 Acoustic coupling agents
sunlight, the gel may liquefY. It is incompatible with bivalent or trivalent
cations, such as calcium, magnesium and aluminium; if prolonged
storage is likely, it is wise to store the gel in the dark. The stability of
carbomer is considerably influenced by the pH, which must be maintained
between 5 and 10. Outside these limits, the viscosity will fall.
CHAPTER 5
Abdomen
Indications 49
Preparation 49
Scanning technique 51
Indications
When the clinical symptoms indicate a particular organ, refer to the
appropriate section. e.g. liver. spleen. aorta, pancreas. kidney. etc.
Indications for general abdominal scans:
1. Localized abdominal pain with indefinite clinical features.
2. Suspected intra-abdominal abscess. Pyrexia of unknown origin.
3. Nonspecific abdominal mass.
4. Suspected intra-abdominal fluid (ascites).
5. Abdominal trauma.
Preparation
1. Preparation of the patient. The patient should take nothing by
mouth for 8 hours preceding the examination. If fluid is essential to
prevent dehydration. only water should be given. If the symptoms
are acute. proceed with the examination. Infants-clinical condition
permitting-should be given nothing by mouth for 3 hours preceding
the examination.
As the examination progresses. and ifthere
is no clinical contraindication, it may be
helpful to give the patient water to drink,
especially when scanning the pancreas. the
lower abdomen and pelvis (see p. 113 and
p.196).
2. Position ofthe patient. The patient should
lie comfortably on his/her back (supine).
The head may rest on a small pillow and. if
there is much abdominal tenderness, a
pillow may also be placed under the
patient's knees.
Cover the abdomen with coupling agent.
The patient can be allowed to breathe qUietly,
but when a specific organ is to be examined.
the patient should hold the breath in.
3. Choice of transducer. Use a 3.5 MHz
transducer for adults. Use a 5 MHz
transducer for children or for thin adults.
Curvilinear or sector transducers are
preferable when available.
3.5 MHz
adults
5 MHz
children
Abdomen 49
50 Abdomen
4. Setting the correct gain. Start by placing
the transducer centrally at the top of the
abdomen (the xiphoid angle) and ask the
patient to take a deep breath and hold it in.
Angle the transducer beam towards the
right side of the patient to image the liver.
Adjust the gain setting so that the image has
normal homogeneity and texture. It should
be possible to recognize the strongly
reflecting lines of the diaphragm next to the
posterior part of the liver (Fig. 27a).
The portal and hepatic veins should be
visible as tubular structures with an echo-
free lumen. The borders of the portal veins
will have bright echoes. but the hepatic
veins will not have such bright borders
(Fig. 27b).
Fig. 27a. Longitudinal scan: the normal liver and diaphragm.
Fig. 27b. Longitudinal scan: hepatic and portal veins.
Fig. 27c. Transverse scan of a normal liver.
angle
transducer
patient
breathes in
patient
holds breath in
Scanning technique
Mter adjusting the gain. slowly move the
transducer from the midline across the
abdomen to the right. stopping to check the
image approximately every 1 cm. Repeat at
different levels. When the right side has been
scanned, examine the left side in the same way.
The transducer can be angled in different
directions during this process to provide more
information and better localization. It is
important to scan the whole abdomen: if, after
angling the beam, the upper parts of the liver
or spleen are not seen. scanning between the
ribs may be necessary.
After these transverse scans, turn the
transducer 90 and start again centrally at the
xiphoid angle below the ribs. Again, locate the
liver and, if necessary, ask the patient to take
a very deep breath to show it more clearly.
Make sure that the gain settings are correct.
When necessary, angle the transducer towards
the patient's head (cephalad). Scan between
the ribs to visualize better the liver and the
spleen.
Below the ribs, keep the transducer in a vertical
position, and move it downwards towards the
feet (caudad). Repeat in different vertical planes
to scan the whole abdomen.
If any part of the abdomen is not well seen with
the transducer, the patient may be scanned
while sitting or standing erect. If necessary,
scan in the lateral decubitus position: this is
particularly useful for imaging the kidney or
spleen. Do not hesitate to turn the patient.
Whenever there is any suspected abnormality,
use the technique described in the appropriate
section.
It is important to recognize:
1. Aorta and inferior vena cava.
2. Liver, portal vein, hepatic vein.
3. Biliary tract and gallbladder.
4. Spleen.
5. Pancreas.
6. Kidneys.
7. Diaphragm.
8. Urinary bladder (if filled).
9. Pelvic contents.
If any pathology is suspected during the
abdominal scanning, refer to the appropriate
section of this manual.
patient breathes
in deeply and
holds breath in
. ,
: '
U-
"
: ,
:,
.,
"
y : ~
y . . ,
\y
Abdomen 51
M
:
,
/ i ""
, "-
.... )--
...... )-
~ ..... . )-
.r< ...... )--
~ ...... )-
:.: ...... )--
1< :>-
j< . )-
f ')--
angle transducer
towards patient's head
~ ;
, . .
" .
,.
"
,:
,.
"
, :
I : .
:: : y
, . . y
tv
52
Notes
CHAPTER 6
Abdominal aorta
Indications 54
Preparation 54
Normal abdominal aorta 56
Aortic displacement 57
Aneurysm 58
Aortic dissection 60
Narrowing of the aorta 61
Aortic prosthesis 62
Idiopathic aortitis 63
54 Abdominal aorta
Indications
1. Pulsatile abdominal mass.
2. Pain in the midline of the abdomen.
3. Poor circulation in the legs.
4. Recent abdominal trauma.
5. Suspected idiopathic aortitis (patient under the age of 40 with
vascular symptoms relevant to the aorta or major branches).
Preparation
mouth for 8 hours preceding the examination. If fluid is desirable,
only water should be given. Ifthe symptoms are acute, proceed with
the examination. Infants-clinical condition permitting-should be
given nothing by mouth for 3 hours preceding the examination.
2. Position of the patient. The patient should
lie comfortably on his/her back (supine).
The head may rest on a small pillow and, if
there is much abdominal tenderness, a
pillow may also be placed under the
patient's knees.
Apply coupling agent down the midline of
the abdomen over a width of 15 cm from
below the ribs to the pubic symphysis.
Scanning is best performed with the patient
holding the breath in, but he/she may
breathe quietly until a specific region needs
more careful examination.
transducer for children or thin adults.
V ?
3.5 MHz
adults
5 MHz
children
abdomen (the xiphoid angle).
Angle the beam to the right side of the
patient to image the liver; adjust the gain to
obtain the best image (see p. 50). r
~ \ ~ \
angle
transducer
Scanning technique
Move the transducer back to the midline and
move it slowly towards the left until a pulsatile
tubular structure is located. Follow this
downwards to below the umbilicus, where the
structure can be seen to divide: this is the
bifurcation of the aorta (Fig. 28a, b).
Use transverse imaging to measure the cross-
sectional diameter ofthe aorta at various levels.
Image the iliac arteries by angling slightly to the
right or left just below the bifurcation of the
aorta.
patient breathes in
umbilicus
patient holds breath in
transducer
Whenever a localized irregularity or variation is seen in the aorta
(Fig. 28c), scan transversely at that level and closely above and below it.
In elderly patients, the course of the aorta may vary and there can be
some displacement or change in direction, but the diameter of the aorta
should not change significantly. If the aorta cannot be identified, scan
through the back towards the left kidney.
Gas
If there is intervening bowel gas, apply gentle
pressure and angle the transducer; use an oblique
or lateral projection if necessary, and scan from
either side of the spine. Occasionally an erect
scan may be used to displace gas-filled bowel.
Fig. 28a. Longitudinal scan: a normal aorta.
Fig. 28b. Coronal scan: the lower aorta, aortic bifurcation.
oblique
Fig. 28c. Longitudinal scan: the irregular aorta of an elderly patient.
decubitus
Abdominal aorta 55
56 Abdominal aorta
Normal abdominal aorta
The nonnal cross-sectional diameter ofthe adult aorta, measured as the
maximum internal diameter, varies from about 3 cm at the xiphoid to
about 1 cm at the bifurcation. Transverse and vertical diameters should
be the same.
Measurements should be taken at various points down the length of the
aorta. Any significant increase in diameter caudally (towards the feet) is
abnonnal (Fig. 29).
Upper ~ ......... ~ -@ 2-3 em
~
~
1.5-2.5 em
~
Middle ~ ...... .
Lower
-@
1-2 em
Iliac
spine
--T--

1 em or less
Fig. 29a. Transverse scan: the upper abdominal aorta and the coeliac axis.
Fig. 29b. Transverse scan: the mid-abdominal aorta and the superior mesenteric artery.
Fig. 29c. Transverse scan: the aorta at the level of the bifurcation.
(j)
c+J

*
Aortic displacement
The aorta may be displaced by scoliosis, a
retroperitoneal mass or by para -aortic lymph
nodes; in some patients these can mimic an
aneurysm. Careful transverse scans will be
needed to identifY the pulsating aorta: lymph
nodes or other extra-aortic masses will be seen
posteriorly or surrounding the aorta (Fig. 30).
Fig. 30a. Longitudinal scan: the abdominal aorta is displaced by enlarged lymph nodes.
Fig. 30b. Transverse scan: the abdominal aorta is almost surrounded by enlarged lymph nodes.
of the aorta is more than 5 cm in
referral for clinical assessment is
:required.There is a high risk that an aorta of this size
reo
Abdominal aorta 57
58 Abdominal aorta
Aneurysm
A significant increase in the diameter of the aorta as it descends caudally
(towards the pelvis) is abnormal; also, any section of the aorta that has
a diameter greater than normal is likely to be aneurysmally dilated.
However, aneurysm must be distinguished from dissection (p. 60), and,
in elderly patients, marked tortuosity may be misleading. An aneurysm
may be focal or diffuse, symmetrical or asymmetrical (Fig. 31a, b).
Internal reflections may be due to a clot (thrombus) which may cause
local narrowing of the lumen (Fig. 3Ic). When there is a thrombus,
measurements must include both the thrombus and the echo-free
lumen. It is also important to measure the length of the abnormal
section (see also Aortic dissection, p. 60, and Idiopathic aortitis, p. 63).
A "horseshoe kidney" or a mass, e.g. lymph nodes, may also be mistaken
clinically for a pulsating aneurysm. A horseshoe kidney will be anechoic
and will appear to pulsate because it lies across the aorta. Transverse
and, if necessary, angled scans should distinguish the aorta from the
renal tissue.
The cross-section of the aorta should not exceed
3 cm at any level. If the diameter is more than
5 cm, or if any aneurysm is increasing rapidly in
size (a change in diameter of 1 cm per year is
regarded as rapid), there is a significant
probability of rupture.
If a fluid collection is seen in the region of an aortic
aneurysm and the patient complains of pain, the
condition is serious. Leakage may have occurred.
Fig. 31a. Transverse scan: a symmetrical aneurysm of the abdominal aorta.
Fig. 31 b. Transverse scan: an asymmetrical aneurysm of the abdominal aorta with thrombus in
the lumen.
Fig. 31c. Longitudinal (upper) and transverse (lower) scans of an aortic aneurysm: the lumen is
narrowed by a thrombus.
Abdominal aorta 59
60 Abdominal aorta
Aortic dissection
The aorta may dissect at any level (Fig. 32a) and over a short or long
section. Dissection occurs most commonly in the thoracic aorta. which
is difficult to image With ultrasound. The image of a dissection may
suggest a double aorta or double lumen (Fig. 32b). The presence of intra-
luminal clot (thrombus) can also be very misleading because the lumen
Will then be narrowed (Fig. 3Ic. p. 59).
Whenever there is a change in aortic diameter. either enlargement or
narrowing. dissection should be suspected. Longitudinal and transverse
scans are essential to display the full length of the dissections; oblique
scans are also necessary to show clearly the full extent.
When an aortic aneurysm or dissection is diagnosed, the renal arteries
must be located prior to surgery to see whether they are involved
(Fig. 32c). If possible. the state of the iliac arteries should also be
demonstrated (see also pp. 56-59).
The clinical recognition of a highly pulsatile mass in the midline
of the abdomen is an indication for an ultrasound scan.
Fig. 32a. Longitudinal scan: an aortic dissection.
Fig. 32b. Transverse scan: the aorta appears to be double because of dissection.
Fig. 32c. Transverse scan: dissection of the abdominal aorta at the level of the renal arteries.
Narrowing of the aorta
Any localized narrowing of the aorta is significant and should be
visualized and measured in both diameters, with both longitudinal and
transverse scans to show the extent of the narrowing.
Atheromatous calcification should be assessed throughout the length of
the aorta. Whenever possible, the aorta should be traced past the
bifurcation into the left and right iliac arteries, which should also be
examined for narrowing or widening (Fig. 33a, b) (see p. 56 for normal
measurements) .
In elderly patients, the aorta may be tortuous or narrowed because of
arteriosclerosis, which may be focal or diffuse. Calcification ofthe aortic
wall will produce focal areas of acousti shadowing on the scan. A
thrombus may develop. especially at the bifurcation of the aorta.
followed by occlusion of the vessel. Doppler ultrasound or aortography
(contrast radiography) may be necessary. Each part of the aorta should
be examined before stenosis or dilatation is diagnosed.
Fig. 33a. Longitudinal scan: stenosis of the abdominal aorta due to thrombosis close to a
partially calcified atheromatous plaque.
Fig. 33b. Longitudinal scan: the tortuous aorta of an elderly patient.
Abdominal aorta 61
62 Abdominal aorta
Aortic prosthesis
When the patient has had surgical repair of the aorta, it is important to
assess the position and calibre of the prosthesis and, using transverse
sections, to exclude dissections or leakage. Fluid adjacent to a recently
inserted graft may be due to haemorrhage, but can also be due to
localized post -surgical oedema or infection. Correlation with the clinical
condition of the patient and follow-up ultrasound scans are essential.
In all cases the full length of the prosthesis must be examined, together
with the aorta above and below it (Fig. 34).
Fig. 34a. Longitudinal scan: an aorta with an intraluminal prosthesis.
Fig. 34b. Transverse (upper) and longitudinal (lower) scans of an aneurysm of the aorta with a
surgically placed prosthesis.
Fig. 34c. Transverse scan: an aorta with an infected prosthesis, which has resulted in an
abscess. Blood leaking from an aneurysm would have the same appearance.
Idiopathic aortitis
The aneurysms of idiopathic aortitis occur most commonly in women
under the age of 35 years but are sometimes seen in children. Aortitis
may affect any part of the descending aorta and may cause tubular
dilatation, asymmetrical dilatation or stenosis. Scanning in the renal
area is essential to assess the patency of the renal arteries. In patients
with aortitis, rescanning every six months is required, since an area of
stenosis may subsequently dilate and become an aneurysm. Because
ultrasound cannot image the thoracic aorta, aortography is needed to
show the full extent of the aorta, from the aortic valve to the bifurcation
and to demonstrate all the major aortic branches (Fig. 35).
Fig. 35a. Longitudinal scans: Idiopathic aortitis in an 11-year-old girl. The upper abdominal
aorta is dilated and irregular (upper), but becomes smoother and of normal diameter in the mid-
abdominal region (lower).
Fig. 35b. Transverse scan of the same patient showing post-stenotic dilatation of the renal
artery.
Abdominal aorta 63
64
Notes
CHAPTER 7
Inferior vena cava
Indications 66
Preparation 66
Normal inferior vena cava 67
Abnormal vena cava 68
Masses in the inferior vena cava 69
66 Inferior vena cava
Indications
1. Recent onset of dilated veins in the lower legs. with or without
phlebitis (inflammation).
Varicose veins are not an indication for caval ultrasound.
2. Multiple or suspected pulmonary emboli.
3. Renal tumour.
Preparation
prevent dehydration. only water should be given. If the symptoms
are acute. proceed with the examination.
2. Position of the patient. The patient should lie comfortably on his
or her back (supine) with the head on a pillow. If necessary. a pillow
may be placed under the knees.
Apply coupling agent liberally down the
midline of the abdomen over a width of
15 cm from below the ribs to the pubic
symphysis.
3. Choice of transducer. For adults use a
3.5 MHz curvilinear transducer. Use a
5 MHz transducer for children or thin adults.
obtain the best image (see p. 50).
Scanning technique
The patient is normally scanned while holding a
deep breath in. or breathing gently. The breath
should be held whenever any suspected
abnormality is imaged.
Scanning is normally longitudinal and
transverse. If bowel gas prevents adequate
imaging. oblique or lateral scans may be
necessary to obtain a better image. Scanning
with the patient erect may also be helpful.
Longitudinal scans will demonstrate the length
and diameter of the inferior vena cava. which
will be shown as a tubular. fluid-filled structure
to the right of the aorta. Transverse scans will
show the diameter at different levels.
15 cm
patient breathes in
Start by placing the transducer centrally at the top oftbe abdomen (the
xiphOid angle). Angle the transducer to the right until the vena cava is
seen along the right side of the spine.
When the patient takes a deep breath and holds it in. the vena cava will
distend and be seen more clearly. Then re-examine the vena cava during
active breathing: the wall of the vessel is thin. smooth and less dense
than that of the neighbouring aorta. The vena cava appears in high
contrast to the surrounding tissues.
r y
3.5 MHz 5 MHz
adults children
~ .. \
angle
transducer
~
(
\ j
: ::
~ ::
. "
*t
,
,
Normal inferior vena cava
Duling respiration there should be change in the diameter of the vena
cava, which normally collapses duling inspiration and expands duling
expiration: this change allows recognition and differentiates the vena
cava from the aorta. In transverse scans, the cross-section of the infelior
vena cava is flattened or oval, whereas the aorta is round (Fig. 36a). The
infelior vena cava will be flatter during inspiration and more oval during
expiration, particularly forced expiration (the Valsalva manoeuvre)
(Fig. 36b).
Once the vena cava has been recognized, careful scanning will usually
show the hepatic and renal veins, and sometimes the iliac veins.
In elderly patients, the aorta may occasionally push the vena cava to the
light or even lie in front it. Rarely. there may be two vena cava, one on
either side of the aorta: these can be mistaken for hypoechogenic,
enlarged lymph nodes. The variation in the size of each vena cava on
respiration will help distinguish the veins from such solid tissues.
Fig. 36a. Transverse scan: the inferior vena cava and aorta.
Fig. 36b. Longitudinal scans: there is flattening of the inferior vena cava during inspiration (left)
compared with expiration (right).
Fig. 36c. Transverse scan: the inferior vena cava and the hepatic veins.
Inferior vena cava 67
68 Inferior vena cava
Abnormal vena cava
Dilatation of the vena cava occurs when there is right-sided cardiac
failure. There is no significant variation in diameter during respiration
and the major caval branches may also dilate (Fig. 37a).
Compression of the inferior vena cava can be caused by hepatic
tumours, enlarged lymph nodes or retroperitoneal fibrosis (Fig. 37b).
Anterior displacement of the vena cava can occur as a result of a spinal
deformity, a spinal abscess (e.g. a tuberculous psoas abscess) (Fig. 37c)
or a retroperitoneal tumour such as a lymphoma (Fig. 37d).
Fig. 37a. Longitudinal scan: dilated inferior vena cava in a patient in right-sided cardiac failure.
Fig. 37b. Longitudinal scan: compression of the inferior vena cava by enlarged lymph nodes.
Fig. 37c. Longitudinal scan: anterior displacement of the inferior vena cava by the spine.
Fig. 37d. Displacement and compression of the inferior vena cava by an adrenal tumour.
Masses in the inferior vena cava
Well defined echogenic structures within the vena cava are probably due
to thrombus or to an extension of a renal tumour (Fig. 38a); always check
the outline of the kidneys when there are echogenic structures within
the vena cava. A large venous channel parallel to the course of the vena
cava may be a dilated ovarian or spermatic vein (Fig. 38b). If there are
bright echogenic reflectors with acoustic shadowing within the vena
cava, the clinical history should be checked to exclude an intraluminal
filter (Fig. 38c).
Whenever thrombosis or tumour is suspected, it is important to examine
the vena cava throughout its length to assess the extent of the lesion
prior to surgery. Invasion of the vena cava occurs in renal cell carcinoma,
hepatoma and adrenal carcinoma (see Chapter 13). Ifthere is doubt, an
inferior vena cavagram, computerized tomography (CT) or magnetic
resonance imaging may be necessary.
Fig. 38a. Coronal scan: tumour tissue filling the inferior vena cava.
Fig. 38b. Coronal scan: thrombosis of the ovarian vein.
Fig. 38c. Longitudinal scan: inferior vena cava blocked by thrombosis in an intraluminal filter.
Inferior vena cava 69
70
Notes
CHAPTER 8
Liver
Indications 72
Preparation 72
Normal liver 74
Abnormal liver 76
Trauma to the liver 89
72 Liver
Indications
1. Enlarged liver/hepatomegaly.
2. Suspected liver abscess.
3. Jaundice (see also pp. 107-109).
4. Abdominal trauma.
5. Ascites.
6 . Suspected metastases in liver.
7 . Suspected liver mass.
8. Right upper abdominal pain.
9. Screening for endemic echinococcosis.
Preparation
1. Preparation of the patient. The patient
should take nothing by mouth for 8 hours
preceding the examination. If fluid is
essential to prevent dehydration, only water
should be given. If the symptoms are acute,
proceed with the examination. Infants-
clinical condition permitting-should be
given nothing by mouth for 3 hours preceding
the examination.
In many patients, additional information
can be obtained from an antero-posterior
supine radiograph of the abdomen. If there
is acute pain, a radiograph should also be
taken with the patient erect and must include
the diaphragm to exclude subphrenic air
from a perforated viscus.
2. Position of the patient.
The patient lies supine.
Apply coupling agent
liberally, first over the right
upper abdomen, then over
the rest ofthe abdomen as
the examination proceeds.
3. Choice of transducer. For
adults use a 3.5 MHz
transducer. For children
or thin adults use a 5 MHz
transducer.
3.5 MHz
adults
5 MHz
children
4. Setting the correct gain. The gain setting
should allow the diaphragm to be clearly
seen; the liver (when normal) should appear
homogeneous throughout its depth
(Fig. 39). It should be possible to see clearly
the normal tubular structures (the portal
veins with bright edges and the hepatic
veins without bright edges, see pp. 73 and
74). Hepatic arteries and bile ducts are not
seen unless dilated.
Before scanning a specific area, ask the
patient to take a deep breath and hold it in.
supine
y
patient breathes in
3 hours
angle
transducer
Fig. 39a. Longitudinal scan of a normal homogeneous liver.
Fig. 39b. Longitudinal scan of the portal and hepatic veins in a normal liver.
Scanning technique
Scanning should be in sagittal, transverse and
oblique planes, including scans through the
intercostal and subcostal spaces.
Scanning should be done with a slow rocking
movement of the transducer in all planes to
obtain the best visualization of the whole liver.
v
v
Intercostal
y
10rotation,
left side down
It is difficult to measure accurately the (Jverall
\ size , of" the liver. In the mid-clavicular line,' the
Igngltudinal measurementfr(lm.the diaphragm
edge of the liverislIsually less]han
14 'em in ' an adult, but there is considerable
variation.
Liver 73

'\;::."" r , .. ,,)?"
", , "
" ..
):.,
t
......
Usually less
than 14 cm
74 Liver
Normal liver
The normal liver parenchyma appears homogeneous, interrupted by the
portal vein and its branches which are seen as linear tubular structures
with reflective walls. The thinner hepatic veins are non-reflective. In a
normal liver, it should be possible to follow the hepatic veins to their
confluence with the inferior vena cava. Hepatic veins can be made to
dilate when the patient performs the Valsalva manoeuvre (forced
expiration against a closed mouth and nose) . The vena cava may be seen
in the liver and may vary with respiration. The aorta may be identified
as a pulsatile tubular structure behind and medial to the liver (Fig. 40).
Fig. 40a. Oblique (upper) and transverse (lower) scans of the liver showing the
portal and hepatic veins and the inferior vena cava.
Fig 40b. Two transverse scans at slightly different angles showing the inferior vena
cava, the hepatic veins and the bright (echogenic) walls of the portal veins.
The falciform ligament will be seen as a hyperechogenic structure just
to the right of the midline in the transverse plane (Fig. 41a).
Fig. 41 a. Transverse scan: the fissure of the ligamentum teres and the falCiform ligament.
As well as the light and left lobes of the liver. it is also important to
recognize the caudate lobe. limited posteriorly by the infelior vena cava
and separated antero-sup riorly from lhe left lobe of the liver by a highly
reHective line. It is limited inferiorly by the proximal left portal vein. The
caudale lobe must be identified because it may be mistaken for a mass
(Fig. 41bJ.
Fig. 41 b. Transverse scan: the caudate lobe of the liver and the fissure of the ligamentum
venosum.
The gallbladder and the right kidney must also be identified. The
gallbladder will appear on a longitudinal scan as an echo-free. pear-
shaped structure (Fig. 41c) (see also p. 94).
Fig. 41 c. Transverse scan: the normal gallbladder.
The pancreas and vertebral column should be identified.
The echogenicity of the normal liver parenchyma lies midway between
that of the pancreas (more echogenic) and the spleen (less echogenic)
(Fig. 41d).
Fig. 41 d. Normal echogenicity of different lobes of the liver.
Liver 75
76 Liver
Abnormal liver
Enlarged liver/hepatomegaly: homogeneous pattern
When the liver is enlarged but has a nonnal diffuse homogeneous echo
pattern, consider the following:
1. Congestive cardiac failure. The hepatic veins will be dilated
(Fig. 42a). The inferior vena cava does not vary on respiration. Look
for a pleural effusion above the diaphragm.
- --_ ....
____ __ _ ~ ~ ----iriie-rior\ena-cava "
Fig. 42a. Longitudinal scan: hepatomegaly, dilated hepatic veins and a right-sided pleural
effusion due to congestive cardiac failure.
2. Acute hepatitis. There are no characteristic sonographic changes,
but the liver may be enlarged and tender. Ultrasound is useful to
exclude other underlying disease and, when the patient is jaundiced,
for differentiating between obstructive and non -obstructive jaundice
(see also pp. 107 and 108). Ultrasound does not usually give further
useful infonnation on hepatitis (Fig. 42b).
Fig. 42b. Transverse scan: oedema of the wall of the gallbladder, but normal hepatic
parenchyma. The patient had acute hepatitis.
3. Tropical hepatomegaly. The only significant finding is liver
enlargement, usually associated with splenomegaly.
4. Schistosomiasis. The liver can be either sonographically nonnal or
enlarged. with thickening ofthe portal vein and the main branches.
which become highly echogenic. especially around the porta hepatis.
The splenic veins may be enlarged and. ifthere is portal hypertension.
there is usually splenomegaly. An increase in collateral circulation
may develop around the splenic hilus and along the medial edge of
the liver. This is seen as tortuous. echo-free. vascular structures
which must be distinguished from fluid-filled bowel. (Continued
imaging will show peristalsis in bowel.) Periportal fibrosis may be
due to either &histosoma mansoni or S. japonicum (Fig. 43) .
Fig. 43a. Transverse scans of left lobe of the liver. showing fibrosis around the portal veins
(periportal fibrosis) due to Schistosoma mansoni.
Fig. 43b. Transverse scan: periportal fibrosis due to Schistosoma mansoni.
Fig. 43c. Scans from two patients showing dilatation of the splenic vein and multiple
varicosities due to portal hypertension.
Liver 77
78 Liver
Enlarged liver: non-homogeneous pattern
1. Without discrete masses. When there is increased echogenicity in
the liver parenchyma, with loss of the highly reflective edges of the
peripheral portal veins. cirrhosis. chronic hepatitis or a fatty liver
should be suspected. Liver biopsy maybe required to establish the
diagnosis. In severe cases, the region of the liver furthest away from
the transducer may nol be clearly imaged, so that the hepatic veins
may not be identified (Fig. 44) .
Fig. 44. Longitudinal scan: a fatty liver.
Cirrhosis is not excluded when an ultrasound scan of
the liver appears normal.
2. With multiple echogenic masses. Multiple masses of various
sizes. shapes and echo textures. producing a non-homogeneous
echo pattern throughout the liver, are consistent with:
Macronodular cirrhosis. The liver is enlarged with echogenic masses
of various sizes but with normal intervening tissue. The normal
vascular anatomy is distorted (Fig. 45a). There is an increased risk
of malignancy. but this can only be diagnosed by biopsy.
Fig. 45a. Macronodular cirrhosis.
Multiple abscesses. These are usually ill defined. with strong
back wall echoes and internal echoes (Fig. 45b) (see pp. 86-87).
Fig. 45b. Transverse scan: multiple hepatic abscesses (amoebic) .
Multiple metastases. These may be hyperechogenic or hypo-
echogenic and well circumscribed or ill defined. or both (Fig. 46).
Metastases are often more numerous and more variable in size
than abscesses; multinodular hepatocarcinoma can resemble
metastases.
Fig. 46a. Transverse scan: multiple well-defined metastases in the liver.
Fig. 46b. Transverse scan: multiple metastases in the liver. some well and others poorly defined.
Lymphoma. This may be considered when there are multiple
hypoechogenic masses in the liver. usually with irregular outlines
and without associated acoustic enhancement. It is not possible
to distinguish between lymphoma and metastases by ultrasound
(Fig. 47).
Fig. 47. Transverse scans: lymphomatous masses in the liver.
Haematomas. These are often irregular in outline. with acoustic
enhancement. However. when blood has clotted. the haematomas
may be hyperechogenic. It is important to obtain a clinical history
of either trauma or anticoagulant medication (see also p. 89).
The differential diagnosis between liver
haematomasis not easily
.. by ultrasound examination alone.
': .. :.:...
. ""','::
Liver 79
80 Liver
Small liver/shrunken liver
A diffusely increased echogenicity and distorted portal and hepatic veins
in a shrunken liver are usually due to micronodular cirrhosis (Fig. 48).
This is often associated with portal hypertension. splenomegaly. ascites.
dilated splenic veins and multiple varices. The portal vein may be
normal or small in the intrahepatic portion. but enlarged in the
extrahepatic portion. If the lumen is filled with echoes. there may be
thrombosis. which can extend into the splenic and mesenteric veins
(Fig. 49). Some patients with this type of cirrhosis may have a liver that
appears normal in the early stages.
Fig. 48. Longitudinal scan: ascites and a small shrunken liver. the result of cirrhosis.
Fig. 49. Transverse scan: thrombosis of the main portal vein.
Cystic lesions in normal or large liver
1. Well defined solitary cyst. A well rounded. echo-free mass with
acoustic enhancement. usually less than 3 cm in diameter. and
often a chance finding without symptoms. is likely to be a solitary
simple congenital cyst. A small hydatid cyst must also be excluded
and cannot always be differentiated sonographically (Fig. 50a) (see
pp.82-83).
Fig. 50a. Transverse scan: a simple hepatic cyst with a sharp outline and acoustic
enhancement.
2. Solitary cyst with a rough irregular outHne. See liver abscess.
p.86.
3. Multiple cystic lesions. Multiple spherical cystic masses of vary-
ing sizes. completely echo-free with a sharp outline and posterior
acoustic enhancement. may indicate congenital polycystic disease
(Fig. 50b). Search for cysts in the kidney. pancreas and spleen;
congenital cystic disease can be very difficult to differentiate from
hydatid disease (see also p. 82).
~ , \
,
,
. ~ . ' Right kidney
Fig. 50b. Longitudinal scan: congenital polycystic disease of the liver.
4. Complex cyst. Haemorrhage or infection of any cyst may result in
internal echoes and resemble an abscess or necrotic tumour
(Fig. 50 c) (see pp. 85-86).
Fig. 50c. Haemorrhage into a cyst. which on ultrasound resembles an abscess or a necrotic
tumour.
Liver 81
82 Liver
5. Echinococcal cyst. Hydatid disease can present a broad spectrum
of sonographic features (Fig. 51).
Fig. 51a. A simple, centrally echo-free intrahepatic cyst with a sharp outline and distal acoustic
enhancement. Because of the host reaction, there is a double wall around this hydatid cyst.
Fig. 51 b. An echo-free mass containing fine internal debris due to hydatid sand. This may float
freely or be at the bottom of the cyst.
Fig. 51c. A well defined cystic mass with internal debris and a membrane floating within the
cyst. This is pathognomonic of a hydatid cyst.
Fig. 51 d. A complex mass containing multiple internal cysts and daughter vesicles, with
echogenic material filling some of the cysts and the intervening spaces. This usually indicates a
viable cyst.
Fig. 51 e. Infected hepatic cysts are difficult to differentiate from abscesses or other masses.
The hazy outline of this cyst indicates the possibility of infection.
Fig. 51f. An echogenic mass with a sharp outline and calcification in the walls. This may
indicate a dead hydatid cyst: hepatomas and liver abscesses seldom calcify (see pp. 85 and 86).
Fig. 51g. A hydatid cyst that has partially collapsed may resemble a scar.
Fig. 51 h. A small collapsed hydatid cyst with calcification in the cyst wall .
. .
... " __' ,',. .. _ .
;.i):.B.efore needle aspiration of ahapparently solitary cyst,
I ,":.' ,
the whole abdomen and X-ray the chest. Hydatid
-..... ar'e usually multiple and may be dangerous to
"- - .' "",. ,.
'. :J3s,:>irate.
Liver 83
84 Liver
Differential diagnosis of liver masses
It may be difficult to distinguish hepatocellular carcinoma from multiple
liver metastases or abscesses. Primary carcinoma usually develops as
one large dominant mass, but there may be multiple masses of various
sizes and patterns, which may have a hypoechogenic rim. The centre
may become necrotic and appear quite cystic, with fluid-filled cavities
and thick, irregular margins. It can be very difficult to distinguish such
tumours from abscesses (Fig. 52) (see also p. 86).
Fig. 52a. Hypoechogenic nodules with irregular outlines: metastases from colon carcinoma.
Fig. 52b. A large nodule in a cirrhotic liver. This is a hepatoma, but could be mistaken for an
abscess.
Fig. 52c. A mass in the liver with a surrounding halo and central necrosis: metastasis from
breast carcinoma.
Fig. 52d. A necrotic metastasis with a central low-level echo, which could easily be mistaken for
an abscess: clinical correlation is essential to make the correct diagnosis.
A single solid mass in the liver
Many different diseases may cause a solitary, solid mass in the liver. The
differential diagnosis may be very difficult and may require biopsy (see
also p. 84). A solitary, well defined hyperechogenic mass close to the liver
capsule may be a haemangioma: 75% of haem angiomas have posterior
acoustic enhancement without acoustic shadowing, but when large
may lose hyperechogenicity and cannot be easily differentiated from a
primary malignant liver tumour. Occasionally there will be multiple
haemangiomas, but they do not usually produce clinical symptoms.
It can be very difficult to differentiate a haemangioma from a solitary
metastasis, abscess, or hydatid cyst. A lack of clinical symptoms
strongly suggests haemangioma. To confirm the diagnosis, either
computerized tomography, angiography, magnetic resonance imaging
or radionuclide scanning with labelled red blood cells will be necessary.
The absence of other cysts helps to exclude hydatid disease. If there has
been internal haemorrhage, the ultrasound images may resemble those
of a necrotic abscess (Fig. 53a, b).
Fig. 53a. Transverse scan: haemangioma of the liver.
Fig. 53b. A large haemangioma of the liver, irregular in outline and hypoechogenic.
A single homogeneous mass with a low-level echo around the periphery
is probably a hepatoma. However, hepatomas may also present with
central necrosis or as a diffuse mass, can be multiple and may also
infiltrate the portal or hepatic vein (Fig. 53c) (see pp. 81 and 84).
Fig. 53c. A solitary hepatoma with a surrounding low-level echo and areas of central necrosis.
Liver 85
86 Liver
Liver abscess
It is very difficult to differentiate between a bacterial abscess, an
amoebic abscess and an infected cyst. All may be either multiple or
single, and usually present as hypoechogenic masses with strong back
walls, irregular outline and internal debris (Fig. 54a). There may be
internal gas (Fig. 54b). Bacterial infection may also occur in an inactive
amoebic abscess or in a healed amoebic abscess cavity. A necrotic
tumour (see p. 84) or a haematoma (see p. 89) can also resemble an
abscess (Fig. 54a, b).
Amoebic abscess
In the early stages an amoebic abscess may be echogenic, with poor edge
definition, or even isodense and not visible. It will later appear as a mass
with irregular walls and with acoustic enhancement. There is usually
internal debris. As the infection progresses, the abscess may become
well demarcated with a sharper outline: the debris may be finer
(Fig. 54c). The same changes occur after successful treatment but the
abscess cavity may remain for several years and be confused with a
cystic mass. The scar of a healed amoebic abscess persists indefinitely
and may eventually calcifY (Fig. 54d).
-,Amoebic abscesses in the liver
'. Usually solitary but may be multiple and of different sizes.
<:! IMorefrequent in the right lobe of the liver.
;- Usually near the diaphragm but can be anywhere.
'::. to metronidazole or other treatment.
., May be isodense and invisible on the first scan. If suspected clinically, repeat
,the scan after 24 and 48 hours.
'.' -.'
;:. ' C':Innotbe reliably from pyogenic abscesses.
Summary: amoebic and bacterial abscesses and hydatid cysts
Internal Clinical Response to
Number Location wall Contents presentation metronidazole
usually usually
with
patient
Amoebic solitary; can right lobe and irregular
debris
moderately yes
abscess be multiple peripheral unwell
multiple
usually
with
patient
yes, if an
Bacterial or
deep
irregular
debris
very ill
anaerobic
abscess solitary infection
multiple
sharp
anechogenic
patient usually
Cyst or anywhere (other than no
solitary
outline
hydatid)
asymptomatic
Fig. 54a. A pyogenic abscess in the liver.
Fig. 54b. A gas-forming hepatic abscess with multiple bright reverberation artefacts.
Fig. 54c. Transverse scan: an early amoebic abscess in the right lobe of the liver,
hypoechogenic and irregular in outline.
Fig. 54d. An amoebic abscess, which has been treated and now forms an almost echo-free
subdiaphragmatic mass next to the right kidney. The walls are sharp and there is no acoustic
enhancement.
Liver 87
88 Liver
Subphrenic and subhepatic abscesses
A predominantly echo-free, sharply delineated, crescentic area between
the liver and the right hemidiaphragm may be due to a right-sided
subphrenic abscess. Subphrenic abscesses are of various sizes and are
often bilateral, so the left subphrenic region should also be scanned. If
the abscess is chronic, the edges become irregular: septa may develop
together with debris visible on ultrasound imaging (Fig. 55).
Fig. 55a. An acute right subphrenic abscess.
Fig. 55b. A chronic subphrenic abscess.
When using ultrasound to search for the cause of pyrexia of unknown
origin, or postsurgical pyrexia, both left and right subphrenic regions
should be examined.
The posterior aspect of the lower chest should also be scanned to
exclude an associated pleural effusion (which can also be caused by
pyogenic or amoebic liver abscess). A chest X-ray may be helpful. If a
subphrenic abscess is found, it is necessary to scan the liver to exclude
an associated amoebic or pyogenic abscess (Fig. 55c).
Fig. 55c. Transverse scan: a right pleural effusion and a pyogenic hepatic abscess.
Occasionally, a subphrenic abscess may extend to the subhepatic
space, most commonly between the liver and the kidney, where it will
show a similar echo pattern-either anechogenic or with complex
echoes from internal debris.
Trauma to the liver
Haematomas
Ultrasound can reliably detect intrahepatic haematpmas. which vary
from hyperechogenic to hypoechogenic. However. the clinical history
and symptoms may be needed to differentiate haematomas from
abscesses (Fig. 56a) (see also pp. 86-87).
Subcapsular haematomas present as an echo-free or complex (due to
blood clots) area located between the capsule of the liver and the
underlying liver parenchyma. The outline of the liver is not usually
altered (Fig. 56b).
Extracapsular haematomas present as an echo-free or complex (due to
blood clots) area adjacent to the liver but lying outside the capsule. The
ultrasound appearance may be similar to that of an extrahepatic
abscess.
Any patient with an injury to the liver may have several haematomas.
located within the parenchyma. below the capsule or outside the liver.
Other organs. particularly the spleen and kidneys. should also be
examined.
Bi/omas
Liver 89
Fig. 56a. An intrahepatic
haematoma.
Fig. 56b. Two scans of a
large subcapsular haematoma
of the liver.
Fluid within or around the liver may be bile. resulting from trauma to the
biliary tract. It is not possible to distinguish biloma from haematoma by
ultrasound imaging.
90
Notes
CHAPTER 9
Gallbladder and biliary tract
Indications 93
Preparation 93
Normal anatomy of the gallbladder 94
Nonvisualization of the gallbladder 97
Enlarged (distended) gallbladder 98
Echoes within the gallbladder 100
Thick gallbladder walls 104
Small gallbladder 106
Jaundice 107
Clonorchiasis 110
Gallbladder and biliary tract 93
Indications
1. Pain in the right upper abdomen: suspected gallstones and/or
cholecystitis.
2. Jaundice.
3. Palpable right upper abdominal mass.
4. Recurrent symptoms of peptic ulcer.
5. Pyrexia of unknown origin.
Preparation
only water should be given. If the symptoms are acute, proceed with
the examination. Infants-clinical condition permitting-should be
given nothing by mouth for 3 hours preceding the examination.
2. Position of the patient. Start with the
patient lying supine: the patient may later (
need to be turned on to the left side or
examined erect or on hands and knees.
Apply coupling agent liberally to the right
upper abdomen. Later cover the left upper
abdomen also, because, whatever the
symptoms, both sides ofthe upper abdomen
should be scanned.
Perform the scans with the patient holding
the breath in or with the abdomen "pushed
out" in full expiration.
3. Choice of transducer. For adults, use a
3.5 MHz transducer. Use a 5 MHz trans-
ducer for children and thin adults.
abdomen (the xiphOid angle). Angle the beam
to the right side of the patient to image the
liver; adjust the gain to obtain the best
image (see p. 50).
Scanning technique
y
patient breathes in
Start with longitudinal scans, then transverse scans; add intercostal
scans if needed. Then turn the patient on to the left side and make
oblique scans at different angles.
~ -
. .>-
-t .... - .
<; ......
00
""
V
V V
If there is excessive gas in the bowel, examine the patient standing erect
(sitting up will not usually displace bowel gas).
The hands/knees position can be used to demonstrate gallstones more
clearly, allowing the stones to move anteriorly.
V ?
-
3.5 MHz 5 MHz
adults children
~ .. \
angle
transducer
94 Gallbladder and biliary tract
Normal anatomy of the gallbladder
On the longitudinal scan the gallbladder will appear as an echo-free,
pear-shaped structure. It is very variable in position, size and shape, but
the normal gallbladder is seldom more than 4 cm wide (Fig. 57).
Fig. 57a. Longitudinal scan: normal full gallbladder.
Fig. 57b. Longitudinal scan: normal, partially empty gallbladder.
The gallbladder may be mobile. It may be elongated and on scanning
may be found below the level of the superior iliac crest (especially when
the patient is erect). It may be to the left of the midline. If not located in
the normal position, scan the whole abdomen, starting on the right side.
)4
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The thickness of the gallbladder wall can be measured on transverse
scans; in a fasting patient it is normally 3 mm or less and 1 mm when
the gallbladder is distended (Fig. 58) (see p. 104).
Fig. 58a. Transverse scan: normal , full gallbladder (wall thickness 1 mm).
Fig 58b. Longitudinal (upper) and transverse (lower) scans of a contracted gallbladder (wall
thickness less than 3 mm).
If the gallbladder is not identified in its usual position,
scan the whole abdomen and the pelvis. If necessary,
rescan after 6-8 hours, or ask a colleague to scan the
patient.
Failure to demonstrate the gallbladder with ultrasound
does not mean it is absent.
It is not always easy to identifY the normal main right and left hepatic
biliary ducts, but when Visible they are within the liver and appear as
thin-walled tubular structures. However, the common hepatic duct can
usually be recognized just anterior and lateral to the crossing portal
vein, and its cross-section at this level should not exceed 5 mm. The
diameter of the common bile duct is variable but should not exceed 9 mm
near its entrance into the pancreas (Fig. 59) (see also p. 108).
Scanning a jaundiced patient is discussed in detail on pp. 107-109.
Fig. 59a. Oblique scan: normal common bile duct.
Fig. 59b. Transverse scan: the common bile duct at the porta hepatis.
Fig. 59c. Oblique scan: the common bile duct at the porta hepatis.
Nonvisualization of the gallbladder
There are various reasons why the gallbladder may not be seen by
ultrasound:
1. The patient has not been fasting: re-examine after an interval of at
least 6 hours without food or drink.
2. The gallbladder lies in an unusual position.
Scan low down in the right abdomen. even as far as the pelvis.
Scan to the left of the midline and with the patient in the oblique
position with the right side down.
Scan high under the costal margin.
v
v
3. The gallbladder is congenitally hypoplastic or absent.
4. The gallbladder is shrunken and full of stones (calculi). with
associated acoustic shadowing.
5. The gallbladder has been removed surgically: examine the abdomen
for scars and ask the patient (or relatives).
6. The examiner is not properly trained or experienced: ask a colleague
to examine the patient.
There are very few pathological conditions (other than congenital
absence or surgical removal) that result in persistent nonvisualization
of the gallbladder by ultrasound.
~
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i
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'v'
congenital shrunken.
absence with calculi
no food for
at least 6 hours
v
~ t ~
surgical
removal
Enlarged (distended) gallbladder
The gallbladder is enlarged if it exceeds 4 cm in width (transverse
diameter).
The normal gallbladder may appear distended when the patient is de-
hydrated, has been on a low-fat diet or on intravenous nutrition, or has
been immobilized for some time. If there is no clinical evidence of
cholecystitis, and if the gallbladder wall does not appear thickened on
ultrasound, give the patient a fatty meal and repeat the ultrasound
examination in 45 minutes to 1 hour. A normal gallbladder will contract
(Fig.60a).
If there is no contraction, search for:
1. A gallstone or other cause of obstruction within the cystic duct. The
hepatic and bile ducts will be normal. If there is no internal
obstruction, there may be a mass or lymph node pressing externally
on the duct.
2. A stone or other obstruction in the common bile duct. The common
hepatic duct will be dilated (over 5 mm diameter). Examine the
common bile duct for Ascaris (Fig. 60b): ona transverse scan, a tube
within a tube is the "target" sign (Fig. 60c). Look for Ascaris also in
the stomach or small bowel. Obstruction may be due to a carcinoma
at the head of the pancreas (a hypoechogenic mass), or where
hydatid disease is endemic. cyst membranes in the common
duct. (Scan the liver and the abdomen for cysts. and X-ray the
chest.)
Fig. 60a. Left: the gallbladder is full. Right: the gallbladder has contracted after a
fatty meal.
Fig. 60b. Longitudinal scan: Ascaris in the common bil e duct.
Fig. 60c. Transverse scan: Ascaris in the common bile duct: this shows the "target" sign.
3. If the gallbladder is distended with thickened walls (greater than
5 mm) and filled with fluid. there may be an empyema: local
tenderness is likely. Check the patient clinically (Fig. 61).
4. If the gallbladder is distended with thin walls and filled with fluid.
there may be a mucocele. This does not usually result in local
tenderness.
Fig. 61a. Transverse scan: a distended gallbladder with thick walls.
Fig. 61 b. Longitudinal scan: the same distended. thick-walled gallbladder.
Acute cholecystitis
Clinically. acute cholecystitis is usually associated with pain in the right
upper abdomen and with local tenderness when the transducer is
(carefully) applied near the gallbladder. There may be one or more
gallstones. probably including a stone in the gallbladder neck or in the
cystic duct (see pp. 100-102). The walls of the gallbladder are likely to
be thickened and oedematous. and. therefore. the gallbladder is not
always distended. If the gallbladder has perforated. there is usually fluid
adjacent to it.
/
I
\

Gallstones do not always cause symptoms: exclude
other disease even when there are gallstones.
Echoes within the gallbladder
Mobile internal echoes with shadowing
1. Gallstones can be recognized as bright intraluminal echogenic
structures with an acoustic shadow. The stones may be single or
multiple, large or small, calcified or non-calcified. The gallbladder
walls may be normal or thickened (Fig. 62a, b).
Fig. 62a. Transverse scan: a single stone in the gallbladder.
Fig. 62b. Longitudinal scans: multiple small gallstones (left) ; two large gallstones (right).
2. When gallstones are suspected but not seen clearly on routine
scans, rescan with the patient oblique or erect. Most gallstones will
change position within the gallbladder as the patient moves
(Fig 62c, d) (see also p. 101).
Fig. 62c. A gallbladder containing a large solitary stone.
Fig. 62d. When the same patient is moved, the gallstone changes position.
Gallbladder and biliary tract -101
3. If there is still any doubt, scan the patient in the hands/knees
position. The gallstones will move anteriorly. This position may also
be useful if there is excessive bowel gas (Fig. 62e, 0.
Fig. 62e. An unsuccessful scan, because the gallbladder is obscured by gas in the bowel.
Fig. 62f. With the same patient in the hands/knees position, the gallbladder is seen clearly.
Ultrasound can reliably diagnose gallstones when they
are in the gallbladder.
Ultrasound is not always reliable in recognizing stones
in the bile ducts.
Gallstones do not always cause symptoms: exclude
other disease even when there are gallstones.
Mobile internal echoes without shadowing
Scans should be taken in different positions. The common causes are:
1. Gallstones. Note that there will be no acoustic shadow if the stones
are smaller than the diameter of the ultrasound beam (Fig. 63a).
2. Gallbladder sludge. This is thickened bile which produces fine
dependent echoes that move slowly with a change in the position of
the patient. unlike stones which tend to move quickly (Fig. 63b).
3. Pyogenic debris (Fig. 63c).
4. Blood clots.
5. Hydatid membranes. Scan the liver for cysts (see pp. 81-83).
6. Ascaris and other parasites. It is unusual for worms such as Ascaris
to reach the gallbladder. They are more likely to be seen in the bile
duct (see p. 98). In clonorchiasis the hepatic ducts will be dilated
and irregular and there is often much intraductal debris
(see p. 110).
Fig. 63a. Transverse scan: the gallbladder is very distended and contains fine sludge. The
distension was due to a small stone in the cystic duct, which did not produce an acoustic
shadow.
Fig. 63b. Longitudinal scan: sludge in the gallbladder: the thickened walls are the result of
chronic inflammation.
Fig. 63c. Thick sludge and debris in the gallbladder from pyogenic infection.
Nonmobile internal echoes with shadowing
The commonest cause is an impacted calculus (Fig. 64a): search for
other calculi. The calcification may also be in the gallbladder wall: if the
wall is also thickened. there may be acute or chronic cholecystitis. but
it may be difficult to exclude an associated carcinoma (see p. 105).
Nonmobile internal echoes without shadowing
1. The most common cause is a polyp (Fig. 64b). It may be possible to
identity the pedicle by using different scanning projections. There
should be no acoustic shadowing. and changing the patient's
position will not move the polyp but may alter its shape. Malignant
disease may resemble a polyp but is more often associated with
thickening of the gallbladder wall and does not usually have a
pedicle. A malignant tumour is less likely to change its shape when
the patient changes position (see p. 105).
2. A septum or fold within the gallbladder is not likely to be of any
clinical significance (see p. 105).
3. A malignant tumour (Fig. 64c) (see p. 105).
Fig. 64a. Transverse scan of the gallbladder: there will probably be distension when there is a
stone impacted in the neck of the gallbladder.
Fig. 64b. Longitudinal scan of the gallbladder showing a small pedunculated polyp.
Figure 64c. Longitudinal scan: a small sessile tumour in the gallbladder.
Thick gallbladder walls
Generalized thickening
The thickness of the gallbladder wall is nonnally less than 3 mm and
should not exceed 5 mm. When the thickness is between 3 mm and
5 mm, careful clinical correlation is needed. Generalized thickening of
the gallbladder wall can occur in the following conditions:
1. Acute cholecystitis. This may be associated with an echo-free
section in the wall or a localized fluid collection. Stones may be
present: check the neck of the gallbladder (see p. 99).
2. Chronic cholecystitis (Fig. 65a). There may also be stones (see
pp. 100-102).
3. Hypoalbuminaemia resulting from cirrhosis. Check for ascites,
dilated portal veins and splenomegaly.
4. Congestive cardiac failure (Fig. 65b). Check for ascites, pleural
effUSions, and dilated inferior vena cava and hepatic veins (see
pp. 68 and 76). Examine the patient.
5. Chronic renal insufficiency. Examine the kidneys and the urine.
6. Multiple myeloma. Laboratory tests are necessary.
7. Hyperplastic cholecystosis. This is usually asymptomatic. Aschoff-
Rokitansky sinuses are best seen on oral cholecystography,
occasionally with ultrasound.
8. Acute hepatitis.
9. Lymphoma.
Fig. 65a. A gallbladder with thick walls due to chronic cholecystitis: the bile is thickened,
forming sludge.
Fig. 65b. A small gallbladder with thick walls in a patient with cardiac failure.
normal
<3mm
correlate
-clinically
3-5mm
_abnormal
>5mm
Localized thickening
Local thickening of the gallbladder walls may be due to the following:
1. Mucosal folds. There may be several together. Scan in different
positions: pathological thickening (more than 5 mm in any area) will
not alter with the position of the patient, but folds will vary in
thickness and position (Fig. 65c).
2. Polyp. There will be no movement with a change in the patient's
position (Fig. 65d), but the shape may alter.
3. Primary or secondary carcinoma ofthe gallbladder. This appears as
a thick, irregular, solid intramural mass, localized and not changing
with the patient's position (Fig. 65e).
Fig. 65c. A mucosal fold in the gallbladder. Rescanning in different positions, or after an
interval, is essential to establish the correct diagnosis.
Fig. 65d. A small pedunculated polyp. This will not move but may alter its shape when the
patient is scanned in a different position.
Fig. 65e. Carcinoma of the gallbladder.
Small gallbladder
1. The patient may recently have had a meal
containing fat and the gallbladder has
contracted.
2. Chronic cholecystitis: check for thickened
gallbladder walls and for gallstones within
the gallbladder (Fig. 66a) (see pp. 100-102).
Fig. 66a. A small thick-walled gallbladder containing several stones.
If the gallbladder is small, re-examine after 6-8 hours
(without food or drink) to differentiate between an
empty gallbladder and a contracted gallbladder. The
normal gallbladder will fill up after a few hours and
appear normal in size.
Fig. 66b. A normal gallbladder is small when empty (left) and will be much larger when full
(right).
The patient has
had a meal
with fat
Jaundice
When the patient is jaundiced, ultrasound can usually differentiate
between non-obstructive and obstructive jaundice, by showing the
dilatation of the biliary system. However, the exact cause ojthejaundice
may be difficult to identify. .
ULTRASOUND IN JAUNDICE
Normal bile ducts
Normal
liver
parenchyma
Abnormal
liver
parenchyma
Diffuse
liver
disease
Nodular
mass
Single
mass
Multiple
masses
Biopsy with thin needle
Dilated bile ducts
Dilated
intrahepatic
ducts
I
I I
Dilated
extrahepatic
ducts
I
Dilated at level of:
common hepatic duct
common bile duct
pancreatic duct
Percutaneous
cholangiography
Retrograde
pancreatog raphy
When the patient is jaundiced, ultrasound can provide information
about the gallbladder and the biliary ducts, and can usually
differentiate between obstructive and non-obstructive jaundice, but
does not always show the exact cause.
I
I In every jaundiced patient, scan the liver, the biliary tract and both
sides of the upper abdomen.
Technique
The patient should be supine, with the right side slightly
elevated. Ask the patient to take a deep breath and hold it
in while the scan is being perfonned.
For an adult, use a 3.5 MHz transducer. For a child or thin
adult, use a 5 MHz transducer.
Start with sagittal or slightly oblique scans; identify the inferior vena
cava and the main portal vein lying anteriorly. This will make it easier
to locate the common hepatic duct and the common bile duct, which
should be seen angling from the liver anteriorly to the portal vein and
descending to the pancreas (Fig. 59) (see p. 96).
In one-third of patients, the bile duct will be more lateral to the portal
vein and is better seen by oblique longitudinal scanning (Fig. 67a).
Normal bile ducts
1. Extrahepatic ducts. lt may be difficult to see the extrahepatic bile
ducts, particularly with a linear transducer. Use a curvilinear or
sector transducer if available. Move the patient into different
pOSitions, varying the scanning technique as much as possible
whenever the extrahepatic duct needs to be demonstrated (Fig.
67a).
2. Intrahepatic ducts. The intrahepatic ducts are best seen on the left
side of the liver in deep inspiration (Fig. 67b). It is not easy to see the
nonnal intrahepatic ducts on ultrasound because they are often too
small and thin-walled. However, whentheductsaredUated, they are
easUy seen and show as numerous, branching irregular structures
throughout the liver substance (the "branching tree" effect) near the
portal veins (Fig. 67b).
Fig. 67a. Dilated extrahepatic bile ducts.
Fig. 67b. Dilated intrahepatic bile ducts.
y
3.5 MHz
adults
5MHz
children
Gal/bladder in jaundice
1. If the gallbladder is distended, the obstruction usually
affects the common bile duct (e.g. calculus, Ascaris,
acute pancreatitis or carcinoma). The hepatic ducts will
also be distended (Fig. 68a).
2. If the gallbladder is not distended or is very small
Fig. 68b), obstruction is unlikely or the obstruction is
above the level of the cystic duct (e.g. enlarged lymph
nodes or tumour near the porta hepatis).
Biliary tract in jaundice
Maximum diameter of normal common
hepatic duct: less than 5 mm
Maximum diameter of normal common
bile duct: less than 9 mm
Maximum diameter of common bile
duct post-cholecystectomy: 10-12 mm
Sometimes following surgery, and in patients over 70 years
of age, the common bile duct may be a few millimetres wider
(I.e. 12-14 mm) (Fig. 68c). Add 1 mm to all of the
measurements above for each decade over 70 years of age.
1. If the intrahepatic ducts are mildly dilated, suspect
biliary obstruction which can be recognized on
ultrasound before there is clinical jaundice (Fig. 68d).
If in the early stages of jaundice the bile ducts are not
dilated, rescan after 24 hours.
2. If the extrahepatic ducts are dilated, but not the intra-
hepatic ducts, scan the liver parenchyma. If jaundice is
persistent, the cause may be cirrhosis. But also exclude
obstruction of the lower common bile duct
(Fig. 68e).
Dilated intrahepatic ducts are best seen by scanning the
sub-xiphoid region to show the left lobe of the liver. They will
appear as tubular structures parallel to the portal vein, both
centrally and extending into the periphery of the liver.
If it seems that there are two vessels running parallel, one
is most likely a dilated bile duct, which will also be seen
extending elsewhere in the liver, probably about the same
size as the portal veins.
Fig. 68a. A distended gallbladder.
Fig. 68b. A small gallbladder with
distended bile ducts (due to an enlarged
lymph node at the porta hepatis).
Fig. 68c. Mildly dilated bile ducts.
Fig. 68d. Dilated common bile duct
containing a gallstone.
Clonorchiasis
In clonorchiasis. the common and hepatic bile ducts are dilated.
irregular and saccular. whereas in obstructive jaundice without
cholangitis. the ducts are smoothly dilated and seldom saccular. It is
possible to recognize intraductal debris in clonorchiasis but the actual
parasites are too small to be imaged with ultrasound (Fig. 69).
Ifboth the hepatic and extrahepatic bile ducts are dilated and there are
large cystic lesions within the liver parenchyma. there is probably
hydatid disease. not clonorchiasis (see pp. 82-83).
Fig. 69a. Longitudinal scan: dilated and irregular bile ducts due to infective cholangitis. often
associated with clonorchiasis.
Fig. 69b. Transverse scan: dilated. saccular bile ducts filled with debris from infection. Gross
distension such as this is found in clonorchiasis.
Ultrasound can diagnose gallstones in the gallbladder
but is not always reliable in recognizing stones in the
common bile duct. Clinical judgement must be used,
especially in the jaundiced patient.
CHAPTER 10
Pancreas
Indications 112
Preparation 112
Normal pancreas 117
Small pancreas 118
Diffuse enlargement of the pancreas 119
Focal enlargement (noncystic) 119
Pancreatic cysts 120
Calcification in the pancreas 121
Dilatation of the pancreatic duct 122
Common errors 123
112 Pancreas
Indications
1. Midline upper abdominal pain, acute or chronic.
2. Jaundice.
3. Upper abdominal mass.
4. Persistent fever, especially with upper abdominal tenderness.
5. Suspected malignant disease.
6. Recurrent chronic pancreatitis.
7. Suspected complications of acute pancreatitis, especially pseudocyst
or abscess.
8. Polycystic kidneys: cysts in the liver or spleen.
9. Direct abdominal trauma, particularly in children.
If there is acute abdominal pain, an erect radiograph of the upper
abdomen, including both sides of the diaphragm, is needed to exclude
perforation of a hollow viscus.
Preparation
prevent dehydration, only water should be given. If the symptoms
are acute, proceed with the examination. Infants-clinical condition
the examination.
2. Position ofthe patient. The patient should
be supine but may need to be examined in
the oblique or both decubitus positions: if
necessary, a scan can be done with the
patient sitting partially upright or in the
erect position.
oblique decubitus
Apply coupling agent liberally across the
upper abdomen on both sides.
y
obtain the best image (see p. 50).
Scanning technique
~ . 5 MHz
~ adults
patient breathes in
Pancreas 113
?
5 MHz
children
The pancreas can be very difficult to identify, especially the tail.
Start with transverse upper abdominal scans
moving from side to side and from the costal
margin towards the umbilicus. Then perform
longitudinal scans moving up and down across
the upper abdomen. When it is necessary to
examine a specific area, ask the patient to take
a deep breath and hold it in.
Gas
If bowel gas obscures the image:
1. Try gentle compression with the transducer
or use decubitus views, both right and left.
~ ...
" .. >-
" ......... >-
-( ....... >-
""
v
2. If necessary, give the patient 3 or 4 glasses
of water, wait a few minutes to allow the
bubbles to disperse and then repeat the
examination with the patient siUing or
standing, viewing the pancreas through the
water-filled stomach.
~ ~

"', ....
1 2
~
3. If the patient cannot stand, let him or her lie
on the left side and drink through a straw.
Then scan with the patient supine (see
also p. 116).
then scan
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114 Pancreas
Transverse scanning
Start with transverse scans across the abdomen moving downwards
towards the feet until the splenic vein is seen as a linear, tubular
structure with the medial end broadened. This is where it is joined by
the superior mesenteric vein, at the level of the body of the pancreas. The
superior mesenteric artery will be seen in cross-section just below the
vein. By angling and rocking the transducer, the head and the tail of the
pancreas may be seen (Fig. 70).
Continue transverse scans downwards to visualize the head of the
pancreas and the uncinate process (if present) between the inferior vena
cava and the portal vein (Fig. 70a).
Fig. 70a. Transverse scan: the splenic vein, superior mesenteric artery and the body of the
pancreas.
Fig. 70b. Transverse scan: the head of a normal pancreas scanned through the left lobe of the
liver.
Fig. 70c. Transverse scan: the tail of a normal pancreas.
...
-<
-<
-<
-c-
v
Fig. 70d. Transverse scan: the normal pancreatic duct.
Longitudinal scanning
Start longitudinal scanning just to the right of the midline and identify
the tubular pattern of the inferior vena cava with the head of the
pancreas anteriorly. below the liver. The vena cava should not be
compressed or flattened by a normal pancreas (Fig. 7la).
Continue longitudinal scans moving to the left. Identify the aorta and the
superior mesenteric artery. This will assist in identifying the body of the
pancreas (Fig. 7lb).
Fig. 71 a. Longitudinal scan: the inferior vena cava and the head of the pancreas.
Fig. 71 b. Longitudinal scan: the body of the pancreas.
Pancreas 115
v
116 Pancreas
Decubitus scanning
Mter the transverse and longitudinal scans. turn the patient onto the
right side and scan the pancreas through the spleen and the left kidney.
This will demonstrate the tail of the pancreas.
Then. with the patient lying on the left side. ask him/her to take a deep
breath and hold it in. Scan the pancreas through the liver. This will show
the head of the pancreas (Fig. 72).
Fig. 72a. The head of the pancreas is obscured by bowel gas when the patient is supine.
Fig. 72b. When the same patient is in the left decubitus position. the bowel gas has moved and
the pancreas is seen clearly.
Erect scanning
When visualization is poor because of bowel gas. let the patient drink
3 or 4 glasses of water. Once the patient has finished drinking wait a
few minutes for the bubbles to disperse. Then. with the patient sitting
or erect, scan the pancreas through the stomach. This technique is
particularly useful for visualizing the tail of the pancreas (Fig. 72c, d)
(see also p. 113).
After patient has finished
drinking. wait a few
minutes before scanning
full inspiration
Fig. 72c. Immediately after the patient drinks water, wait before scanning. Microbubbles in the
stomach may obscure the pancreas.
Fig. 72d. With the patient erect, the pancreas can be scanned through the stomach.
Imaging the entire pancreas is often difficult. Different
positions and scanning angles must be used.
Normal pancreas
The pancreas has about the same echogenicity as the adjacent liver and
should appear homogeneous. However, the pancreatic echogenicity
increases with age. The outline of the normal pancreas is smooth.
When scanning the pancreas, certain anatomical landmarks should be
identified, in the following order:
1. Aorta
2. Inferior vena cava
3. Superior mesenteric artery
4. Splenic vein
5. Superior mesenteric vein
6. Wall of the stomach
7. Common bile duct
The essential landmarks are the superior mesenteric artery and the
splenic vein.
Pancreas 117
118 Pancreas
Normal pancreatic size
There is great variability in the size and shape of
the pancreas. The following gUidelines may be
helpful.
1. The average diameter of the head of the
pancreas (A): 2.8 cm.
2. The average diameter of the medial part of
the body of the pancreas (B): less than
2 cm.
3. The average diameter of the tail of the
pancreas (C): 2.5 cm.
Fat patient
Thin patient
B
4. The diameter of the pancreatic duct should
not exceed 2 mm. It is normally smooth. and
the wall and the lumen can be identified.
The accessory pancreatic duct is seldom
visualized.
A
0- sup. meso
t e ~
Small pancreas
p aorta
info vena cava 0
spine
The pancreas is usually smaller in elderly people. but this is not of
clinical significance. When there is overall atrophy of the pancreas. the
decrease in size is usually uniform throughout the pancreas. If there
appears to be atrophy of the tail of the pancreas alone (the head
appearing normal). then a tumour in the head of the pancreas must be
suspected (Fig. 73a). The head must be scanned carefully because
chronic pancreatitis in the body and tail may be associated with a slow-
growing tumour in the head of the pancreas.
Fig. 73a. Atrophy of the tail of the pancreas.
If the pancreas is small and irregularly hyperechogenic and non-
homogeneous compared with the liver. the cause is usually chronic
pancreatitis (Fig. 73b).
Fig. 73b. A small. nonhomogeneous pancreas with calcifications due to chronic pancreatitis.
Diffuse enlargement of the pancreas
In acute pancreatitis, the pancreas may be diffusely enlarged and either
normal or hypoechogenic compared with the adjacent liver. The serum
amylase is usually elevated, and there may be local ileus due to bowel
irritation.
When the pancreas is irregularly hyperechogenic and diffusely enlarged,
there is usually acute pancreatitis superimposed on chronic pancreatitis
(Fig. 74a).
Fig. 74a. Transverse scan: acute pancreatitis.
Focal enlargement (noncystic)
Almost all pancreatic tumours are hypoechogenic compared with the
normal pancreas. It is not possible to distinguish between focal
pancreatitis or pancreatic tumour by ultrasound alone. Even if the
serum amylase is elevated, repeat the ultrasound examination in
2 weeks to assess the change. Tumour and pancreatitis can co-exist.
When the pattern is mixed, biopsy is needed (Fig. 74b).
Fig. 74b. Longitudinal scan: focal, noncystic enlargement of the pancreas due to chronic
pancreatitis. A tumour could have the same appearance.
Echogenicity
relative to the
adjacent liver
Tumour
Low
Acute
pancreatitis,
diffuse or
local
Low
Chronic
pancreatitis
High
Aging
normal
pancreas
High
Pancreas 119
120 Pancreas
Pancreatic cysts
True pancreatic cysts are rare. They are usually single. echo-free.
smooth cavities filled with fluid. Small multiple cysts may be con-
genital. An abscess or haematoma in the pancreas will appear as a
complex mass. often associated with severe pancreatitis.
Pseudocysts following trauma or acute pancreatitis are not uncommon;
they may increase in size and rupture. Such cysts can be single or
multiple. In the early stages they are complex. with internal echoes and
ill-defined walls. but eventually these cysts become smooth-walled and
echo-free. with good sound transmission (Fig. 75a). Pancreatic
pseudocysts may be found anywhere in the abdomen or pelvis. often
remote from the pancreas. When the cysts are infected or damaged.
there may be internal echoes or septation.
Pancreatic cystadenoma or other cystic tumours usually appear on
ultrasound as multiseptate cystic masses with associated solid
components (Fig. 75b). In microcysticadenomata the cysts are very
small and difficult to image.
Hydatid cysts (Fig. 75c) are unusual in the pancreas. Scan the liver and
the rest of the abdomen to exclude hydatid disease (see pp. 82-83).
Fig. 75a. Longitudinal scan: a pseudocyst of the pancreas.
Fig. 75b. Longitudinal scans: cystadenocarcinoma of the pancreas.
Fig. 75c. Transverse scan: hydatid cyst of the pancreas.
Calcification in the pancreas
Ultrasound is not the best way to assess pancreatic calcification. A
supine antero-posterior radiograph of the upper abdomen is preferable.
Calcification within the pancreas can produce acoustic shadowing.
However, if the calcification is very small, there may only be bright
discrete echoes without shadowing. Calcification is usually due to:
1. Chronic pancreatitis. Calcification is distributed throughout the
pancreas (Fig. 76a, b).
2. Calculi in the pancreatic duct. This calcification follows the
anatomical pattern of the duct (Fig. 76c).
3. Biliary calculi in the distal common bile duct can be mistaken for
pancreatic calcification. There is usually dilatation of the proximal
bile duct.
Fig. 76a. Chronic pancreatitis with calcification.
Fig. 76b. Transverse (left) and longitudinal (right) scans of chronic pancreatitis with
calcification.
Fig. 76c. Transverse scan: a large calculus in the pancreatic duct.
Pancreas 121
122 Pancreas
Dilatation of the pancreatic duct
The nonnal maximum internal diameter of the pancreatic duct is 2 mm,
and it is best identified on a transverse scan of the mid portion of the
body of the pancreas. To ensure proper identification of the duct,
pancreatic tissue should be recognized on either side of it. If not, either
the splenic vein posteriorly or the wall of the stomach anteriorly may
cause confusion (Fig. 77a).
Fig. 77a. The internal diameter of a normal pancreatic duct should be less than 2 mm.
The walls of the pancreatic duct should be smooth and the lumen clear.
When the duct is dilated, the walls become irregular; scan not only the
head of the pancreas but also the biliary tract (Fig. 77b).
The causes of dilatation of the pancreatic duct are:
1. Tumour of the head of the pancreas or ofthe ampulla of Vater. Both
are usually associated with jaundice and dilatation of the biliary
tract.
2. Calculus in the common pancreatic duct. Scan to visualize biliary
calculi and bile duct dilatation (see pp. 96 and 107-109).
3. Calculus in the intrapancreatic duct. The biliary tract should be
nonnal.
4. Chronic pancreatitis (see pp. 118-119 and 121).
5. Postoperative strictures following Whipple's operation or partial
pancreatectomy. The clinical history should be verified with the
patient or relatives if necessary.
Fig. 77b. Transverse scan: a markedly dilated pancreatic duct.
Pancreas 123
'24
Notes
CHAPTER 11
Spleen
Indications 126
Preparation 126
Normal spleen 128
Abnormal spleen 129
Trauma 134
------ -
126 Spleen
Indications
1. Splenomegaly (enlarged spleen)
2. Left abdominal mass
3. Blunt abdominal trauma
4. Left upper abdominal pain (an erect abdominal X-ray, including
both sides of the diaphragm, is also needed if perforation of the
bowel is suspected)
5. Suspected subphrenic abscess (pyrexia of unknown origin)
6. Jaundice combined with anaemia
7. Echinococcosis (hydatid disease)
8. Ascites or localized intra-abdominal fluid
9. Suspected malignancy, especially lymphoma or leukaemia
Preparation
prevent dehydration, only water should be given. If the symptoms
are acute, proceed with the examination. Infants-clinical condition
the examination.
For acutely ill patients (e.g. trauma, sudden abdominal pain, post-
surgical pyrexia), no preparation is needed.
be supine initially and later on the right side.
Apply coupling agent liberally over the left
lower chest, the upper abdomen and left
flank.
The patient should take a deep breath and
hold it in when a specific area is being
scanned.
y
~ \ ~
3. Choice oftransducer. For adults, use a 3.5 MHz sector transducer.
For children and thin adults, use a 5 MHz sector transducer. A small
sector transducer is helpful. if available.
3.5 MHz
adults
5MHz
children
4. Setting the correct gain. Start by placing the transducer centrally
at the top of the abdomen (the xiphoid angle). Angle the beam to the
right side of the patient to image the liver; adjust the gain to obtain
the best image (see p. 50).
~ .. \
angle
transducer
patient breathes in patient holds breath in
Scanning technique
Scan with the patient in the supine and oblique positions. Multiple
scans may be necessary.
..,",
30,? / .
/'
/' .
~ . -_. -_ ... -_ ... -_ ... -_ ... - .... -----:.
supine
oblique 30
Scan from below the costal margin, angling the beam towards the
diaphragm, then in the ninth intercostal space downwards. Repeat
through all lower intercostal spaces, first with the patient supine and
then with the patient lying obliquely (30) on the right side.
----=---------------
.. ~ .
J;:
:-.. ~
. ~ . ~ ~
Also perform longitudinal scans from anterior to posterior axillary lines
and transverse upper abdominal scans. Scan the liver also, particularly
when the spleen is enlarged .
.
-<:- .>-
-<:E ........ >-
--(- ..... >-
Spleen -127
128 Spleen
Normal spleen
It is important to identify the:
1. Left hemi-diaphragm.
2. Splenic hilus.
3. Splenic veins and relationship to pancreas.
4. Left kidney (and renal/splenic relationship).
5. Left edge of liver.
6. Pancreas.
When the spleen is normal in size, it can be difficult to image completely.
The splenic hilus is the reference point to ensure correct identification
of the spleen. Identify the hilus as the enby point for the splenic vessels
(Fig. 78).
It is important to identify the left diaphragm and
the upper edge of the spleen.
Fig. 78. Oblique scan: normal spleen and left kidney.
Echo pattern
The spleen should show a uniform homogeneous echo pattern. It is
slightly less echogenic than the liver.
High
Renal
alnus
Liver
Echogenicity
Spleen
Renal
cortex
Renal
medulla
,: ... ... .' - -....... ,:" . ",' -. -, ' ." ,
spleen.
_ -. .. -' -;. ' u_ .
splenic
lesion. i ,-
: .--.. '-' :<l1li
. the pancreas .
. ,;, ." - ;'"
.
. . t,,,
II -- --..:::... ;". ,'A
beforelooking'at the spleen.
.> ..... ... ;, . ... . . ,
Low
Abnormal spleen
Enlarged spleen/splenomegaly
There are no absolute criteria for the
size of the spleen on ultrasound. When
normal, it is a little larger than or about
the same size as the left kidney. The
length should not exceed 15 cm in the
major axis.
A chronically enlarged spleen may often
distort and displace the left kidney,
narrowing it in both the antero-posterior
diameter and the width.
Homogeneous splenomegaly
This may be due to:
/
v
\ .
. "" less than
15 em
1. Tropical splenomegaly, which includes idiopathic splenomegaly,
malaria, trypanosomiasis, leishmaniasis and schistosomiasis
(Fig. 79a).
2. Sickle cell disease (unless infarcted).
3. Portal hypertension.
4. Leukaemia (Fig. 79b).
4. Metabolic disease.
5. Lymphoma (may contain hyperechogenic masses).
6. Infections such as rubella and mononucleosis.
Whenever there is splenomegaly, examine the liver for size and
echogenicity. Also examine the splenic and portal veins, the inferior
vena cava, hepatic veins and mesentery for thickening. The region near
the hilum ofthe spleen should be scanned for tubular structures due to
varicosities.
spine
Fig. 79a. Longitudinal scan: gross splenomegaly (due to leishmaniasis) compressing the left kidney.
Fig. 79b. Transverse scan: hepatosplenomegaly due to leukaemia.
Spleen -129
.--
- \
130 Spleen
Non-homogeneous spleen, with or without splenomegaly
Well defined cystic lesion
If there is a clearly demarcated, echo-free mass with posterior acoustic
enhancement, differentiate:
1. Cystic disease (may be multiple). Examine liver and pancreas for
cysts.
2. Congenital cysts. These are usually solitary and may contain
echoes as a result of haemorrhage (Fig. 80a).
Fig.80a. Longitudinal scans: a septate cyst in the spleen, found incidentally.
3. Echinococcal (hydatid) cysts. These are usually clearly defmed
with a double wall (the pericyst and the cyst wall) and often septate.
There will be markedly enhanced back wall echoes and often
marked variation in the thickness of the wall of the cyst. However.
hydatid cysts may appear as roughly rounded masses with an
irregular contour and a mixed echo pattern resembling an abscess.
The cyst can be hypoechogenic with few irregular echoes or
hyperechogenic and solid without any back wall shadow:
combinations of these findings may occur. The walls of the cyst may
be collapsed or sagging and there may be a floating density within
the cyst, or even a cyst within a cyst (which is pathognomonic for
hydatid disease). There may be calcification within the wall of the
cyst and there may be "sand" in the most dependent portion.
Examine the whole abdomen and X-ray the chest. Hydatid cysts are
often multiple but the pattern is variable and cysts in the liver do not
always resemble those in the spleen (Fig. 80b) (see pp. 82-83
and 135).
Fig.80b. Hydatid cysts in the spleen.
4. Haematoma. See p. 134.
If the spleen is enlarged, and there is a history of
trauma, scan the spleen to exclude injury (see p. 134).
A regular but ill-defined cystic lesion in the spleen
Scan in different projections.
1. A hypoechogenic cystic area with an irregular outline, usually
containing debris and associated with splenomegaly and local
tenderness, suggests a splenic abscess (Fig. 8Ia). Examine the liver
for other abscesses (see pp. 78 and 86-87).
After successful treatment, the abscess may resolve or become
larger and almost echo-free, but is no longer tender (Fig. 8Ib).
2. A similar cystic lesion which is larger and contains fluid may be a
splenic abscess following infarction resulting from sickle cell disease.
Amoebic abscesses are very rare in the spleen: bacterial abscesses
are more common.
Splenic vein
A normal splenic vein does not exclude portal hypertension.
Enlarged splenic vein
If the splenic vein appears large and remains more than 10 mm in
diameter on normal respiration, portal hypertension should be suspected.
When the portal vein is more than 13 mm in diameter and does not vary
with respiration, there is a strong correlation with portal hypertension
(Fig. 8Ic).
Spleen -131
Fig. 81a. An early abscess in
the spleen, before treatment.
Fig. 81 b. A splenic abscess
after treatment.
Fig. 81c. Two patients with
dilatation of the splenic vein
and multiple varicosities, the
results of portal hypertension.
-------------
132 Spleen
Intrasplenic mass, with or without splenomegaly
Splenic masses may be single or multiple and well defined or irregular
in outline. Lymphoma is the commonest cause of an intrasplenic mass,
and such masses are usually hypoechogenic (Fig. 82a). Malignant
tumours, either primary or metastatic, are rare and may be either hypo-
or hyperechogenic (Fig. 82b). When there is necrosis there will be a
complex echo pattern, which may suggest an abscess (Fig. 82d, p. 133).
Infections such as tuberculosis or histoplasmosis may cause scattered
granulomas, appearing as hyperechogenic masses, sometimes with
shadowing because of calcification. Haematoma must be excluded (see
pp. 134-135).
Fig. 82a. Two patients with lymphoma of the spleen: a small mass in the spleen on the left, a
much larger mass in the spleen on the right. Both masses are hypoechogenic.
Fig. 82b. Metastasis in the spleen from carcinoma of the ovary.
If there is contraction of the splenic outline near the mass, there may be
an old haematoma or scar from trauma (see pp. 134-135). Alternatively,
there may be an old infarct (e.g. in sickle cell disease) (Fig. 82c).
Fig. 82c. A splenic infarct.
, , '
Whenever there is an intrasplenic mass, exclude recent
injury, particularly when there is splenomegaly.
Splenic abscess: an irregular, hypoechogenic or complex cystic
intrasplenic mass (Fig. 82d). See also pp. 131-132.
Fig. 82d. A large splenic abscess, containing debris and almost filling the spleen.
Pyrexia (usually of unknown origin)
If possible, check the total and the differential white cell count. Start
with longitudinal scans.
A perisplenic, subdiaphragmatic, echo-free or complex mass, superior
to the spleen but limited by the left diaphragm, is probably a subphrenic
abscess. Movement of the diaphragm will usually be reduced. Scan
under the right diaphragm to see if there is fluid on that side. Also scan
the whole abdomen, including the pelvis, to exclude fluid elsewhere.
Scan the left lateral and posterior lower chest for an echo-free area above
the diaphragm indicating pleural fluid, sometimes visible through the
spleen (Fig. 83). A chest X-ray may be helpful.
Fig. 83a. Longitudinal scan: a collection of fluid around the spleen; this was a perisplenic
abscess, but the type of fluid can seldom be identified with an ultrasound scan.
Fig. 83b. A left pleural effusion seen through the spleen.
Spleen -133
134 Spleen
Trauma
The examination should include a sUIVey of the outline of the spleen. to
identifY any area of local enlargement. and then the abdomen to
determine the presence or absence of free intraperitoneal fluid. Repeat
the scan after a few days if the clinical condition of the patient is not
improving.
1. If there is free intraperitoneal or subphrenic fluid and an irregular
splenic outline. a splenic tear or injury is likely (Fig. 84a. b).
2. An echo-free or complex echo area at the periphery of the spleen.
associated with general or localized splenomegaly suggests a
subcapsular haematoma (Fig. 84c). Search carefully for free intra-
abdominal fluid.
3. An intrasplenic echo-free or complex. irregular mass suggests an
acute haematoma (Fig. 84d). An accessory spleen may have the
same appearance (Fig. 84e).
4. An echogenic intrasplenic mass is probably an old haematoma
which has calcified. giving bright echoes with acoustic shadowing.
A haemangioma may have the same appearance (Fig. 84f1.
5. An irregular. echo-free or complex mass may be a traumatic cyst or
a damaged hydatid cyst (Fig. 84g) (see p. 130).
Fig. 84a. A tear in the upper pole of the spleen following injury.
Fig. 84b. Laceration of the spleen with intra-abdominal fluid. probably blood.
Fig. 84c. A left intercostal scan performed eight days after injury. There are subcapsular and
intrasplenic haematomas.
Fig. 84d. An acute haematoma of the spleen without rupture of the splenic capsule.
," _ .. <0-
:
,
(,.-
Accessory spleen
Fig. 84e. An accessory spleen: this could be mistaken for a haematoma or the result of a torn
spleen.
Fig. 84f . An enlarged spleen due to tropical splenomegaly, in which a solitary haemangioma
was an incidental finding. It could be mistaken for an old haematoma or a collapsed cyst.
/ . t . ~ J . . .. ".1\
[ 7/
Hydatid cyst
..... .,: I"
"7"'\-
Splenic vein
Fig. 84g. An old, partially calcified hydatid cyst of the spleen.
Spleen -135
136
Notes
CHAPTER 12
Peritoneal cavity and
gastroi ntesti nal tract
Indications 138
Preparation 138
Normal gastrointestinal tract 140
Intraperitoneal fluid (ascites) 142
Masses in the bowel 143
Suspected appendicitis 147
Gastrointestinal symptoms in children 148
Infection with human immunodeficiency virus 150
138 Peritoneal cavity and gastrointestinal tract
Indications
In adults
1. Suspected ascites and peritonitis
2. Abdominal mass
3. Suspected appendicitis (particularly to exclude other conditions)
4. Localized abdominal pain
In children
1. Localized pain and abdominal masses
2. Suspected hypertrophic pyloric stenosis
3. Suspected intussusception
4. Suspected but indeterminate appendicitis
5. Ascites and peritonitis
Preparation
only water should be given. If the symptoms are acute, proceed with
the examination.
Infants-clinical condition permitting-should be given nothing by
mouth for 3-4 hours preceding the examination. If the child is
vomiting and suspected of having hypertrophic pyloric stenosis, a
warm, sweet, non-aerated drink is necessary to fill the stomach so
that it is possible to check for reflux and observe the passage of fluid
through the pyloric channel (see p. 148).
2. Position of the patient. The patient should be lying on his or her
back (supine) and may be turned obliquely if necessary. It may be
useful to scan the patient erect.
Cover the abdomen
with coupling agent.
oblique
3-4 hours
(except for pyloric
stenosis)
Peritoneal cavity and gastrointestinal tract -139
3. Choice of transducer. For adults, use a 3.5
V3S MHz
MHz transducer. For children and thin adults
adults, use a 5 MHz or 7.5 MHz transducer.

abdomen (the xiphOid angle) . Angle the beam
to the right side of the patient to image the
liver; adjust the gain to obtain the best
image (see p. 50).
patient
breathes in
Scanning technique
Start with longitudinal scans, covering the whole abdomen; then add
transverse and oblique scans, with pressure if necessary to displace the
gas in the bowel.

),.. : : : : : : .
. .. . .. .
.' .... .
:: ::
. ' ., '.
I
I I ,
I
I
.. ".
-r::"::-r

Yyl
If ascites is suspected, see
p. 142.
Correlation with X-rays
may be helpful because
ultrasound cannot ex-
clude perforation of the
bowel. Review antero-
posterior supine and erect
(or decubitus) projections.

-<: ............
oo(
oo( <C\.
oo(
oo(
oo(
-<:
-<E
y

X-ray
g
? 50r75MHz
child ren
! \
angle
transducer
patient holds
breath in
X-ray
[)J
Normal gastrointestinal tract
The different anatomical parts of the gastrointestinal tract can be
recognized.
The oesophagus
The abdominal part of the oesophagus can be visualized with longitudinal
scans, lying inferior to the diaphragm and anterior to the aorta. With
transverse scans, the oesophagus is seen behind the left lobe of the liver
(Fig. 85).
Fig. 85a. Longitudinal scan: the lower oesophagus of a child.
Fig. 85b. Transverse scan: the lower oesophagus of the same child.
The stomach
When empty, the fundus of the stomach will be star-shaped and easily
identified (Fig. 86). The body ofthe stomach will be seen on transverse
scanning, just anterior to the pancreas. If there is confusion, give the
patient one or two glasses of water to distend the stomach.
Fig. 86a. Transverse scan: the fundus of a normal stomach.
Fig. 86b. Transverse scan: the body of a normal stomach.
Peritoneal cavity and gastrointestinal tract -141
Small and large bowel
The appearance of the bowel varies greatly depending upon the degree
of fullness. the liquid content and the amount of faeces and gas. Normal
peristalsis may be seen on scanning. If the bowel is full of fluid. there will
be characteristic mobile echoes. Peristalsis is usually seen in the small
bowel but not always in the colon.
With ultrasound. the wall of the intestine is seen as two layers: an
external hypoechogenic layer (the muscle) and an internal hyperechogenic
layer (the mucosa in contact with gas in the bowel). The muscle wall is
seldom more than 3 mm thick. depending on the part of the bowel and
the degree of filling (Fig. 87).
Fig. 87. A fluid-filled loop of small intestine.
The gas within the bowel is hyperechogenic and may produce
reverberation artefacts and an acoustic shadow posteriorly (Fig. 88).
whilejl.uid within the bowel is echo-free or may produce some echoes
due to faeces.
The normal movements due to respiration should be recognized and
differentiated from peristalsis.
Fig. 88. Reverberation artefacts and an acoustic shadow below gas in the intestine.
Intraperitoneal fluid (ascites)
Ultrasound is an accurate way of locating free
fluid in the peritoneal cavity.
The patient should lie on his or her back while the whole abdomen is
scanned, and then obliquely on the right or left side as each flank is
scanned. If there is excessive gas in the bowel, the hands/knees position
can also be used. When searching for fluid, scan the most dependent
part of the abdomen in all positions. Fluid will appear as an echo-free
area.
Small quantities of fluid will collect in two areas of the abdomen:
1. In women, in the retrouterine cul-de-sac (the pouch of Douglas)
(Fig. 89a).
2. In women and men, in the hepatorenal recess (Morrison's pouch)
(Fig. 89b).
Fig. 89a. Fluid in the pouch of Douglas (cul-de-sac) .
Fig. 89b. Transverse scan: fluid in the hepatorenal recess (Morrison's pouch).
With greater quantities of fluid, the flank spaces (parietocolic gutters)
will contain fluid. As the quantity increases, the fluid will fill the whole
of the abdominal cavity. The bowel loops will float in the fluid, bringing
the intraluminal gas close to the anterior abdominal wall, and will move
as the position of the patient changes. If the mesentery is thickened by
malignant infiltration or by infection, the bowel will be less free to move
and there will be fluid between the abdominal wall and the intestinal
loops.
:;.',;.,< ..... ,.:.-
:{Ultrasound cannot distinguish between ascites,
blood, bile, pus and urine. Aspiration is necessary
10 identify the fluid.
Peritoneal cavity and gastrointestinal tract 143
Adhesions in the peritoneal cavity cause septation. and fluid may be
obscured by intraluminal or extralumenal gas. Multiple scans in
different positions will be required.
Large cysts may simulate ascites. Scan the whole abdomen for fluid.
particularly the flanks and pelvis.
':,
helps needle aspiration of small quantities of
- but training is required (see pp. 318-319).
-
Masses in the bowel
1. Solid masses in the bowel may be neoplastic. inflammatory (e.g.
amoebic) or due to Ascaris. Bowel masses are usually kidney-
shaped. Ultrasound can show wall thickening. and an irregular.
swollen and ill-defined outline (Fig. gOa. b). Infection or spread of a
tumour may cause fixation. and associated fluid may be due to
perforation or haemorrhage. Localization may be difficult.
Fig. 90a. Transverse scan: thickened bowel wall.
Fig. 90b. Longitudinal scan of the same patient. The thickening of the bowel was
due to lymphoma. Most masses in the bowel appear kidney-shaped when imaged by
ultrasound.
When a bowel mass is identified. liver metastases must be excluded.
as well as enlarged. echo-free mesenteric lymph nodes (Fig. 90c).
Normal lymph nodes are seldom seen by ultrasound.
Fig. 9Oc. Transverse scan: enlarged abdominal lymph nodes.
2. Solid masses outside the bowel. Multiple, often confluent and
hypoechogenic masses suggest lymphoma or enlarged lymph nodes.
In children in the tropics, consider Burkitt lymphoma and scan the
kidneys and ovaries for similar tumours. However, the ultrasound
differentiation of lymphoma from tuberculous adenitis can be very
difficult (Fig. 91).
Fig. 91 a. Transverse scan: tuberculous lymph nodes. Lymphoma would have a similar
appearance.
Fig. 91 b. Retroperitoneal masses in a child due to lymphoma.
Retroperitoneal sarcoma is uncommon but may present as a large,
solid mass of varying echogenicity (see also p. 68). Necrosis may
occur centrally, appearing as a hypoechogenic or non -homogeneous
area due to liquefaction.
3. Complex masses
Abscess: may be anywhere in the abdomen or pelvis. It is often
tender, with associated fever, poorly outlined and irregular. Apart
from appendiceal abscess (see p. 147), consider:
- colonic diverticulitis with perforation: the abscess is usually in
the left lower abdomen;
- amoebiasis, with perforation: the abscess is usually in the right
lower abdomen, less often on the left side or elsewhere;
- perforation of a neoplasm: the abscess can be anywhere;
- tuberculosis or other granulomatous infections: the abscess is
commonly on the right of the abdomen, but can be anywhere;
- regional ileitis (Crohn disease), ulcerative colitis, typhoid and
other bowel infections: the abscess can be anywhere;
- perforation by parasites, e.g. Strongyloides, Ascaris or
Oesophagostomum: the abscess is usually in the right lower
abdomen, but can be anywhere. (Ascaris may be identified in
cross-section or as long, tubular structures: see p. 149).
It is often easy to identify an abscess, but it is
seldom possible to identify the cause.
A haematoma appears as a cystic or complex mass, similar to an
abscess but often apyrexial. A clinical history of recent trauma or
anticoagulant therapy is important. Haematomas may show
central debris and liquefaction, and may be loculated. Search also
for free abdominal fluid (see pp. 142-143).
4. Fluid-filled masses. The majority are benign and are either congenital
or due to parasitic or other infections. (See pp. 216-217 for
gynaecological cysts.)
Duplication of the bowel. These congenital lesions often appear as
fluid-filled variable shapes with well defined walls. They can be
large or small and may contain echoes due to debris or septations
(Fig. 92a).
Lymphatic or mesenteric cysts. Although usually echo-free, these
may be septate, with or without internal echoes. They may be
found in any part of the abdominal cavity and are variable in size,
up to 20 cm or more in diameter (Fig. 92b).
Fig. 92a. Duplication of the bowel.
Fig. 92b. An intra-abdominal lymphangioma.
5. Bowel ischaemia. Ultrasound will show solid thickening of the
bowel wall, sometimes localized but occasionally extensive. Mobile
gas bubbles may be found in the portal vein.
6. Echinococcal cysts (hydatid disease). Cysts in the abdomen have
no specific characteristics and resemble other visceral hydatid
cysts, particularly those in the liver. They are almost always
multiple, and associated with others elsewhere. (Scan the liver and
X-ray the chest.) If there are multiple small clustered cysts, suspect
the less common alveolar hydatids (Echinococcus multilocularis).
Fig. 93a. A hydatid cyst in the peritoneum with internal daughter cysts.
Fig. 93b. Multiple intraperitoneal hydatid cysts.
Fig. 93c. A mesenteric hydatid cyst with an internal daughter cyst. There is calcification in the
wall of the larger cyst.
Fig. 93d. A septate intra-abdominal hydatid cyst.
Suspected appendicitis
The diagnosis of acute appendicitis with ultrasound can be difficult and
unreliable. Considerable experience is required.
When acute appendicitis is
suspected, scan with the patient
supine, using a 5 MHz transducer.
Put a pillow under both knees to
relax the abdomen. Apply coupling
agent liberally to the right lower
abdomen and start with longitu-
dinal scans, using gentle pressure
at first. Use firmer pressure to displace the bowel. If the bowel loops are
inflamed, they will be fixed and without peristalsis: tenderness will help
localization.
An inflamed appendix appears on cross-sectional scans as fixed,
concentric circles (a "target") (Fig. 94a left). The inner lumen will be
hypoechogenic, surrounded by hyperechogenic oedema: surrounding
the oedema will be hypoechogenic bowel wall. In the long axis, the same
pattern will appear in tubular form (Fig. 94a right). If the appendix has
perforated, there will be an irregular echo-free or complex area nearby,
possibly extending into the pelvis or elsewhere (Fig. 94b).
It is not always easy to demonstrate the appendix, particularly if there
is an abscess. Other causes of an abscess in the right lower abdomen
include perforation of the bowel due to amoebiasis, neoplasm or
parasites (see p. 144). Careful correlation of the ultrasound images with
the clinical condition of the patient is essential, but it may not always
be possible to make an exact diagnosis with ultrasound.
Fig. 94a. Transverse (left) and longitudinal (right) scans of an inflamed appendix, with
thickened oedematous walls and surrounding oedema.
Fig. 94b. Transverse scan: an inflamed, ruptured appendix with resulting abscess.
Gastrointestinal symptoms in children
Ultrasound is particularly useful in the following paediatric conditions.
Hypertrophic pyloric stenosis
The diagnosis will be made clinically in the majority of infants by
palpating the olive-shaped thickening of the pylorus. This can easily be
shown by ultrasound and accurately diagnosed (Fig. 95). There will be
a hypoechogenic region due to the thickened pyloric muscle, which
should normally not exceed 4 mm. The transverse internal diameter of
the pyloric canal should not exceed 2 mm. Gastric stasis will be demon-
strated even before giving the infant the warm, sweet drink which is
necessary to fill the stomach before the rest of the examination (see
p. 138).
In longitudinal scans, the length of the pyloric canal in infancy should
not exceed 2 cm. Any measurement in excess of this strongly suggests
hypertrophic pyloric stenosis.
Fig. 95a.Transverse scan: a
normal infant pylorus.
Fig. 95b. Transverse scan:
infantile pyloric hypertrophy.
Fig. 95c. Longitudinal scan:
normal infant pylorus.
Fig. 95d. Longitudinal scan:
infantile pyloric hypertrophy.
Intussusception
When clinical examination suggests intussusception, scanning the
abdomen will sometimes demonstrate the characteristic sausage-shaped
invagination: if seen in transverse sections, the concentric rings of bowel
are also characteristic (Fig. 96a). There will be a peripheral rim which is
hypoechogenic, at least 8 mm thick and with an overall diameter of more
than 3 cm.
Fig. 96a. Transverse scan: intussusception of the bowel.
Fig. 96b. Radiograph: the barium enema of the same patient.
---,n, children, the ultrasound diagnosis of hyper-
-trophic pyloric stenQsisand intussusception
-: r'l.eeds experience and close clinical correlation.
Ascaris
Masses in any part of the bowel may be due to Ascaris: the typical
concentric rings of the bowel wall and the body of the contained worm
may be seen when scanned in transverse section. Ascaris will probably
be mobile and movement may be observed in real-time scanning.
Perforation into the peritoneal cavity may occur.
Fig. 96c. Numerous Ascaris (roundworms) in the small intestine of a child.
Infection with human immunodeficiency virus
HN-infected patients are often pyrexial, but the source of the infection
cannot always be identified by clinical examination. Ultrasound is
helpful in localizing abdominal abscesses or enlarged lymph nodes.
When there is intestinal obstruction, the dilated small bowel, with an
abnormal mucosal pattern, may be recognized early with ultrasound.
Following standard techniques, the ultrasound examination should
always include:
1. The liver.
2. The spleen.
3. Both subphrenic regions.
4. The kidneys.
5. The pelvis.
6. Any localized subcutaneous swelling or tenderness.
7. The para -aortic and pelvic lymph nodes.
Ultrasound cannot differentiate between bacterial and fungal infections.
If an abscess contains gas, it is likely to be a predominantly bacterial
infection, although mixed bacterial and fungal abscesses may occur.
When a . patient who is HIV-positive' becomes
pyrexial, abdominal and pelvic ultrasound
examination is recommended.
CHAPTER 13
Kidneys and ureters
Indications 152
Preparation 152
Normal kidney 154
Adrenal (suprarenal) glands 156
Absent kidney 157
Large kidney 158
Renal cysts 162
Renal masses 164
Small kidney 168
Renal calculi (stones) 169
Trauma 170
Perirenal fluid 171
Retroperitoneal masses 171
Suprarenal mass 171
Ureters 172
Renal differential diagnosis 173
152 Kidneys and ureters
Indications
1. Renal or ureteric pain.
2. Suspected renal mass (large kidney).
3. Non-functioning kidney on urography.
4. Haematuria.
5. Recurrent urinary infection.
6. Trauma.
7. Suspected polycystic disease.
8. Pyrexia of unknown origin or postoperative complication.
9. Renal failure of unknown origin.
10. Schistosomiasis.
;--:.' J " ~ ,- ,:
/lUltra'sound cannot assess renal function.
{ : ~ ~ ~ ; ~ : . . . ~ : . h ~
Preparation
1. Preparation of the patient. No preparation
is required. If the urinary bladder is to be
examined, the patient should drink water
(see p. 176).
2. Position of the patient. Start with the
patient lying on his/her back (supine).
Cover the right upper abdomen liberally
with coupling agent.
3. Choice of transducer. For adults, use a 3.5
MHz transducer. For children and thin
adults, use a 5.0 MHz transducer.
the transducer over the right upper
abdomen. Angle the beam as necessary and
adjust the gain to obtain the best image of
the renal parenchyma.
Scanning technique
The right kidney can be seen best with the
patient supine, using the liver as an acoustic
window.
Scanning is always done in deep suspended
inspiration: ask the patient to take a deep
breath and hold the breath in. Do not forget to
tell the patient to relax and breathe normally
again.
Start with a longitudinal scan over the right
upper abdomen and then follow with a trans-
verse scan. Next, rotate the patient to the left
lateral decubitus position, to visualize the right
kidney in this coronal view.
3.5 MHz 5 MHz
r 9
adults children
Patient holds breath in
during scanning.
y
v
left
decubitus
y
To visualize the left kidney. apply coupling agent to the left upper
abdomen. Scan the left kidney in a similar sequence.
/
/
y
v v
If the left kidney cannot be seen (usually because of excess bowel gas).
try the right decubitus position (lying on the right side).
Bowel gas can also be displaced if the patient
drinks 3 or 4 glasses of water. The left kidney
can then be visualized through the fluid-filled
stomach with the patient in the supine position.
Kidneys and ureters 153
If the kidneys have not been imaged adequately. scan through the lower
intercostal spaces. Tum the patient prone and apply coupling agent to J =-
the left and right renal area. Perform longitudinal and transverse scans
over both renal areas.
Both kidneys can also be examined with the
patient sitting or standing erect.
erect position
useful for large
patients
When examining any part of the renal area, compare both kidneys in
different projections. Variations in size, contour and internal echogenicity
rn.ay ,indicate an abnormality.
Normal kidney
Measurements made with ultrasound are generally less than those
made by radiography; they are more accurate.
Both kidneys should be about the same size. In adults. a difference of
more lhan 2 em in length is abnonnal.
1. Length: up to 12 cm and notless than 9 cm
2 . Width: normally 4-6 cm but may vary a little
with the angle of the scan
3. Thickness: up to 3.5 cm but may vary a little
with the angle of the scan
4. The central echo complex (the renal sinus)
is very echogenic and normally occupies
about one-third ofthe kidney (Fig. 97) . (The
renal sinus includes the pelvis. calyces.
vessels and fat.)
fD
f)
In the newborn. the kidneys are about 4 cm long and 2 cm wide (see
p. 287 for growth progress).
The renal pyramids are poorly defined hypoechogenic areas in the
medulla of the kidney. surrounded by the more echogenic renal cortex.
It is easier to see the pyramids in children and young adults.
length: more than 9 em,
less than 12 em
width: between 4 em and
6 em (varies with angle of
scan)
thickness: less than 3.5 em
(varies with angle of scan)
renal sinus: usually about
1/3 of the kidney
Fig. 97a. Longitudinal scan of
a normal right kidney.
Fig. 97b. Longitudinal scan of
a normal right kidney with a
bifid renal sinus.
Fig. 97c. Anterior transverse
scan through the right renal
sinus, showing the pelvis.
When scanning it is important to identifY the following:
1. The renal capsule. This appears as a bright, smooth, echogenic line
around the kidney.
2. The cortex. This is less echogenic than the liver but more echogenic
than the adjacent renal pyramids (Fig. 98a).
3. The renal medulla. This contains the hypoechogenic, renal pyramids
which should not be mistaken for renal cysts.
4. The renal sinus (the fat, the collecting system and the vessels at the
hilus). This is the innermost part of the kidney and has the greatest
echogenicity (Fig. 98b).
5. The ureters. Normal ureters are not always seen: they should be
sought where they leave the kidney at the hilus (Fig. 98c). They may
be single or multiple and are often seen in the coronal projection.
6. The renal arteries and veins. These are best seen at the hilus. They
may be multiple and may enter the kidney at different levels
(Fig. 98c).
Fig. 98a. Longitudinal scan of a normal left kidney.
Fig. 98b. Transverse scan of a normal left kidney.
Fig. 98c. Transverse scan of a normal renal sinus (renal pelvis, fat and vessels).
Adrenal (suprarenal) glands
The adrenal glands are not easily seen with
ultrasound. The best scanning positions are
with the patient supine, imaging as for the
inferior vena cava, and with the patient in the
lateral decubitus position (coronal scan). The
adrenals are situated above and medial to the
kidneys. Ifthey are easy to see, they are likely to
be pathologically enlarged, except in infants
(Fig. 99).
Fig. 99a. Longitudinal scan of the normal left adrenal gland of an infant (the adrenals are large
compared with those of an adult).
Fig. 99b. Longitudinal scan of a normal right adrenal gland of an adult.
Warning: renal pyramids may be confused with renal
cysts or tumours. Adjust the gain settings.
High Liver
Echogenicity
Spleen
Renal
cortex
Renal
medulla
Low
decubitus
Absent kidney
If either kidney cannot be seen. search again. Adjust the gain to show
the liver parenchyma and spleen. and scan in different projections.
Assess the size of the visible kidney. Hypertrophy of a kidney occurs (at
any age) in a few months when the other kidney has been removed or is
not functioning. If there is one large kidney and the other cannot be
visualized after a careful search. it is probable that the patient has only
one kidney.
If one kidney cannot be demonstrated. consider the following possibilities:
1. The kidney may have been removed. Check the clinical history and
examine the patient for scars.
2. The kidney may be ectopic. Search the kidney area and the whole
abdomen. including the pelvis (Fig. 100). If no kidney is found.
X-ray the chest. A contrast urogram may be necessary.
Fig. 100. Longitudinal scan through the bladder showing a low-lying (pelvic) kidney. The patient
is 8 weeks pregnant.
A pelvic kidney may be confused sonographically
with a tubo-ovarian mass or gastrointestinal tumour.
Use a contrast urogram to locate the kidney.
3. If only one large but normal kidney is demonstrated. and there has
not been any surgery. it is likely that there is congenital absence of
the other kidney. If the only kidney visualized is not enlarged. a
failure to demonstrate the other kidney suggests chronic disease.
4. If there is one large but distorted kidney. there may be a developmental
abnormality.
5. Apparent absence of both kidneys may be a failure to demonstrate
them with ultrasound because of changed echogenicity resulting
from chronic disease of the renal parenchyma.
6. Any kidney less than 2 cm thick and 4 cm long can be very difficult
to visualize. Locate a renal vessel or ureter; this may help to localize
the kidney. especially if the ureter is dilated.
Large kidney
Bilateral enlargement
1. When the kidneys are enlarged but nonnal in shape. with nonnal.
decreased or increased homogeneous echogenicity. the possible
causes are:
Acute or subacute glomerulonephritis or severe pyelonephritis
(Fig. 10 1 a).
Amyloidosis (probably increased echogenicity) (Fig. 101b).
The nephrotic syndrome.
Fig. 101 a. Longitudinal scan: a large kidney due to glomerulonephritis. (Size must always be
confirmed by measurement.)
Fig. 101 b. Two longitudinal scans: enlarged hyperechogenic kidneys in two patients with
amyloidosis. The differentiation between renal cortex and sinus is no longer so clearly visible.
2. When the kidneys have a smooth outline and are unifonnly enlarged.
with non-homogeneous hyperechogenicity. the possible causes are:
Lymphoma. This may cause multiple areas oflow density, especially
Burkitt lymphoma in children or young adults (Fig. 102).
Metastases (Fig. 102).
Polycystic kidneys (see p. 162).
Fig. 102. Longitudinal scans: on the left. the renal tissue has been partially replaced by Burkitt
lymphoma; on the right. by metastases.
Unilateral enlargement
If one kidney appears to be enlarged but has nonnal echogenicity, and
the other kidney is small or absent, the enlargement may be due to
compensatory hypertrophy. When no other kidney is seen, exclude
crossed ectopia and other developmental abnonnality (Fig. l03a, b).
The kidney may be slightly enlarged because of
persistent segmentation (duplication) with two
or even three ureters. Search for the renal hilus:
there are likely to be two or more vessels and
ureters. A contrast urogram may be necessary.
Fig. 103a. Longitudinal scan: an unobstructed duplex kidney.
Fig. 103b. Longitudinal posterior scan: an obstructed (hydronephrotic) duplex left kidney.
Fig. 103c. Longitudinal scan: crossed fused renal ectopia.
One kidney is enlarged or more lobulated than normal
The commonest cause of an enlarged kidney is hydronephrosis, which
will appear on ultrasound images as multiple, well circumscribed cystic
areas (the calyces) with a dilated central cystic area (the renal pelvis,
normally less than 1 cm in width). Coronal images will show the
continuity between the calyces and the pelvis. In multicystic kidneys
there is no such continuity (see p. 162).
Fig. 104a. Longitudinal scan: the renal pelvis of a normal kidney is less than 1 cm in width.
Fig. 104b. Longitudinal scan: a renal pelvis more than 1 cm in width, indicating mild
hydronephrosis. Small parapelvic cysts have a similar appearance.
Fig. 104c. Longitudinal scan: calyceal dilatation, indicating moderate hydronephrosis.
Fig. 104d. Longitudinal scan: dilated calyces and a renal cortex decreased in width are
indicative of advanced hydronephrosis.
Degrees of
hydronephrosis
Normal
Mild
Moderate
Severe
d
ex
calyx
Always compare the two kidneys when assessing the size of the renal
pelvis. When much of the pelvis is outside the renal parenchyma, it may
be a normal variant. When the renal pelvis is enlarged, normal echoes
can be lost because of the fluid content (Fig. 105a).
Fig. 105a. Longitudinal (upper) and transverse (lower) scans: a kidney with a large extrarenal
pelvis.
A large renal pelvis may be due either to overhydration with increased
urinary output or to an overfilled urinary bladder. The renal calyces will
be normal. Ask the patient to empty the bladder and res can (Fig. 105b).
Pelvic dilatation can occur normally in pregnancy and does not necessarily
indicate infection. Check the urine for infection, and check the uterus
for pregnancy.
Fig. 105b. Dilated calyces due to overhydration (left) which become normal after micturition
(right).
A large renal pelvis is an indication to scan the ureters and the bladder
and particularly the other kidney to locate the obstruction. If no cause
is identified, a contrast urogram will be necessary. The normal con-
cave calyces may become inverted and rounded as the degree of ob-
struction increases. Eventually the renal cortex becomes thinned (see
p. 160).
To assess the degree of hydronephrosis, measure the size of the renal
pelvis when the bladder is empty. If the pelvis is wider than 1 cm, but
there is no calyceal dilatation, the hydronephrosis is mild. When there
is calyceal dilatation, the hydronephrosis is moderate. If there is loss of
the renal cortex, it is advanced (Fig. 104).
Hydronephrosis can be caused by congenital obstruction of the uretero-
pelvic junction, by ureteric stenosis (e.g. as in schistosomiasis
(Fig. 122c, p. 179)) or a calculus, or from external pressure on the
ureters by a retroperitoneal or abdominal mass.
LARGE RENAL
PELVIS
Scan the
uterus
(pregnant?)
LARGE RENAL
PELVIS
Scan ureters,
bladder, other
kidney
Renal cysts
When ultrasound shows multiple, echo-free, well circumscribed areas
throughout the kidney, suspect multicystic kidney. This condition is
usually Unilateral, whereas congenital polycystic kidney disease is
almost always bilateral (although the cysts may not be symmetrical)
(Fig. 106a).
Internal
echoes Back wall Contour Shape
Cyst No Strong Well defined Spherical
Tumour Yes No change Irregular Variable
or strong III defined
1. Simple cysts can be single or multiple. On ultrasound the walls are
smooth and rounded without internal echoes, but with a clearly
defined back wall (Fig. 106b, c). Such cysts are usually unilocular
and, when multiple, will differ in size. Rarely, these cysts become
infected or haemorrhage, producing internal echoes. When this
occurs or when the outline of any cyst is irregular, further investigation
is required.
Fig. 106a. Longitudinal scan:
multicystic right kidney. All the
cysts are approximately the
same size.
Fig. 106b. Longitudinal scan:
a large single cyst in the right
kidney.
multiple renal cysts.
More than 70% of all renal cysts are due to benign cystic disease. These cysts
are very common over .the age of 50 years and maybe bilateral. They seldom
cause symptoms.
2. Hydatid cysts usually contain debris and
are often loculated or septate (Fig. 107a, b).
When calcified, the wall appears as a bright,
echogenic convex line with acoustic
shadowing (Fig. 107c). Hydatid cysts may
be multiple or bilateral. Scan the liver for
other cysts and X-ray the chest.
Fig.107a. Longitudinal scan: a hydatid cyst in a right kidney.
Fig. 107b. Transverse scan: a septate hydatid cyst in a right kidney.
Fig. 107c. Supine longitudinal scan: a collapsed calcified hydatid cyst in the upper pole of a left
kidney.
3. If there are multiple cysts in one kidney, the kidney is usually
enlarged. This may indicate alveolar echinococcosis. If the patient
is less than 50 years old and clinically well. check the other kidney
to exclude polycystic disease: congeniial cysts are echo-free and
without mural calcification. Both kidneys are always enlarged
(see p. 162).
Renal masses
Ultrasound cannot reliably differentiate between
benign renal tumours (other than renal cysts)
and malignant renal tumours, and cannot always
accurately differentiate malignant tumours from
renal abscesses.
There are two exceptions to the above statement:
1. In the early stages, a renal angiomyolipoma (Fig. 1 08a) has ultrasound
characteristics that allow accurate recognition. These tumours can
occur at any age and may be bilateral. Ultrasound images show a
well Circumscribed, hyperechogenic and homogeneous mass, and
as the tumour grows there will be back wall attenuation. However,
some tumours will undergo central necrosis and there will be strong
back wall echoes. At this stage differentiation by ultrasound is no
longer possible, but abdominal X-rays may show fat within the
tumour, which is unlikely to occur in any other type of renal mass.
Fig.108a. Supine longitudinal scan: an angiomyolipoma in a right kidney.
2. When a renal tumour spreads into the inferior vena cava or into the
perirenal tissues, there is no doubt that the tumour is malignant
(Fig. 108b). (See also p. 166.)
Fig. 108b. Longitudinal scan: a large renal tumour involving the inferior vena cava and
spreading beyond the renal capsule.
Solid renal mass
Renal masses may be well circumscribed or irregular and may alter the
shape of the kidney. Echogenicity may be increased or decreased. In the
early stages. the majority of malignant tumours are homogeneous: if
central necrosis occurs. they become non-homogeneous (Fig. 1 09a. b. c).
Fig. 109a. Oblique longitudinal scan: a well-circumscribed tumour in a right kidney.
Fig. 109b. Oblique longitudinal scan: an irregular. ill-defined tumour in a right kidney.
Fig.109c. Longitudinal scan: a tumour with central necrosis in a right kidney.
It is important to recognize normal or hypertrophied columns of Bertin. which can
resemble a tumour (Fig. 110). The echo pattern of the cortex should be the same
as the rest of the kidney; however. in some patients. differentiation may be
difficult.
Fig. 110. Transverse scan: a normal prominent column of Bertin.
A complex non-homogeneous mass
The differential diagnosis of complex masses can be very difficult, but
when there is spread of a tumour beyond the kidney, there is no doubt
that it is malignant (Fig. lIla, b). Malignant tumours may also be
contained within the kidney (see p. 165). Both tumours and haematomas
may show acoustic shadowing due to calcification.
Fig. 111a. Longitudinal scan: a tumour in a left kidney, which is invading the renal tissue and
beyond it (renal carcinoma) .
Fig. 111 b. Transverse scan: a tumour in the lower pole of a left kidney, invading the left ureter
and causing obstructive hydronephrosis.
As a tumour grows, its centre may become necrotic with a rough
irregular outline and much internal debris, causing a complex ultrasound
pattern. The differentiation ofthis from an abscess or a haem atom a can
be difficult. The clinical condition of the patient may indicate the correct
diagnosis. Tumours can spread into the renal vein or inferior vena cava
and resemble thrombosis (Fig. lllc) (see p. 69).
Fig. 111 c. Longitudinal scan: a renal tumour invading the renal vein and inferior vena cava,
resulting in thrombosis.
Always scan both kidneys. When a maligr)ant" e n ~ l
tumour is suspected (at any age), scan the liver and the
inferior vena cava. Also X-ray the chest for metastases.
A rough, irregular, echogenic mass containing debris within an en-
larged kidney may be malignant or a pyogenic or tuberculous abscess
(Fig. 112a, b, c). The patient's clinical condition may help to differentiate
(see also p. 166).
Fig. 112a. Transverse scan: a centrally necrotic renal tumour with internal debris.
Fig. 112b. Longitudinal scan: a large pyogenic abscess, seen as a complex mass in the right kidney.
Fig. 112c. Longitudinal scan: a tuberculous abscess in the right kidney.
In . children,malignal'lt tUTours, e.g.
tumour), may be well encapsulated but not
showcalcjticati9n but not in the capsule.
may change the echogenicity;(Fig. ,112d); .$ome.are:bilateraL::y!"'
. :'. ..:" . " - .' -c: ",::::' ':.- '. :r:;:t):':: .. '"
. -.:.'(:,.,:
Fig. 112d. Longitudinal scan: a Wilms tumour in the right kidney of a child showing nodularity
and areas of necrosis.
Small kidney
1. A small kidney with nonnal echogenicity may be due to renal artery
stenosis or occlusion, or to congenital hypoplasia (Fig. 1I3a).
Fig. 113a. Longitudinal scan: a small, isodense but otherwise normal left kidney: the result of
renal artery stenosis.
2. A small kidney, nonnal in shape but hyperechogenic, may indicate
chronic renal disease (Fig. 1I3b). In renal failure, both kidneys are
likely to be equally affected.
Fig. 113b. Longitudinal scan: a small right kidney, associated with chronic renal failure.
3. A small, hyperechogenic kidney with an irregular, rather "rough"
outline and variable thickness of the cortex (usually bilateral but
often very asymmetrical) is probably the result of chronic
pyelonephritis or infection such as tuberculosis. There may be
calcification in the abscesses, showing as bright areas (Fig. 1I3c).
Fig. 113c. Longitudinal scan: a small, irregular (scarred) kidney, the result of chronic
pyelonephritis.
4. A single, small, nonnally shaped but hyperechogenic kidney may be
due to end-stage renal vein thrombosis. Acute renal vein thrombosis
usually causes renal enlargement, with shrinkage occurring later.
Chronic obstructive nephropathy can affect one kidney in the same
way, but chronic glomerulonephritis is usually bilateral.
Renal calculi (stones)
Not all calculi can be seen on a plain radiograph of the abdomen, and
not all renal calculi can be detected by ultrasound. If clinical symptoms
suggest calculi, all patients with a negative ultrasound examination
need intravenous contrast urography.
Suspected urinary calculi, urine abnormal but negative
ultrasound = intravenous urography.
Calculi are most easily seen in the renal collecting system. The minimum
detectable size on a general purpose ultrasound unit, using a 3.5 MHz
transducer, is 3-4 mm diameter. Smaller stones (2-3 mm) may be seen
with a 5 MHz transducer. A calculus will be hyperechogenic with an
acoustic shadow (Fig. 114). The calculus must be visualized in two
different planes, longitudinal and transverse, to permit accurate
localization and measurement. This may avoid confusion with calcification
in the renal parenchyma and other tissues, e.g. the neck of a calyx,
which can simulate calculus and give a similar echo and shadow.
Fig. 114a. Longitudinal scan: a calculus in a right kidney.
Fig. 114b. Longitudinal scan: multiple calculi in a right kidney.
r ~ t e r i c calculi are very difficult tolocate by ultrasound.
Failure to see a ureteric calculus does not mean that
there is no calculus.
5MHz
transducer
170. Kidneys and ureters
Trauma
1. In the acute stage, renal ultrasound may show intrarenal or
perirenal echo-free areas as a result of the presence of blood
(haematoma) or extravasated urine (Fig. l15a, b).
Fig. 115a. Longitudinal scan of an injured patient: the lower pole of the left kidney has been
ruptured and there is fluid (blood or urine) around the left kidney.
Fig. 115b. Longitudinal scan: fluid around the kidney following injury.
2. When the blood has clotted and formed a thrombus, the same areas
will show as bright echoes or a mixture of echo and echo-free areas
(a complex mass or masses) (Fig. l15c). In all cases of trauma, check
the opposite kidney, but remember that ultrasound cannot assess
renal function.
Fig. 115c. Transverse scan: clotted blood around the right kidney, following injury.
Ability to visualize the kidney does not mean that it is
functioning. To assess renal function, use contrast
urography, a radionuclide study or laboratory tests.
Remember that injury to a kidney may result in
temporary loss of function.
Perirenal fluid
Blood, pus and urine around the kidney cannot be distinguished on
ultrasound. All appear as an echo-free area (Fig. 116) (see also p. 170).
Fig. 116. Transverse scan: a left perirenal abscess.
Retroperitoneal masses
Lymphoma usually presents as a hypoechogenic para-aortic or aorto-
caval mass. If the gain is set too low, it may resemble fluid. Any such
mass can displace the kidney.
A psoas abscess or haematoma can be echo-free or complex: clotted
blood will be hyperechogenic. If there is gas, some areas may be
hyperechogenic with acoustic shadows (Fig. 117).
Fig. 117. A large retroperitoneal (psoas) abscess.
Suprarenal mass
Scan both adrenals. A suprarenal mass may be a primary or metastatic
tumour, abscess or haematoma. Most are well defined but may become
complex. Adrenal haemorrhage is common in the newborn (Fig. 118).
Fig. 118. Longitudinal scan: benign adenoma of the right adrenal gland.
Kidneys and ureters -171
Failure to see an adrenal gland does not exclude abnormality.
Ureters
Because of their position behind the bowel. it is not easy to examine
normal ureters by ultrasound. If dilated (e.g. by outlet obstruction due
to an enlarged prostate or urethral stricture, or due to vesico-ureteric
reflux), they are easier to see, particularly near the kidney or bladder.
The middle of the ureters is never seen easily and is much better
demonstrated by intravenous urography. However, if thickened, as in
schistosomiasis (sometimes with calcification), they can be recognized
with ultrasound (Fig. 119) (see also p. 179).
The lower end of the ureters can be observed by scanning through a full
bladder, which provides a useful acoustic window.
Fig. 119a. Dilatation of the lower end of the right ureter, caused by a calculus.
Fig. 119b. Transverse scan: a large calculus at the lower end of the ureter. Small ureteric
calculi may be difficult to localize with ultrasound scanning.
Fig. 119c. Longitudinal scan through the full bladder, showing thickening and dilatation of the
lower end of the ureter in a child with schistosomiasis. (Ultrasound scanning is a useful way to
monitor treatment of this infection and to differentiate calcification from artefacts.)
"'i y: - _ .. .::....- ';
-way to
-.' .. '::'"
._ ... .. " '. . . , .. _,\ . :
Renal differential diagnosis
A single large cyst
Exclude gross hydronephrosis.
Irregular renal outline (not lobulated)
Consider chronic pyelonephritis or
multiple renal infarcts.
Irregular renal outline (smooth)
. Normal lobulation or cystic disease
(congenital or parasitic).
Missing kidney
Ectopia or displacement..
Surgery.
Too small to see on ultrasound.
Replacement by tumour.
Large kidney (normal shape)
Hydronephrosis.
Cystic disease.
Acute renal vein thrombosis.
Compensatory hypertrophy (other kidney
absent or diseased).
Large kidney (asymmetrical shape)
Tumour.
Abscess.
Hydatid cyst.
Adult polycystic disease.
Small kidney
Glomerulonephritis.
Chronic pyelonephritis.
Infarction or chronic renal vein
thrombosis.
Congenital hypoplasia.
Perirenal fluid"
Blood.
Pus.
Urine.
*Ultrasound cannot distinguish
the type oj fluid.
Missing kidney? Always check the opposite
kidney and in the pelvis.
174
Notes
CHAPTER 14
Urinary bladder
Indications 176
Preparation 176
Normal bladder 177
Abnormal bladder 178
176 Urinary bladder
Indications
1. Dysuria or frequency of micturition.
2. Haematuria (wait until bleeding has stopped).
3. Recurrent infection (cystitis) in adults; acute infection in children.
4. Pelvic mass.
5. Retention of urine.
6. Pelvic pain.
, ,-
- y -
. -Always scan both k i ~ n y s when examining' the
. bladder.
Preparation
l. Preparation of the patient. The bladder must be full. Give 4 or 5
glasses of fluid and examine after one hour (do not allow the patient
to micturate). Alternatively, fill the bladder through a urethral
catheter with sterile normal saline: stop when the patient feels
uncomfortable. Avoid catheterization if possible because of the risk
of infection.
lie supine but may need to be rotated
obliquely.
The patient should be relaxed, lying
comfortably and breathing quietly.
Lubricate the lower abdomen with coupling
agent. Hair anywhere on the abdomen will
trap air bubbles so apply coupling agent
generously.
Scanning technique
Start with transverse scans from the pubic
symphysis upwards to the umbilicus. Follow
with longitudinal scans, moving from one side of
the lower abdomen to the other.
These scans will usually be sufficient, but it is
not always easy to see the position of the lateral
and anterior walls of the bladder and patients
may have to be turned 30-45 to see an area
more clearly. Any area that appears abnormal
must be viewed in several projections. After
scanning, the patient should empty the bladder
and should then be rescanned.
~
.. :'?: .... ,
........... ,
........... ,
+ ... ...... .
-<- ,
~ ..
V
3.5 MHz
adults
1 litre
5MHz
children
Normal bladder
The full urinary bladder appears as a large. echo-free area arising out
of the pelvis. Start by assessing the smoothness ofthe interior wall ofthe
bladder and its symmetry in transverse section. The thickness of the
bladder wall will vary with the degree of distention but should always be
approximately the same all around the bladder. Any local area of
thickening is abnormal. Look also for trabeculation (see pp. 178-179).
When distended. the normal bladder wall is less than 4 mm thick.
Mter scanning. the patient should empty the
bladder (Fig. 120c). Normally. there should be
no residual urine: if there is. the quantity should
be estimated. Measure the transverse diameter
(T) of the bladder in centimetres. multiply it by
the longitudinal diameter (L) in centimetres and
then by theAP diameter in centimetres. Multiply
the total by 0.52. This measures the residual
urine in millilitres (cubic centimetres).
Urinary bladder -177
full bladder: wall less
than 4 mm thick
L
When the bladder has been thoroughly
examined. scan the kidneys and the ureters (see
Chapter 13).
T x Lx AP x 0.52 = volume (ml)
Fig. 120a. Longitudinal scan: normal full bladder.
Fig. 120b. Transverse scan: normal full bladder.
Fig. 120c. Transverse scan: normal empty bladder.
178 Urinary bladder
Abnormal bladder
It is important to scan for:
1. Variation of the bladder wall thickness and
trabeculation.
2. Asymmetry of the bladder.
3. Cystic masses in or outside the bladder
(ureterocele or diverticulum).
4. Solid masses within the bladder or at the base
of the bladder.
For differential diagnosis, see pp. 182-183.
Generalized thickening of the bladder wall
3
1. In men, bladder wall thickening is usually the result of prostatic
obstruction (Fig. 121a). If suspected, check the prostate (Fig. 124c,
p. 183): exclude hydronephrosis by scanning the ureter and the
kidneys. Search for associated diverticula: these project outwards
but are only visible if over 1 cm in diameter. Diverticula are usually
echo-free with good sound transmission (Fig. 121 b). Sometimes the
opening of a diverticulum can be demonstrated: diverticula may
collapse or increase in size after micturition.
2. Severe, chronic infection/ cystitis. The inner wall of the bladder may
be thickened and irregular (Fig. 121c). Check the rest of the renal
tract for dilatation.
Fig. 121 a. Hypertrophy of the wall of the bladder.
Fig. 121 b. Longitudinal scan: diverticulum of the bladder.
Fig. 121 c. Chronic bladder infection (chronic cystitis).
3. Schistosomiasis. The bladder walls may be thickened. with increased
echogenicity and scattered dense (bright) areas due to calcification
(Fig. 122a. b). The calcification varies and may be throughout
or patchy. and differing in thickness. The calcification is in the
intramural ova and does not prevent normal contraction of the
bladder.
Poor bladder emptying indicates superimposed active infection. or
prolonged or recurrent infection. The extent of the calcification does
not indicate the activity of the schistosomal infection. and calcification
may decrease in the later stages. However. the bladder wall usually
remains thickened and does not easily distend. There may also be
hydronephrosis (Fig. 122c).
4. Very thick trabeculated bladder walls in children may result from
outlet obstruction caused by urethral valves or urogenital diaphragm.
5. A thickened bladder wall may occur in a neurogenic bladder and will
usually be associated with uretero-hydronephrosis.
Urinary bladder 179
Fig. 122a. Two transverse
scans showing thickening and
irregularity of the bladder wall
of a 12-year-old child with
schistosomiasis. The left
ureter is also thickened
(lower).
marked polypoid mucosal
thickening and patchy
calcification in the bladder of
an 8-year-old child with
schistosomiasis.
hydronephrosis and
hydroureter caused by
schistosomiasis. There is also
sludge in the renal pelvis as a
result of associated urinary
tract infection.
180 Urinary bladder
Localized thickening of the bladder wall
Whenever localized bladder wall thickening is
suspected, multidirectional scans are needed,
particularly to exclude a polyp. Moving the
patient or increasing the volume of fluid in the
bladder will help to identify bladder folds. (Folds
will disappear as the bladder distends.) If there
is any doubt, repeat after 1 or 2 hours: do not let
the patient micturate before the examination is
repeated (Fig. 123a, b).

CP
Thick bladder wall?
More fluid.
Fig. 123a. Longitudinal scan: apparent thickening with folds in the wall of a partially filled
bladder.
Fig. 123b. Transverse scan of the same patient. The bladder is now distended and the thick
folds have disappeared.
Localized thickening may be due to:
1. Bladder fold due to incomplete filling (Fig. 123 a, b).
2. Tumour: sessile or polypoid, single or multiple (Fig. 123c, d, e).
3. Localized infection due to tuberculosiS or to schistosomal plaques
(granulomas) (Fig. 122a, c, p. 179).
4. Acute reaction to schistosomal infection in children.
5. Haematoma following trauma (Fig. 1231).
Fig. 123c. A sessile polyp in the bladder: longitudinal (left) and transverse (right) scans.
Fig. 123d. Transverse scan: pseudotumour in the bladder, caused by blood clots.
Fig. 123e. Transverse scan: a large malignant tumour arising from the bladder wall.
Fig. 123f. Transverse scan: following injury, there is blood lateral to the bladder, distorting and
apparently thickening the bladder wall.
182 Urinary bladder
Differential diagnosis of localized bladder wall thickening
1. Most bladder neoplasms are multiple but located in one area. Some
only thicken the bladder wall, but most are also polypoid. It is
essential to recognize when the tumour has spread through the
bladder wall. Calcification in the tumour or wall due to associated
schistosomiasis may cause bright echoes (Fig. 122 and 123, pp. 179
and 181).
2. Bladder polyps are often mobile on a stalk, but some, especially
those due to infection, may be sessile and not easily differentiated
from a malignant tumour (Fig. 123c, p. 181).
3. Granulomas (e.g. tuberculous) cause multifocal but localized
thickening. The bladder is often small and becomes painful when
distended, resulting in frequent micturition: in malignancy, bladder
distention is painless. Schistosomiasis may cause multiple flat
plaques and polyps (Fig. 122. p. 179). Any chronic infection will
eventually decrease bladder capacity (see p. 186).
4. Trauma. If there is localized thickening following trauma. scan the
pelvis to exclude fluid (blood or urine) outside the bladder (Fig. 123f.
p. 181). Repeat the scan after 10-14 days. If the thickening is due
to a haematoma. the swelling should have decreased.
5. Schistosomiasis. Children who are reinfected can have an acute
"urticarial" reaction in the bladder wall causing marked local
thickening of the bladder mucosa. This subsides with treatment or
spontaneously over a few weeks (Fig. 122a. p. 179).
Blood clot and tumour look alike, and both may be
associated with haematuria.
Density within the bladder
1. Attached to the wall
Polyp. A polyp on a long stalk may appear freely mobile. Change
the patient's position and rescan.
Adherent calculus. Calculi can be single or mUltiple, small or
large: they usually have acoustic shadowing. Some may become
adherent to the bladder mucosa. especially when there is infection:
scan with the patient in different positions to assess movement
(Fig. 124a) (see also p. 184).
Fig. 124a. Transverse scan: a single large calculus adherent to the bladder wall.
Ureterocele. A ureterocele presents as a cystic mass within the
bladder, near a uretertc ortfice (Fig. 124b). It will change in size if
scanned at different times. In children, the ureterocele may be so
large that the opposite ureter is also obstructed. Ureteroceles are
sometimes bilateral but are seldom symmetrtcal. If suspected,
scan the kidneys and the ureters for asymmetrtcal hydronephrosis
and hydroureter, and for duplication of the ureters (p. 159).
Enlarged prostate. An echogenic, non -mobile mass located centrally
at the base of the bladder in a male patient is most likely an
enlarged prostate (Fig. 124c). In women, an enlarged uterus can
also distort the bladder (Fig. 124d).
Fig. 124b. Transverse scan: a prominent ureterocele.
Fig. 124c. Longitudinal scan: a markedly enlarged prostate.
Fig. 124d. Transverse scan: distortion of the bladder wall by pressure from a large uterine
myoma.
184 Urinary bladder
2. Mobile density within the bladder
Calculus. Unless they are very large. most calculi move within the
bladder (Fig. 125a). However. calculi may be trapped in a
diverticulum or be so large that they seem to fill the bladder: the
capacity of the bladder to hold urine will be reduced when there
is a large stone. When there is doubt about a bladder calculus.
change the position of the patient and rescan. Most small and
medium-size calculi will change position. but a large calculus may
not be able to move (Fig. 124a. p. 182).
Foreign body. Catheters must be recognized (Fig. 125b). Very
rarely a foreign body is introduced into the bladder. If this is
suspected. a careful history is necessary: X-rays may be helpful.
Blood clot. A thrombus can resemble a calculus or a foreign body:
not all blood clots are freely mobile (Fig. 125c).
Air. Introduced into the bladder either through a catheter or by
infection or through a fistula. air appears as an echogenic. mobile.
non-dependent (floating) area.
Fig. 125a. Transverse scan: multiple calculi in the bladder.
Fig. 125b. Longitudinal scan: the balloon of a Foley catheter next to the bladder wall.
Fig. 125c. Transverse scan: a large. laminated blood clot in the bladder.
Large (overdistended) bladder
When distended, the bladder walls will be smooth and evenly stretched,
with or without diverticula Use measurements to confirm suspected
overdistension (Fig. 126a, b).
Always look at the ureters and check the kidneys for hydronephrosis.
Ask the patient to empty the bladder and rescan to see ifit is completely
empty (Fig. 126c).
Common causes of bladder distention are:
1. Enlargement of the prostate.
2. Urethral stricture in the male.
3. Urethral calculus in the male.
4. Bruising of the urethra in the female ("honeymoon urethritis").
5. A neurogenic bladder from damage to the spinal cord.
6. Urethral valves or diaphragm in newborn infants.
7. Cystocele in some patients.
Fig. 126a. Normal full bladder and measurements: transverse scan (left) and longitudinal scan
(right). Volume (ml) = T x L x AP x 0.52
Fig. 126b. Longitudinal scan: an overdistended bladder.
Fig. 126c. Transverse scan: a large quantity of residual urine after micturition. (Compare empty
bladder, Fig. 120c, p. 177).
Urinary bladder 185
186 Urinary bladder
Small bladder
A bladder may be small because of cystitis.
which prevents the patient from holding urine
and causes a clinical history of frequent and
painful micturition. The bladder may also be
small because the walls have been damaged
or fibrosed. reducing the bladder capacity
(Fig. 127). Micturition will then be frequent but
not painful.
If there is any doubt. give the patient more fluid
and ask him or her not to micturate; rescan in
1-2 hours.
--I
-
Thick. irregular
bladder wall
Small bladder?
More fluid
. " -\--
' .... J
Thick, i rreg ular
bladder wall
Fig. 127. Longitudinal scans in different planes: the bladder is small and irregular as a result of
fibrosis. It did not distend any further, even after the patient had drunk more fluid.
A small bladder may be due to:
1. Late schistosomiasis. There may be bright echoes due to calcification
(see p. 179).
2. Recurrent cystitis. particularly due to tuberculosis. Bladder wall
thickening is likely (Fig. 121c. p. 178).
3. The rare infiltrating neoplasm. When there is a tumour. the bladder
wall is nearly always asymmetrical (see p. 182).
4. Radiotherapy or surgery for malignancy. Check the clinical history.
Always ask the patient to drink more fluid and
rescan in 1-2 hours before diagnosing a small
bladder.
- ------
CHAPTER 15
Scrotum and testis
Indications 188
Preparation 188
The normal testis 189
Abnormal scrotum 190
The epididymis 192
Trauma 193
Hernia 194
Varicocele 194
188 Scrotum and testis
Indications
1. Swelling of the scrotum.
2. Trauma.
3. Infection.
4. Pain.
5. Apparently absent testicle (swelling in the groin in young males).
6. Haematospermia.
7. Infertility.
Preparation
1. Preparation of the patient. No preparation is required.
2. Position of the patient. The patient should be supine. Lift the penis
upwards towards the abdomen and cover with a towel.
Apply coupling agent liberally to cover the scrotum.
3. Choice of transducer. If available. a 7.5 MHz sector transducer is
preferable. especially for children. Otherwise. use a 5 MHz transducer.
Scanning technique
Scan both testes from different angles. Compare the testes at each
projection.
7.5 MHz 5 MHz
The normal testis
The normal testis is oval, homogeneous and
hyperechogenic (Fig. 128a, b) .
1. The average length in the adult is 5.0 cm.
2. The average width is 3.0 cm.
3. The average transverse diameter is 2.0 cm.
4. The vertical diameter is 2.5 cm.
The epididymis lies on the inferior aspect of the
testis and is more echogenic than the testis. It is
subdivided into a head, body and tail, the head
being the part most reliably demonstrated by
ultrasound (Fig. 128c).
~ 2 5 C m
\!:t2.0cm
The two testes are separated in the scrotum by a hyperechogenic
septum. There are often small collections of fluid within the scrotum.
Fig. 128a. Longitudinal scan: normal testis. The fibrous testicular mediastinum can be
identified.
Fig. 128b. Transverse scan: normal testis.
Fig.128c. Normal epididymis and scrotum.
Scrotum and testis 189
Abnormal scrotum
Unilateral swelling
Swelling on one side of the scrotum may be due to:
1. Hydrocele. Fluid in the scrotum will surround the testis with an
echo-free region, varying in size and position (Fig. 129). If the fluid
is due to inflammation or trauma, there may be internal debris
causing internal echoes on ultrasound. The testis must be carefully
examined to exclude underlying malignancy (Fig. 130).
Fig. 129a. Longitudinal scan: a small hydrocele.
Fig.129b. Longitudinal scan: a moderate hydrocele.
Fig.129c. Transverse scan: a large hydrocele. The scrotal wall is thickened by oedema.
2. Trauma and torsion of the testis (see p. 193).
3. Hernia (see p. 194).
4. Varicocele (see p. 194).
------------------ --
5. Testicular mass, e.g. tumour or infection. The majority oftesticular
tumours are malignant. The tumours may be hypoechogenic or
hyperechogenic, and the testis may be normal in size or enlarged.
The two testes must be compared, because a tumour may replace
all the normal tissue, and can then only be recognized by the
difference in echogenicity. Even when the two testes are of equal
density, gentle compression may show a small tumour not
demonstrated by routine scanning (Fig. 130a, b). It can be difficult
to distinguish between tumour and infection (Fig 130c).
Fig.130a. Transverse scans: the right testis is normal; the left testis is hypoechogenic. This
could be because of infection or oedema associated with a small tumour. There is a bilateral
hydrocele, the left larger than the right.
Fig. 130b. Left: seminoma of the right testis. Right: mixed germ cell tumour (choriocarcinoma)
of the left testis with areas of necrosis.
Fig. 130c. Longitudinal scan: a tuberculous abscess of the testis.
Small or absent testis
Failure to demonstrate a testis in the scrotum with ultrasound indicates
that the testis is absent. If clinical examination of the inguinal canal
reveals a mass, ultrasound can demonstrate the location and size of the
mass, but may not be able to differentiate testicular tissue from an
enlarged lymph node. Ifthere is no palpable mass in the inguinal region
on clinical examination, there is no indication to proceed with ultrasound.
The epididymis
The epididymis may become infected or develop cysts.
l. Epididymitis. Ultrasound will demonstrate an enlarged and
hypoechogenic epididymis on the affected side. If there is associated
orchitis, the testis will also be comparatively hypoechogenic
(Fig. 131a, b). Chronic epididymitis may have both hypo- and
hyperechogenic areas (Fig. 131c.)
Fig. 131a. Transverse scan: acute epididymitis.
Fig. 131 b. Moderate epididymo-orchitis; both the epididymis and the testis are hypoechogenic
and swollen. There is a hyd' die.
Fig. 131 c. Chronic epididymitis. There are hypoechogenic and hyperechogenic areas.
2. Cyst in the epididymis. Cysts may be single or multiple, and are
confined to the epididymis. The testis will not be affected. Epididymal
cysts must be differentiated from the more tubular varicocele (see
p.194).
Trauma
Following injury, the testis may be enlarged or remain normal in size.
When there is excess fluid in the scrotum, the testis should be scanned
at many diferent angles to exclude rupture. The injured testis may show
complex echogenicity, especially when there is an internal haematoma
(or subsequent abscess). Blood will appear as fluid within the scrotum,
often with complex echogenicity due to blood clots (Fig. 132a, b).
Torsion of the testis
It may be difficult to confirm torsion of the testis with ultrasound, but
if the rotation has disrupted the normal blood supply, ultrasound will
demonstrate decreased echogenicity, compared with the normal testis,
in the acute stage (Fig. 132c}. There may be associated scrotal fluid
(hydrocele) (see also p. 190).
Fig. 132a. Longitudinal scan: a haematoma of the testis without disruption (fracture) but with a
small haematocele.
Fig. 132b. Transverse scan. Shattered and swollen right testis, with compression of the left
testis. There is a small haematocele.
Fig. 132c. Longitudinal scan: torsion of the testis, confirmed surgically. The testis has
decreased echogenicity.
Hernia
Omenta, mesentery or intestinal loops that have prolapsed through an
inguinal hernia into the scrotum are usually associated with a small
hydrocele. The loops of bowel will appear on ultrasound as a complex
mass within the echo-free fluid. If there is a significant solid content
within the bowel, there will be hyperechogenic areas also (Fig. 133).
Fig. 133. Longitudinal scan: a small inguinal hernia in a young, healthy male.
Varicocele
When the veins draining the testis and epididymis are dilated, ultrasound
will demonstrate multiple tortuous, tubular, hypoechogenic structures
around the periphery of the testis, which is often smaller than the
nonnal testis (Fig. 134a). Varicocele is more common on the left side:
there may be associated infertility. The underlying testis must be
scanned to exclude a tumour and varicocele must be differentiated from
spennatocele (Fig. 134b). A Val salva manoeuvre will often cause the
veins to dilate.
Fig. 134a. Transverse scan: a varicocele with multiple dilated veins.
Fig. 134b. Transverse scan: a spermatocele.
CHAPTER16
Gynaecology
(non-pregnant female pelvis)
Indications 196
Preparation 196
Endovaginal ultrasound 197
Normal anatomy 198
Abnormal uterus 210
Abnormal ovary 216
Pelvic inflammatory disease 219
Fluid in the pelvis (ascites) 219
Pelvic abscess 220
Fallopian tubes 220
Pelvic varices 221
Ectopic pregnancy 222
196 Gynaecology (non-pregnant female pelvis)
Indications
1. Pelvic pain. including dysmenorrhoea (painful menstruation).
2. Pelvic mass.
3. Abnormal vaginal bleeding.
4. Abnormal vaginal discharge.
5. Amenorrhoea (missed or absent menstrual cycle).
6. To confirm the presence and check the position of an intrauterine
contraceptive device.
7. Infertility: hysterosalpingography may also be needed.
8. Genital tract developmental abnormality: hysterosalpingography
may also be needed.
9. Urinary or bladder symptoms (see also Chapter 14).
10. Diffuse abdominal pain.
11. Follicular monitoring in investigation of infertility.
Ultrasound does not demonstrate the anatomy
of vesico-vaginal fistula. It may help to exclude
complications.
Preparation
1. Preparation of the patient. The bladder must be full. Give 4 or 5
to micturate). Alternatively. fill the bladder through a urethral
of infection.
2. Position of the patient. The patient is
usually scanned while lying comfortably on
her back (supine). It may be necessary to
rotate the patient after the preliminary scans.
Erect scanning is occasionally needed.
Apply coupling agent liberally to the lower
abdomen: it is not usually necessary to
cover the pubic hair. but. if required. apply
freely.
4. Setting the correct gain. Position the
transducer longitudinally over the full
bladder and adjust the gain to produce the
best image.
3.S MHz
adults
SMHz
children
1 litre total
adjust
gain
y
Gynaecology (non-pregnant female pelvis) -197
Scanning technique
Start with longitudinal scans, first in the midline
between the umbilicus and the pubic symphysis.
Then, repeat more laterally, first on the left side
and then on the right. Angle the transducer from
side to side and longitudinally to identify the
uterus.
Next, scan transversely. Start just above the
pubic symphysis and move upwards to the
umbilicus. Transverse scans are important over
the lower pelvis but are less effective above the
level of the uterus.
If necessary, turn the patient obliquely (30-40)
to identify the ovaries. Scan each ovary obliquely,
from the contralateral side of the abdomen (see
also pp. 204-209).
Endovaginal ultrasound
to identify ovaries
A different and specific transducer with a long handle is needed to
perfonn ultrasound from the vagina: specialized training is necessary.
Put sufficient coupling agent inside a condom or other disposable plastic
cover to provide good contact: the cover also prevents infection. Do not
use any other trWlSducer or any Wlcovered trWlSducer.
Endovaginal
transducer
Endovaginal transducer with
cover and coupling agent
With this technique, the bladder must be empty.
The field of view by endovaginal sonography is much smaller and
considerable experience is needed both to obtain satisfactory images
and to interpret them. The technique is very useful for imaging an early
pregnancY] and some uterine, fallopian tube or ovarian masses (including
ectopic prgnancy).
Endovaginal sonography can be misleading if
the operator is not well trained.
anterior
abdominal wall
.... .
: ' - : ~ ~ ~ ~ f : ~ : : ~ :
right
ovary
left
ovary
Normal anatomy
Locate the vagina and the uterus on a longitudinal scan.The vagina is
close to the postero-inferior wall of the urinary bladder and the walls of
the vagina will appear as hypoechogenic structures surrounding the
more echo genic vaginal mucosa (Fig. 135a). Follow the vagina superiorly
and the tissues will expand into the pear-shaped uterus, superior to the
vagina but with different echogenicity (varying with the phase of the
menstrual cycle) (see p. 212). Adjustment of the gain may be necessary
during these initial scans to obtain the best image.
The uterus has two different zones of echogenicity. The muscles in the
uterine wall are hypoechogenic, but the pattern of the endometrium
varies (Fig. 135b). In the first half of the menstrual cycle (post-
menstruation) the endometrium is thin ~ d hypoechogenic. In the
second half, the premenstrual phase, the endometrium is hyperechogenic
(see also Fig. 148, p. 212).
The uterus may not be exactly in the long axis of the pelvis and may be
seen tangentially. The long axis of the uterus is measured from fundus
to cervix.
The normal postpubertal nulliparous uterus measures 4.5-9.0 cm in
length, 1.5-3 cm antero-posteriorly, and 4.5-5.5 cm in the transverse
diameter. Uterine dimensions increase by 1.0-1.2 cm with parity, and
the body of the uterus becomes more rounded (Fig. 140, p. 202). The
antero-posterior diameter of the uterine cervix should not exceed the
antero-posterior diameter of the uterine body (for measurements in
children, see p. 199).
uterus
Full bladder
*'
R
<r .% ..
->(.' .--
length
4.5-9.0 em
AP diameter
1.5-3.0 em
vagina
Adult anatomy
transverse diameter
4.5-5.5 em
Full bladder
Gynaecology (non-pregnant female pelvis) 199
Fig. 135a. Longitudinal (left) and transverse (right) scans of a normal vagina (arrows).
Fig. 135b. Longitudinal scan of a normal uterus.
Fig. 135c. Transverse scan of a normal uterus.
The pre-pubertal uterus
As the child grows, the ratio ofthe uterine cervix
to the uterine body changes. In childhood the
body of the uterus is smaller than the cervix, but
with increasing age, the uterine body grows
larger and the endometrium is not demonstrated.
Full bladder
....

1-12 years
length uterus
2-3.3 em
AP di ameter
0.5-1 em
Vagina, rectum and bladder
Transverse scans should start with steep angulation posteriorly and
downwards. IdentifY the vagina, the rectum and the lower part of the
urinary bladder. Examine the shape of the bladder at this level. Keeping
the transducer in the midline, slowly sweep the scan plane from the
bottom to the top of the pelvic cavity (Fig. 135, p. 199).
IdentifY the junction of the vagina with the cervix of the uterus, then the
ligament on either side of the cervix, the narrow "neck" (isthmus) and the
body of the uterus. Look for both ovaries (see pp. 204-208).
The normal echo pattern of the vagina may be
altered by a tampon (Fig. 136a, b) or foreign
objects, such as a pessary (Fig. 136c).
Fig. 136a. Longitudinal scan: a tampon in the vagina. (The uterus is retroverted; see p. 203).
Fig. 136b. Transverse scan of the same patient.
Fig. 136c. Transverse scan: a pessary in the posterior vaginal fornix with an acoustic shadow
below it.
~
..
~ ............
-< ..............
-(..... . ... )-
.r.. ... y ..
Intrauterine contraceptive device
An intrauterine contraceptive device (IUD) will appear as a linear or
interrupted hyperechogenic line within the endometrial cavity or cervical
canal and may produce distal acoustic shadowing (Fig. 137) (see also
p.229).
Fluid in the posterior cul-de-sac
It is not unusual to fmd a small amount of fluid in the posterior cul-de-
sac following ovulation or menstruation (Fig. 138). An echo-free cross-
sectional diameter of less than 1 cm is normal.
Fig. 137a. Longitudinal (left)
and transverse (right) scans:
an intrauterine contraceptive
device causing acoustic
shadows.
Fig. 137b. Longitudinal scan:
an IUD in the cervical canal,
extending into the vagina.
Fig. 138a. Longitudinal
section showing a small
amount of fluid in the cul-de-
sac; this is normal after
ovulation or menstruation.
Fig. 138b. Transverse scan
of the same patient.
Uterine cervix
Scan the uterine cervix in different projections
and note any abnormal variation in size or
shape (Fig. 139a). After pregnancy the cervix
may be asymmetrical (Fig. 139b).
Fig. 139a. Longitudinal scan: the normal uterine cervix.
Fig. 139b. Longitudinal scan: a multiparous cervix.
Following each pregnancy, the uterus increases in size and the body of
the uterus becomes more rounded. Thus, the uterus of a multiparous
patient (Fig. 140) will look quite different from that of a nulliparous
patient. Record the uterine dimensions. (See also pp. 198, 199.)
Fig. 140. Longitudinal scan: a bulky multiparous uterus.
The postmenopausal pelvis
1. Uterus. After the menopause the uterus is much smaller and will
appear homogeneous: the endometrial cavity will not be visible.
2. Ovaries after the menopause. The ovaries are small and often very
difficult or impossible to recognize with ultrasound. If seen, they are
hyperechogenic, wi thou t any follicles and similar to the surrounding
tissues.
Position of the uterus
The uterus may rotate so that the fundus of the uterus may be behind
the cervix (retroversion). It may also rotate forward (anteversion).
If the body of the uterus bends forward at the cervix. it is anteflexed
(Fig. 141a). When the uterus bends backwards at the cervix. it is retro-
flexed (Fig. 141b).
Fig. 141 a. Longitudinal scan: an anteflexed uterus. which bends forward at the cervix and lifts
the posterior bladder wall.
Fig. 141 b. Longitudinal scan: a retroflexed uterus.
If the uterus is not identified. check the patient's surgical history to
exclude a hysterectomy. When there has been pelvic surgery, look
carefully for the remnants of the cervix, suggesting a partial hysterectomy
(Fig. 141c) (see also p. 207 for useful scanning techniques).
Fig. 141 c. Longitudinal scan: only the uterine cervix is seen; the body of the uterus has been
surgically removed (partial hysterectomy).
When normal pelvic anatomy is not clearly recognized, give
the patient more fluid to fill the bladder (see pp. 206-207).
Ovaries
Scan the tissues on the left close to the uterus.
Angle the transducer as required to locate the
left ovary, which will appear as an ovoid (egg-
shaped) structure, less homogeneous than the
uterus but with the same or slightly less
echogenicity: there will often be distal acoustic
shadowing (Fig. 142a).
Fig. 142a. Longitudinal scan: normal left ovary.
1tf:-t
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Y
Y
The ovaries can vary in position but always lie behind the bladder and
the uterus. They are most commonly found in the adnexal space
laterally (Fig. 142b).
Fig. 142b. Angled transverse scan: normal right ovary.
An ovary may be located in the cul-de-sac or cephalad to the fundus of
the uterus (Fig. 142c). In postmenopausal women, the ovaries are small
and may be difficult to identify.
Fig. 142c. Transverse scan: a small ovary lying unusually high in the pelvis.
If it is difficult to differentiate between the uterus and the ovaries, move
the uterus manually per vagina and continue to scan, using different
projections and positions to clarify the anatomy. The same technique
can be used when there is a lower pelvic mass (see also p. 207).
When the ovaries cannot be identified, the following techniques may be
helpful:
1. Tum the patient obliquely and scan the opposite ovary through the
full bladder (Fig. 142d).
Fig. 142d. Oblique scan: the ovary is seen through the bladder.
2. Reduce the gain settings. If the gain is set too high, the ovary may
blend into the surrounding parametrium and be difficult to identify
(Fig. 142e. O.
Fig. 142e. Gain settings too high. resulting in reverberation and artefacts in the bladder and
poor definition of the uterus.
Fig. 142f. Gain setting too low, so that the posterior portion of the uterus is not clearly seen.
If the ovaries are still difficult to identify, there may be too much or too
little urine in the bladder. If the bladder does not extend to the level of
the uterine fundus, it is probably not full enough and the patient sbould
drink more water (Fig. 143). Rescan 30 minutes later: if the bladder is
then full enough, try to identify the ovaries.
Fig. 143a. Inadequate filling of the bladder, which does not cover the uterus, making it difficult
to see.
Fig. 143b. The bladder of the same patient is now properly filled and extends past the fundus of
the retroverted uterus.
If the bladder is overfilled, it will push the ovaries against the uterus or
laterally onto the psoas muscle. Ask the patient to partially empty the
bladder (give her a specific measure, such as a small jug or bowl to fill).
Then repeat the scan.
Even when the bladder is correctly filled, the ovaries may be difficult to
image because of overlying bowel gas. This is particularly important if
the ovary lies higher in the pelvis than usual (Fig. 143c).
Fig. 143c. Transverse scan: an ovary lying unusually high in the pelvis.

U
If necessary, scan the patient in the erect and oblique-erect positions.
This may displace the gas-filled loops of bowel and allow the ovaries to
be seen more clearly.
30-40
If the normal pelvic anatomy cannot be demonstrated, gently insert
20 ml of water at body temperature into the vagina while scanning above
the pubic symphysis. The fluid will surround the cervix and simplifY
recognition. This procedure is particularly helpful in differentiating
between partial and total hysterectomy when not possible by clinical
examination.
If it is difficult to locate a retrouterine mass, insert 200 ml of warm water
into the rectum while continuing to image the area. Microbubbles in the
water will appear as strongly reflective echoes which will delineate the
anterior wall of the rectum, and allow recognition of intraluminal
masses, such as faeces, which are a common source of error.
Normal ovaries
When the ovaries have been found, check for
displacement of any surrounding structure.
Check the normal echo pattern and look for any
distal acoustic enhancement. If there are
anechoic spaces within or on the surface of the
ovary, these are probably ovarian follicles (see
p. 209). Reduce the gain when scanning the
ovary because normal ovarian tissue transmits
the echoes and enhances the deep tissues.
Measure the size of each ovary (Fig. 144).
Examine the tissue around the ovary for cystic.
solid or fluid-filled masses. Look particularly for
fluid in the cul-de-sac. Examine both ovaries.
An ovary should not normally be found in front
of the uterus. If it is in an abnormal position,
rotate the patient to see if it is fIXed by adhesions
and note whether it is significantly enlarged.
As already noted, the gain setting must be
varied while scanning the pelvis to obtain the
best images (Fig. 142e, f. p. 205). The relation-
ship of the pelvic organs may be more easily
seen by slow. continuous scans. taking about
10 seconds.
Fig. 144a. Longitudinal scan: a normal right ovary.
Fig. 144b. Transverse scan: a normal right ovary.

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adjust the gain
Osee 10 sec
I
v
slow scanning
Ovarian follicles
Follicles nonnally show as cyst -like anechogenic spaces within or
around the surface of the ovary and are best seen when the gain is low.
Depending upon the phase of the menstrual cycle. the cyst may be up
to 2.5 cm in diameter. Simple cysts measuring less than 5 cm may be
physiological and will change. become smaller or disappear (Fig. 145).
If there is concern that a cyst is neoplastic. the patient should be
scanned both early and late in the menstrual cycle. Follicular cysts
should regress and nonfunctional cysts should not change in size. Scan
after another month if still in doubt (see also p. 216).
Fig. 145a. Longitudinal scan: two follicular cysts within the ovary.
Fig. 145b. Longitudinal scan: an ovary with several surface follicular cysts.
Abnormal uterus
Myomas (fibroids)
Myomas appear in various ways on ultrasound examination. Most will
be seen as multiple, well defined, homogeneous, hypoechogenic, nodular
masses, either subserosal, submucosal or interstitial. Older myomas
become hyperechogenic and some will develop a complex echo pattern
as a result of central necrosis. There may be bright echoes from
calcification. Rapidly growing myomas, as may occur in pregnancy, may
simulate hypoechogenic cysts. Multiple projections are needed to
differentiate between myomas and tubo-ovarian masses. Some myomas
are pedunculated. Uterine myomas can indent the posterior wall of the
bladder (Fig. 146).
Fig. 146a. Longitudinal scan: a uterine myoma elevating the posterior wall of the bladder.
Fig. 146b. Transverse scan: a uterus enlarged by multiple myomas, which distort the bladder.
Fig. 146c. Longitudinal scan: a myoma with a central cystic area, the result of extensive
necrosis.
Fig. 146d. Pedunculated myoma shown as an irregular complex mass, lying between the ovary
and the uterus.
Myomas may also contain calcium, which can present as hyperechogenic
structures with distal shadowing (Fig. 146e). Myomas are almost always
multiple (Fig. 146b) and frequently distort the normal contours and the
endometrial canal of the uterus.
Fig. 146e. Longitudinal (left) and transverse (right) scans: a uterine myoma with peripheral
calcification.
Myomas can also originate in the cervical part of the uterus and may
cause distortion or blockage of the cervical canal (Fig. 1460.
Fig. 146f. Longitudinal scan: a myoma distorting the posterior part of the uterine cervix.
Developmental variants
A bicornuate uterus may be identified by the presence of two endometrial
canals or two uterine fundi on transverse scans (Fig. 14 7). Care must be
taken not to confuse a bicornuate uterus with an adnexal mass. A
double uterus has two endometrial canals and two cervices: if there is
an adnexal or other mass, there will be only one canal.
The endometrium (lining of the uterus)
The normal pattern varies with the stage of the menstrual cycle. In the
secretory phase (at the beginning of the cycle) the endometrium appears
thin and hypoechogenic. In the proliferative phase (mid-cycle) the
central part of the endometrium becomes hyperechogenic and is
surrounded by a hypoechogenic rim. During the menstrual phase the
endometrial cavity becomes totally hyperechogenic and thickened
owing to sloughing endometrial tissue and blood clots (Fig. 148) (see also
pp. 198 and 199).
Fig. 147a. Transverse scan:
a bicornuate uterus.
a bicornuate uterus; there are
two distinct endometrial
canals.
the uterine endometrium at
the proliferative mid-cycle
phase.
Fig. 148b. Transverse scan
of the same patient at the
same phase in the cycle.
In women with an imperforate hymen, or in those who have undergone
ritual circumcision, blood may accumulate in the endometrial canal
(haematometrium) or in the vagina (haematocolpos) and will be
hypoechogenic compared with the endometrium (Fig. 149).
Fig. 149a. Haematometrium and haematocolpos: the uterus and vagina are filled with fluid
because the hymen is imperforate.
Fig. 149b. Haematometrium and haematocolpos: the uterine cavity and the vagina are filled
with fluid.
The endometrial canal may be filled with pus from infection (pyometria).
This will appear hypoechogenic with internal echoes (Fig. 149c). Fluid
resulting from infection may also collect in the fallopian tubes
(hydrosalpinx) and may spread to the cul-de-sac (Fig. 150) (see also
p.220).
Fig. 149c. Transverse scan: fluid within the endometrial cavity.
Fig. 150. Transverse scan: hydrosalpinx.
Malignant disease
A poorly defined mass within the uterus may be malignant and is
usually an endometrial carcinoma. The endometrium becomes
hyperplastic and the hypoechogenic tumour may spread into the
myometrium. When the tumour is advanced, there may be necrosis,
resulting in a complex ultrasound pattern: there may be distension of
the endometrial cavity of the uterus (Fig. 151).
Fig. 151a. Longitudinal midline scan: a large endometrial carcinoma distends the cavity of the
uterus and is invading the posterior myometrium.
Fig. 151 b. Longitudinal scan: an extensive endometrial carcinoma enlarging and distorting the
uterus.
Fig. 151 c. Longitudinal scan: an extensive choriocarcinoma, which was detected 14 months
after a normal pregnancy and now distorts the uterus.
Early carcinoma of the cervix is very difficult to recognize with ultrasound.
Any ill-defined mass in the cervix is likely to be malignant (most myomas
are well defined and the bright echoes of calcification may be seen). If the
tumour is large, the echo pattern will be complex and very varied
(Fig. 152). The tumour may infiltrate the surrounding tissues, and the
bladder, vagina and rectum should be carefully scanned (see p. 207 for
the use of fluid to obtain better definition).
Fig. 152. Longitudinal scan: a large carcinoma of the cervix uteri.
Uterine endometriosis
Hypoechogenic spaces in the myometrium near the endometrium may
represent adenomyosis (uterine endometriosis). The spaces will be more
prominent during and immediately after menstruation. Small retention
cysts (follicles) in the uterine cervix, close to the canal, should not be
mistaken for endometriosis. A pelvic mass may be an endometrioma
(Fig. 153) (see also Fig. 159, p. 219) or ectopic pregnancy (p. 222).
Fig. 153. Transverse scan: endometrioma.
Remember: always vary the gain setting
throughout pelvic ultrasound examinations to
obtain the best images.
Abnormal ovary
The normal ovary is slightly less echogenic than the uterus and less
homogeneous because of the presence of small follicles (Fig. 154) (see
also pp. 208-209). Identification in postmenopausal women can be
difficult, particularly after the age of 50 (see pp. 204-207).
Fig. 154. Longitudinal scan: a normal ovary.
Ovarian cysts
A follicle is a physiological ovarian cyst which normally disappears
during the second half of the menstrual cycle (see p. 209). If the follicle
fails to rupture in mid-cycle, it will become a follicular cyst, which is one
cause of ovarian cysts; these may be over 3 cm in diameter. Immediately
after rupture there may be a little fluid in the cul-de-sac (Fig. 138,
p.201).
A simple cyst has smooth walls, no internal echoes, good distal wall
enhancement and is almost always benign (Fig. 155a). Vestigial embryonic
structures in the pelvis can give rise to simple cysts.
Fig. 155a. Transverse scan: an ovarian cyst with smooth walls.
, On ultrasound, ovarian ,:,.cYsts can appear cystic or
almost solid or with internal, echoes from
haemorrhage, nodules or septations. Complex cysts
have strong back waiF enhancement '. an.d variable
internal patterns and ate more likely to be malignant. ' .
------
Small or medium-sized ovarian cysts lying behind the uterus or bladder
cannot be seen easily. particularly if the bladder is only partly filled.
Large ovarian cysts often lie above the uterine fundus when the bladder
is full. and may cause distortion of the bladder by external pressure
(Fig. 155b). A very large cystic mass may be mistaken for the urinary
bladder: both should be identified (Fig. 155c) (see also pp. 204-207 for
useful scanning techniques).
Fig. 155b. Longitudinal scan: a septate ovarian cyst distorting the bladder.
Fig. 155c. Longitudinal scan: an ovarian cyst which is so large that it may be mistaken for the
urinary bladder.
Fig. 155d. A multiseptate ovarian cyst.
Dennoid cysts (cystic teratomas) appear as solid or complex masses
with areas of acoustic shadowing due to calcification in bone or teeth.
If there is any doubt. X-ray the pelvis (Fig. 156).
Fig. 156. A dermoid cyst with internal bone. which is causing acoustic shadowing.
Pelvic echinococca/ (hydatid) cysts
Hydatid cysts are of different sizes, often multiple and in almost any
position; some have internal septa (Fig. 157). If echinococcosis is
suspected, scan the liver and X-ray the chest for other cysts.
Fig. 157a. Transverse scan: an echinococcal (hydatid) cyst with internal septa.
Fig. 157b. An enlarged view of the same hydatid cyst from a different angle; there is separation
of the endocyst (the germinal membrane) from the external cyst wall.
Solid ovarian masses
Solid masses are rare and have often undergone necrosis or internal
haemorrhage by the time they can be recognized ultrasonically. Solid
ovarian masses may be confused with pedunculated fibroids and a
careful search for a uterine connection should be made (Fig. 158).
Fig. 158. Transverse scan: a large, solid, non-homogeneous ovarian mass elevating the
posterior wall of the bladder.
Cystic masses in the pelvis of postmenopausal women
are probably malignant.
----------------- - ---
Pelvic inflammatory disease
In pelvic inflammatory disease, there may be adhesions, distortion of
the tissues, displacement of the uterus or ovaries, fIxation, and changes
in the echogenicity ofthe parametrial tissues. However, ultrasound may
be normal and clinical examination may be more accurate. Pelvic
tuberculosis cannot be distinguished from other inflammatory processes.
A mass may be an endometrioma (Fig. 159), abscess or ectopic preg-
nancy; exact localization may be difficult less (see also pp.220 and 222).
Fig. 159. Transverse scan: bilateral, predominantly cystic, endometriomas.
Fluid in the pelvis (ascites)
If there is excess fluid, suspect ascites, blood, pus or the contents of a
ruptured cyst. Multiple projections will help assessment (Fig. 160).
The fluid may be echo-free or produce internal echoes as a result of
debris. Fluid collections may also be found in the vagina and in the
endometrial canal (p. 213) (see p. 201 for normal pelvic fluid).
Fig. 160a. Longitudinal scan: the uterus appears to be floating in peritoneal fluid (ascites).
Fig. 160b. Transverse scan: the same patient. The ovaries also seem to be floating.
r ,
many. causes of pelvic masses. Ultrasound cannot
' .. ,.. .
dlstmgulsh between them.
Pelvic abscess
Any localized, complex pelvic mass may be inflammatory, but pyogenic
and tuberculous infections look the same. It is often impossible to be
sure of the exact location or etiology of an inflammatory mass: clinical
examination is very important (Fig. 161).
Fig. 161 a. Transverse scan: a pelvic abscess shown as an irregular complex mass.
Fig. 161 b. Longitudinal scan: the same pelvic abscess lying partly behind the uterus.
Fallopian tubes
It is not easy to demonstrate a normal fallopian tube with ultrasound.
The fallopian tubes vary in both size and position, and it is difficult to
be sure that there is an abnormality unless there is a significant local
change, for example, partial enlargement of one tube. If the tubes are
fluid-filled, it may be difficult to differentiate bowel, but bowel shows
peristalsis whereas the fallopian tubes will not alter significantly over a
period of a few hours. Tubal obstruction cannot be recognized with
ultrasound unless there is tubal swelling above it.
Enlargement of part of one fallopian tube may be due to an ectopic
pregnancy (see p. 222) which will cause a tubular, fluid-filled, echo-free
(or mixed) mass near to the uterus. However, any pyosalpinx (tuberculous
or pyogenic) will appear very similar. Clinical signs are the only way to
differentiate a hydrosalpinx from a pyosalpinx (Fig. 162).
Fig. 162. Longitudinal scan: a large tubo-ovarian mass, close to the uterus.
Pelvic varices
Dilated pelvic veins can be painful, particularly in the premenstrual
phase. Ultrasound will demonstrate multiple echo-free, tubular struc-
tures around the uterus and occasionally between the uterus and the
bladder. There may be only a single dilated vein, which may be mistaken
for a hydrosalpinx. Differentiation can be made by examining the patient
tilted head downwards. A dilated vein will empty in this position,
whereas a hydrosalpinx will not change (Fig. 163).
Fig. 163. Longitudinal scan of a patient with pelvic varices.
Ectopic pregnancy
A pelvic mass in a woman of childbearing age may be an ectopic
pregnancy. Although ultrasound may be useful, it is not an entirely
reliable method of diagnosing ectopic pregnancy. It is sometimes
possible to demonstrate the ectopic sac and an embryo (see p. 230), but
more commonly there is pooled blood in the pelvic cul-de-sac and an
enlarged fluid-filled fallopian tube (Fig. 164) (see also p. 220).
Fig. 164a. Transverse scan of an ectopic pregnancy, showing a small embryo. Movement of
the embryo's heart could be seen.
Fig. 164b. Transverse scan: ectopic pregnancy causing a decidual reaction in the uterus due to
endocrine stimulation. The pregnancy lies in the left adnexa.
CHAPTER 17
Obstetrics
Introduction 224
Preparation 227
Early pregnancy 227
Intrauterine contraceptive device 229
Ectopic pregnancy 230
The embryo 230
The yolk sac 231
Multiple pregnancy 231
Abnormalities in the first three months of pregnancy 232
Estimation of fetal size and age (fetal biometry) 236
Recognition of intrauterine growth retardation 241
Quality control 244
Scanning a patient for another physician 244
Normal pregnancy 245
The abnormal fetus 261
Amniotic fluid 270
The placenta 272
The incompetent cervix 278
The umbilical cord and vessels 279
Multiple pregnancy 279
Summary: scanning during pregnancy 280
224 Obstetrics
Introduction
Diagnostic ultrasound has been used in obstetrics for nearly 30 years.
Although generally considered safe, there is continuing study and
research to confirm this. It is a very important technique for examining
pregnant women and can be used when clinically indicated at any time
during pregnancy.
Is ultrasound safe during pregnancy?
Yes, as far as is known. However, it should be used only when there is
a good clinical reason.
Is a clinically normal pregnancy a good reason for using
ultrasound?
This is controversial and is still being investigated. However, there is
agreement that there are two stages during a normal pregnancy when
ultrasound scans will be the most useful and provide the most information.
These stages are:
1. At 18-22 weeks after the first day of the woman's last menstrual
period
2. At 32-36 weeks after the first day of the woman's last menstrual
period
Most informative times for a first scan
1 2 3 4 5 6 7 8
9 10 11 12 13 14 15 16
17 23 24
weeks
Most informative times for a second scan
25 26 27 28 29 30 31
ElEDIIED.
37 38
39 40
weeks
When is ultrasound not recommended?
There is no indication for an ultrasound examination in the first
trimester of pregnancy unless there is a clinical abnormality (see p. 226).
Why is a scan not recommended at the mother's first visit?
Some physicians do recommend an ultrasound examination at the
time of the mother's first visit, but there is no reason to do this provided
the clinical examination is normal. When considered necessary, scanning
during weeks 18-22 of pregnancy will provide much more important
information.
Why consider scanning during a normal pregnancy?
Many physicians consider that scanning is unnecessary during a
clinically normal pregnancy. Others recommend scanning because
many obstetric abnormalities cannot be detected by clinical examination.
1. 90% of developmental fetal abnormalities occur without any family
history and very few of the mothers show any obvious risk factors.
2. There can be significant fetal abnormalities even in a clinically
normal pregnancy.
3. Neither clinical examination nor a family history is an entirely
r e l i b ~ e way to detect multiple pregnancy.
4. A sigrlificant number of mothers with a low-lying placenta (placenta
praevla) show no evidence until bleeding starts at the onset of
labour. The situation can then be extremely dangerous. especially
if the patient is a long way from the nearest hospital.
5. Up to 50% of mothers who claim to know their obstetric dates with
certainty are in fact more than two weeks in error when gestational
age is calculated with ultrasound. A discrepancy of two weeks can
be critical for the survival of an infant who has to be delivered early
because of some antenatal complication.
What are the objections to scanning during a normal
pregnancy?
Many physicians believe that the possible risks and the costs of
scanning every clinically normal pregnancy are not justified by the
benefits for the patient.
This decision. to scan or not to scan a normal pregnancy. must be made
by the physician and each patient. There are no universally accepted
guidelines at present.
Obstetrics 225
226 Obstetrics
What is important in the 18-22 week scan?
This is the best time during pregnancy to:
1. establish the gestational age accurately;
2. diagnose multiple pregnancy;
3. diagnose fetal abnormalities;
4. locate the placenta and identify patients in whom there is a risk of
placenta praevia;
5. recognize myomas or any other unexpected pelvic mass that may
interfere with pregnancy or delivery.
What is important in the 32-36 week scan?
This is the best time during pregnancy to:
1. recognize intrauterine growth retardation;
2. recognize fetal anomalies that were not detected at the first scan;
3. confirm the presentation and position of the fetus;
4. locate the placenta accurately;
5. assess the amount of amniotic fluid;
6. exclude possible complications, e.g. myoma, ovarian tumour.
What are the indications for a scan before 18 weeks?
The patient should have a careful clinical examination as soon as there
is either a positive pregnancy test or a missed menstrual period. An
ultrasound scan is helpful when there is clinical evidence that the
pregnancy may not be normal or if there is any doubt about the
gestational age.
What can be learned from an early scan (before 18 weeks)?
Ultrasound in the early weeks of pregnancy can:
1. confirm the pregnancy;
2. accurately estimate gestational age;
3. locate the pregnancy (intra- or extrauterine);
4. recognize single or multiple pregnancy;
5. exclude molar pregnancy;
6. exclude pseudo-pregnancy due to a pelvic mass or hormone-secreting
ovarian tumour;
7. diagnose myomas or ovarian masses which might interfere with
normal delivery.
Preparation
1. Preparation of the patient. The bladder must be full. Give 4 or 5
to micturate). Alternatively. fill the bladder through a urethral
of infection.
usually scanned while lying comfortably on
her back (supine). It may be necessary to
rotate the patient after the preliminary scans.
Apply coupling agent liberally to the lower
abdomen: it is not usually necessary to
cover the pubic hair but. if required. apply
freely;
Obstetrics 227
1 litre total
transducer. Use a 5 MHz transducer for
3.5 MHz 5 MHz
thin women.
4. Setting the correct gain. Position the
transducer longitudinally over the full
bladder and adjust the gain to produce the
best image.
Early pregnancy
adjust
gain
v
Location of the gestational sac is the first evidence of pregnancy. It can
often be recognized in the uterus after five weeks of amenorrhoea. and
may be located asymmetrically (Fig. 165).
Fig. 165. The gestational sac at 5-6 weeks. The centre is hypoechogenic. surrounded by a
double echogenic ring. The inner ring is complete and is the gestational sac. The outer ring is
incomplete and is the lining of the uterus. These two rings are separated by the anechogenic
space of the residual endometrial (uterine) cavity.
228 Obstetrics
All normal pregnancies should be recognizable after 6 weeks as a well
defined "double echogenic ring" in the uterus. The inner ring is of
uniform echogenicity and is 2 mm or more thick. Around it is a thin
echogenic ring, which does not encircle the entire gestational sac.
Between the two rings is the anechogenic residual uterine cavity
(Fig. 165, p. 227).
At 5-6 weeks, the greatest diameter of the gestational sac is approx-
imately 1-2 cm. At 8 weeks the sac should occupy half the uterus; at
9 weeks it should take up two-thirds of the uterus, and at 10 weeks it
should fill the uterus.
The gestational age can be estimated to within one week from the mean
dimension ofthe sac. Using a longitudinal scan, measure the maximum
dimensions of the sac in the long axis (length), and at 90 to this in the
antero-posterior (AP) dimension (Fig. 166, upper scan). Make a transverse
scan at right angles to the longitudinal scan plane and measure the
greatest width of the sac (Fig. 166, lower scan). The mean dimension
of the sac is the sum of these three measurements divided by 3.
Mean gestational sac dimension = Length + AP + Width
3
The gestational age of the fetus can be estimated by reference to local
standard development tables (see also p. 236).
Five or six weeks is the earliest stage at which a pregnancy
can be recognized with ultrasound.
Fig. 166. Measurement of the gestational sac. The length is the longest internal dimension in
the longitudinal plane (upper). The antero-posterior measurement is the widest part of the sac
at right angles to the length (upper). The width is the widest part in a transverse scan (lower).
Intrauterine contraceptive device (IUD)
Is the IUD there?
Ultrasound is an ideal way to determine whether an intrauterine con-
traceptive device is in the uterus in its correct position, or whether it has
moved outside the uterus (see also p. 201).
If the patient believes that there is an intrauterine device but it cannot
be imaged within the uterus or pelvis, the whole abdomen should be
scanned. IUDs can migrate as far as the splenic area. If there is still any
doubt, a plain X-ray of the abdomen should be taken (provided pregnancy
has been excluded), making sure that it includes the whole abdomen
from the diaphragm to the bottom of the pelvis.
IUD and normal pregnancy
If the IUD is located well away from the implantation site of the embryo,
pregnancy can be allowed to progress without interference (Fig. 167).
If the IUD is partially expelled, the pregnancy can be allowed to progress
without interference.
If the IUD strings can be seen in the vagina, the device can be carefully
removed.
In all other cases, spontaneous abortion is likely to occur and the
patient should be warned of this possibility.
Fig. 167. Pregnancy in spite of an IUD. There are bright multiple echoes from an intrauterine
loop next to the gestational sac.
Obstetrics 229
230 Obstetrics
Ectopic pregnancy
If there is an ectopic pregnancy, a gestational sac may be seen outside
the uterus. Sometimes there is a sac-like structure in the uterus despite
the pregnancy being ectopic (Fig. 168). The real sac can be distinguished
from the "pseudosac" by the presence of fetal parts, a yolk sac within the
real sac or by a single ring around the pseudosac instead of a double ring
(see p. 228) (see also p. 222).
Fig. 168. An embryo within an extrauterine mass. There is a well-defined sac in the uterus,
containing fluid only.
The embryo
Although the gestational sac can be recognized at 5 weeks in some
patients and at 6 weeks in the majority, the embryo does not become
visible until the eighth gestational week (Fig. 169a). It will then be shown
as a focal area of echoes, often lying eccentrically within the gestational
sac. If the fetus is alive, the heart will be recognized lying in mid-embryo,
usually seeming to lie anterior to the rest of the thorax.
Fig. 169a. A normal9-week pregnancy, with thick, echogenic decidual reaction around the sac.
Mter the ninth or tenth week, the fetal head can be distinguished from
the body and movements can be seen. At 10 weeks the fetus becomes
more human in appearance (Fig. 169b). Mter the twelfth week, the skull
becomes visible.
Fig. 169b. A normal 12-week pregnancy. The crown-rump length (CRL) and biparietal diameter
(BPD) are shown (see pp. 236-237).
The yolk sac
From about 7 weeks onwards. it is usually possible to see a round cystic
structure about 4-5 mm in diameter adjacent to the fetus. This is the
yolk sac. the site of the earliest blood cell formation. It disappears at
abou t the eleventh week. The yolk sac may not be seen in all pregnancies.
even when quite normal.
It is important to recognize that this cystic shadow is the yolk sac and
not mistake it for a second. twin embryo (Fig. 170). (The yolk sac is not
included in crown-rump measurements.)
Fig. 170. A normal yolk sac with a surrounding echogenic decidual reaction.
Multiple pregnancy
The earliest it is possible to diagnose multiple pregnancy is at about 8
weeks' gestation; however. not all gestational sacs go on to contain a
viable fetus. Never tell a patient that she has a multiple pregnancy until
more than one viable fetus is recognized and each is growing normally.
This is usually after about 14 weeks. and is best seen between 18 and 22
weeks (Fig. 171).
Fig. 171. Twin pregnancy: each embryo must be measured separately. usually requiring scans
at different angles.
Obstetrics 231
232 Obstetrics
Abnormalities in the first three months of pregnancy
Small gestational sac
A small gestational sac is usually due to a blighted ovum (anembryonic
gestation) and is a fairly common finding. On ultrasound examination
the gestational sac is found to be smaller than expected for the
gestational age. and the fetus cannot be demonstrated (Fig. 172).
Fig. 172. A blighted ovum. The sac is round. but the surrounding decidua is irregular and there
is no embryo.
If an early pregnancy is clinically normal, but an ultrasound scan shows
an enlarged uterus. an anembryonic gestation should be suspected:
repeat the examination after 7 days. Ifthe pregnancy is normal. the sac
should have grown. and the fetus and the heart activity should be clearly
seen at the second examination.
Fetal death (spontaneous abortion)
When there is a fetal or embryOniC death. the patient may remain
clinically normal and may continue to feel pregnant for days. There may
be a history of bleeding or abdominal cramp. The uterus may be normal,
small. or even enlarged if there is significant intrauterine haematoma.
The fetal pole may be visible but no heart action will be demonstrated.
If the examination is made during the first 8 weeks of pregnancy. it
should be repeated after another 7 days. After the eighth week. fetal life
should always be demonstrable in a normal pregnancy (Fig. 173).
Fig. 173. Fetal death. The sac is the correct size for the expected gestational age. but the
embryo is too small (and no heart beat was seen).
It should always be possible to demonstrate fetal
heart activity after the eighth week of pregnancy.
Empty uterus
The patient will have a history of amenorrhoea followed by loss of blood ,
sometimes with recognition ofthe fetus. Ifthis is recent, the uterus may
still be large, approximately the expected size for gestational age. The
scan will show the uterus to be empty.
Incomplete abortion
The patient may have a history of amenorrhoea, followed by loss of
blood; she may have seen the fetus. If this is recent, the uterus may still
be large, approximately the expected size for gestational age. However,
the uterus may be empty and the endometrial canal may be normal. If
the abortion is incomplete, the uterus will be smaller than expected for
gestational age and filled with an abnormally shaped sac (Fig. 174) or
with an amorphous mass of variable size, shape and echogenicity. This
is the retained placenta and blood clots (see also p. 235). There will be
no sign of fetal life.
Fig. 174. An incomplete abortion. The uterus is bulky, the sac is irregular and poorly echogenic.
There is no embryo.
It can be difficult to recognize the retained products of conception after
a spontaneous abortion. This diagnosis should not be made unless
there are identifiable parts, such as a yolk sac, gestational sac or dead
embryo. Endometrial thickening is not a reliable way of recognizing or
excluding retained products of conception, and a molar pregnancy must
be excluded (Fig. 175).
Fig. 175. Molar pregnancy. There is no sac, and the uterus is filled with echogenic material
without any retained products of conception.
Be warned: the patient's estimate of gestational age is
not always accurate.
Obstetrics 233
234 Obstetrics
Large uterus
The commonest causes of a uterus larger than expected are:
Hydatidiform mole.
Choriocarcinoma.
Intrauterine bleeding associated with spontaneous abortion.
Uterine myoma (fibroids).
1. Hydatidifonn mole. Clinical findings are nonspecific. Ultrasound
is almost always abnormal and shows a large uterus filled with a
mass of uniform echoes providing a regular speckled appearance:
the "snow-storm" effect. It may be difficult to distinguish a mole
from echo genic blood within the uterus. but blood is usually more
heterogeneous and less echogenic than a mole. which may have
cystic spaces (vesicles). In older patients in particular. a large
myoma may cause confusion. but moles will have stronger back wall
echoes and central necrosis (Fig. 176). It is important to remember
that the fetus may still be present and only part ofthe placenta may
be affected. Embryos in association with moles have a high incidence
of chromosomal abnormalities.
Fig. 176a. A hydatidiform mole filling the uterus with echogenic and cystic tissue.
Fig. 176b. A hydatidiform mole with a living embryo. There is an increased risk of chromosomal
abnormalities in the fetus and. as pregnancy progresses. there is an increasing likelihood of
fetal death.
2. Choriocarcinoma may be indistinguishable from a hydatidiform
mole by ultrasound. but it should be considered if the uterus is
much larger than expected and the ultrasound scan shows areas of
haemorrhage and necrosis rather than the uniform echoes of a
mole. The pattern of choriocarcinoma may be mixed. with both solid
and fluid echoes. rather than the homogeneous snow-storm effect
of a mole. Rarely there may be disease elsewhere: X-ray the chest to
exclude metastases.
3. Intrauterine haemorrhage due to threatened or spontaneous
abortion. This is mainly a clinical diagnosis based on bleeding in
early pregnancy: ultrasound may show a varying amount of blood
in the uterus, separating the chorioamniotic membrane from the
decidua (the lining of the membrane ofthe uterus), which shows as
a clearly defined anechogenic area. The blood may be completely
anechogenic or echogenic. It is usually heterogeneous (Fig. 177). It
is very important to search for signs of fetal life because this will
influence the way the patient is managed. If there is any doubt,
repeat scans at one- or two-week intervals to evaluate the progress
of the pregnancy.
Fig. 177. A poorly echogenic intrauterine haematoma, which is lifting the edge of the placenta
and distorting the gestational sac. This haematoma was absorbed and the embryo survived.
If there is any doubt after one scan, repeat in one
or two weeks.
4. Large irregular uterus. In the first trimester a large, irregular
uterus is usually due to uterine myomas (Fig. 178). Record the
size and pOSition of the myomas and estimate the potential difficul-
ties that they may cause during labour. The myomas should be
reviewed at 32-36 weeks' gestation. The central area may become
necrotic, showing a mixed or echo-free pattern. This does not
necessarily have any clinical significance. A myoma can be mimicked
by contraction of the uterine muscle, and the scan should be
repeated after 20-30 minutes to see if the contraction area changes.
Contractions are normal and indent the inner aspect of the uterus
(see p. 273).
Fig. 178. A myoma pressing on the gestational sac and also bulging outward from the uterus.
There is varying echogenicity in the myoma.
Obstetrics 235
236 Obstetrics
Estimation of fetal size and age (fetal biometry)
If gestational age and fetal development are to be estimated.
measurements must be obtained and then compared with local standard
values. Although there are many alternative measurements that can be
made. only a few are accurate and reliable.
Crown-rump length measurement (CRL)
The crown-rump length is the most reliable parameter for estimating
gestational age up to the eleventh week. After that. the curvature of the
fetus affects the reliability of the measurement. From the twelfth week
onwards. the biparietal diameter is more accurate.
There is excellent correlation between the crown-rump length and
gestational age from the seventh to the eleventh week of pregnancy:
biological variability is minimal and growth is not affected by pathological
disorders.
Using scans in different directions. the longest length of the embryo
should be found and a measurement made from the head (the cephalic
pole) to the outer edge of the rump (Fig. 179). The yolk sac should not
be included.
Fig. 179. Up to 11 weeks (left) measure the crown-rump length; after 11 weeks (right) measure
the biparietal diameter.
Using scans in different directions, measure the fetus
from. head to buttock. Measure the longest length,
ignoring any curvature. .
Do not include the fetal limbs or the yolk sac in this
measurement.
The gestational age can be determined from crown-
rump length to within approximately one week using
tables. Make sure that you use tables that
are appropriate for your patients and not derived from
some quite different population. .
Biparietal diameter
This is the most reliable method of estimating gestational age between
the 12th and the 26th weeks. After that. its accuracy may be lessened
by pathological disorders and biological variations that affect fetal
growth. It must be considered together with other measurements. such
as femoral length and abdominal circumference (Fig. 180).
The biparietal diameter (BPO) is the distance between the parietal
eminences on either side of the skull and is, therefore, the widest
diameter of the skull from side to side. Using scans at different angles,
the transverse section will be recognized when the shape of the fetal
skull is ovoid and the midline echo from the falx cerebri is interrupted
by the cavum septi pellucidi and the thalami (see pp. 247-248). When
this plane is found, the gain on the ultrasound unit should be reduced
and measurements made from the outer table of the proximal skull (the
part nearest to the transducer) to the inner table of the distal skull (the
part farthest away from the transducer). The soft tissues over the skull
are not included. This is the "leading-edge-to-leading-edge" technique.
Fig. 180. The fetal skull at 24 weeks' gestation, scanned at two different levels. The biparietal
diameter is the widest distance from the outer edge of the proximal skull to the inner edge of the
distal skull. At the correct level the midline falx is interrupted by the cavum septi pellucidi.
Obstetrics 237
238 Obstetrics
Fronto-occipital diameter
The fronto-occipital diameter is measured along the longest axis of the
skull at the level of the biparietal diameter (BPD), from outer edge to
outer edge.
Cephalic index
The BPD is a reliable estimate of gestational age except when the shape
of the head is abnormal or there is an abnormality of the intracranial
contents (Fig. 207. pp. 262-263). The adequacy of the head shape is
determined by comparing its short axis to its long axis-the cephalic
index.
Cephalic index =
Biparietal diameter x 100
Fronto-occipital diameter
Normal range ( 2 standard deviations) = 70-86
Head circumference
If the cephalic index is within the normal range. the BPD is acceptable
as an estimate of gestational age. If the cephalic index is outside this
range (less than 70 or greater than 86), the measured BPD should not
be used to determine the gestational age. Instead, the head circumference
can be used. On some ultrasound machines, this may be measured
directly. It can also be calculated (Fig. 181).
Head circumference =
(Biparietal diameter + Fronto-occipital diameter) x 1.57
Fig. 181. The two ways of measuring the head circumference.
Abdominal circumference
Abdominal circumference is used to detect intrauterine growth
disturbances. The measurement must be taken at the level of the fetal
liver. which is very sensitive to deficient nutrition (Fig. 182a). If the
measurement is less than normal there has probably been intrauterine
growth retardation.
Fig. 182a. The abdominal circumference is measured at the level of the umbilical portion of the
left portal vein. The diameters are measured from the skin surface.
It is most important that the scan shows a cross-section of the fetus that
is as round as possible. Make sure that the correct level is being
measured; look for the umbilical part of the left portal vein (see p. 256).
The measurement must be made on a true trans axial plane. where the
umbilical portion of the left portal vein enters and is entirely within the
liver. The vein should be short. not elongated. If it is too long. the axis
is too oblique (Fig. 182b).
Fig. 182b. An incorrect angle to measure the abdominal circumference: the abdomen does not
appear circular and the umbilical vein appears elongated.
When you have a scan at the correct level, measure the antero-posterior
(AP) and transverse diameters. A medium gain setting should be used
and the measurement must be from the outer edge of the fetal abdomen
on one side to the outer edge on the other side. Calculate the abdominal
circumference by multiplying the sum of the two measurements by 1.57.
Abdominal circumference =
(Antero-posterior diameter + Transverse diameter) x 1.57
If the abdominal circumference is less than the fifth percentile. it is
small. If it is greater than the 95th percentile. it is large. (With some
ultrasound units it is possible to make this measurement automatically
by tracing the perimeter of the abdomen.)
Obstetrics 239
240 Obstetrics
Feta//ong bone measurements
When measuring bone length. it is necessary to reduce the gain. It is
usually easy to see fetal long bones from 13 weeks onwards. Find a
projection that shows a transverse section of one of the long bones; then
scan at 90
0
to this to obtain a longitudinal section. Measurements are
made from one end of the bone to the other end (Fig. 183). The femur is
the easiest bone to recognize and measure. If there is any doubt. also
measure the limb on the other side.
The length of a bone. particularly the femoral length. can be used as a
measure of gestational age when the head measurement is unreliable
because of intracranial pathology. This occurs most frequently in the
third trimester.
Bone length may also be compared with gestational age or biparietal
diameter. A femoral or humeral measurement can be considered normal
if it falls within two standard deviations of the mean for the known
gestational age. It is proportional to the biparietal diameter if that
measurement falls within two standard deviations of the mean biparietal
diameter. A femur is short if it is more than two standard deviations
below the mean. A skeletal dysplasia is likely only if the femur length is
even smaller-5 mm smaller than two standard deviations below the
mean.
Fig. 183. The length of the femur is measured from end to end. In older fetuses (right), there is
an ossification centre at the distal end of the femur; this is not included in the measurement.
Recognition of intrauterine growth retardation
The differentiation between symmetrical and asymmetrical growth
retardation is important because they have different causes and different
prognoses, and require different management.
1. Symmetrical growth retardation-low-profile fetus. In the low-
profile fetus, (symmetrical) growth retardation is caused by a
chromosomal abnormality, infection or maternal malnutrition, and
becomes apparent earlier in gestation. The head: body ratio remains
within normal limits and the fetus is symmetrically retarded: all the
measurements are reduced in the same proportion.
2. Asymmetrical growth retardation-late growth deceleration. In
late (asymmetrical) growth retardation, the fetal insults occur later
in gestation (after the 32nd week) when fat accumulation should be
greatest. The abdominal circumference will be significantly lower
than normal and the head:body ratio will also be abnormal. Such
growth retardation results from placental insufficiency in mothers
with pre-eclampsia, oedema, proteinuria and hypertenSion. The
prognOSis for the fetus will be improved by adequate maternal
treatment.
See pp. 242-244 for the required measurements and quality control.
Obstetrics 241
242 Obstetrics
Measurements to assess fetal growth
A complete evaluation of fetal growth will require measurement of:
the biparietal diameter (BPD);
the head circumference;
the abdominal circumference;
the length of the femur.
What is the ultrasound-determined gestational age?
Comparison of fetal size and gestational age can provide a valuable
indicator of intrauterine growth retardation. During the first routine
scan, define the ultrasound gestational age based on the crown-rump
length, head measurement and femur length. For follow-up studies,
calculate age as the initial age (however derived) plus the number of
weeks intervening.
.. 'the first estimated gestational age is ,'.
>; based either on crown-rump length, or on head
or femur measurement.
"At-follow-up studies, gestational age is taken as
age at the initial study plus the
iii,n umber, ofweeks intervening.
Is the head size appropriate?
The head size (either biparietal diameter or head circumference) should
be appropriate for the estimated ultrasound gestational age, i.e. the
head measurement should fall within the range for the estimated
gestational age.
Using the biparietal diameter alone, about 60% of growth-retarded
fetuses will be detected. Using the abdominal circumference as well as
other measurements, the sensitivity increases to 70-80% .
Tables used to estimate gestational age, fetal
weight or be appropriate for
. ,the socialg'r<?up of the patient.
Is the abdominal size appropriate?
Measure the abdomen and determine the appropriate percentile. An
abdominal circumference less than the 5th percentile is abnormal and
suggests intrauterine growth retardation.
What is the fetal weight? In what percentile does the weight fall?
Determine the fetal weight from biometric tables using at least two
parameters and compare it with the standard distribution for the
estimated gestational age. Intrauterine growth is considered to be
retarded when the weight is lower than the 10th percentile. An abnormally
low weight of the fetus is usually observed after the abdominal
circumference and head:body ratio have become abnormal.
Is the head:body ratio normal, elevated or low?
The head: body ratio is calculated by dividing the head circumference by
the abdominal circumference. It should be remembered that
malformations may change the size of the head or abdomen. With
normal anatomy. the head: body ratio can be considered normal if it lies
between the 5th and 95th percentiles for the gestational age.
Head:body ratio = Head circumference
Abdominal circumference
The head:body ratio determines whether the growth retardation is
symmetrical or asymmetrical. If the fetus is small and the ratio is
normal, the fetus is symmetrically growth retarded. If the abdominal
circumference or weight is low and the ratio is elevated (greater than the
95th percentile), there is asymmetrical growth retardation.
Asymmetrical growth retardation is easier to diagnose than symmetrical
growth retardation.
Obstetrics 243
244 Obstetrics
Quality control
Fetal measurements should be accurate. Check your own performance
regularly to make sure that your examinations are consistent:
1. Make any of the required measurements. Take the transducer off
the patient. Repeat the measurement several times. Check the
variation between the results.
2. Make the three standard measurements (crown-rump length,
biparietal diameter and femur length). If possible, ask a colleague to
repeat the examination on the same day on the same patient.
Compare the results.
3. Compare your estimated delivery date with the actual date on which
the baby is born. Do this for several babies.
4. Do the quality control tests routinely, e.g. on the first Monday of
each month, or on some other easily remembered day (see also
pp.40-41).
Scanning a patient for another physician
If you scan patients for a referring doctor, you must inform him or her
of the range of accuracy of any information you provide. It is very
important to let the referring doctor know how much to trust the
ultrasound results.
Requests for specific measurements should not be carried out if the
results will provide misleading or inaccurate information. For example,
a request to measure the biparietal diameter at 36 weeks to determine
the exact gestational age is not acceptable, because the measurement
has a large range of variation at that time and the result will be
inaccurate. Choose whatever measurement is most appropriate for the
period of the pregnancy, and give the doctor the information required
after using the most accurate method.
There are limits to the accuracy of ultrasound.
Useclinical, laboratory and serial measurements
(at intervals of 2 weeks or more) when asseSSing
fetal development.
Normal pregnancy
Scanning a normal pregnancy must follow a strict routine, with
identification of uterine and fetal anatomy.
The following routine is recommended:
1. Survey the maternal lower abdomen and pelvis.
2. Locate the fetus.
3. Assess the fetal head (including the skull and brain).
4. Assess the fetal spine.
5. Assess the fetal chest.
6. Assess the fetal abdomen and genitalia.
7. Assess the fetal limbs.
Obstetrics 245
246 Obstetrics
Normal pregnancy
The first ultrasound examination should include a survey scan of the
whole of the lower maternal abdomen. The commonest finding is of
corpus lute urn cysts, which are usually less than 4 cm in diameter until
the 12th week (Fig. 184a). Very large cysts may rupture, causing
haemorrhage (Fig. 184b). There may also be torsion of the ovary.
The uterine adnexa and all the contents of the pelvis should be routinely
surveyed for any abnormality, particularly scarring, a large ovarian cyst
or large myoma (see pp. 21O-211) which may interfere with pregnancy.
If found, these should be measured and followed up (p. 235).
Fig. 184a. Typical appearance of a corpus luteum cyst in the right ovary, with an intrauterine
(8 weeks) gestational sac.
Fig. 184b. A large corpus luteum cyst (more than 4 cm) of the right ovary, with low-level internal
echoes. Although most likely due to haemorrhage, these echoes have no clinical significance.
Examine the uterus to:
1. Locate the fetus or fetuses.
2. Locate the placenta.
3. Determine the orientation of the fetus.
4. Estimate the amount of amniotic fluid.
Fetal head
. - - - . & --.: - .-" - -::-.. - A'
of ultrasound
is,the:assessmerit of the ,fetal head. -
.... - - .- ..
.. ,,' _11
Ultrasound can demonstrate the fetal head by the eighth week of
gestation, but intracranial anatomy becomes visible only after 12 weeks_
Technique
Scan the uterus to locate the fetus and the fetal head. Position the
transducer at the side of the fetal head and do axial sections from the
fetal vertex down to the base of the skull.
First locate the "midline echo", a linear echo that runs from the frontal
to the occipital fold of the fetal head. It is due to the falx cerebri, the
midline fissure between the two halves of the brain, and to the septum
pellucidum. Ifthe scan is just below the top of the head, the midline echo
appears to be continuous and is due to the falx. Lower down there is an
anechogenic rectangular area anteriorly in the midline which is the first
gap in the continuous midline echo. This is the cavum septi pellucidi.
Just behind and below this septum are two relatively anechogenic areas,
the thalami. Between them are two closely parallel lines , the lateral walls
of the third ventricle (these are seen only after the thirteenth week)
(Fig. 185).
Fig. 185a. The normal midline echo of the falx cerebri.
Fig. 185b. The cavum septi pellucidi at 21 weeks' gestation. The thalami are hypoechogenic.
Obstetrics 247
248 Obstetrics
At a slightly lower level. the middle of the lateral ventricle lines
disappears, but the frontal and occipital horns are still visible
(Fig. 186).
Fig. 186. Axial scan: at 20 weeks' gestation, the lateral margins of the frontal horns and the
medial margins of the occipital horns are visible.
The choroid plexuses will be seen as echogenic structures filling the
lateral ventricles. The frontal and OCCipital horns of the ventricles
contain fluid, but no choroid plexus (Fig. 187).
Fig. 187. Axial scan: the head of a normal fetus at 17 weeks' gestation showing the choroid
plexuses filling the lateral ventricles.
Scan 1-3 cm lower (caudally) close to the upper part of the brain stem
to locate a heart-shaped structure of low echogenicity with the apex
pointing OCCipitally. Just in front will be the pulsations of the basilar
artery and further forward again the pulsating circle of Willis should be
seen.
Posterior to the brain stem is the cerebellum. which is not always visible.
If the obliquity of the section is changed. the falx will still be visible
(Fig. 188).
Fig. 188. The cerebellum, cisterna magna, cerebral peduncles, and hypothalamus.
Below this the next scan will show the base of the skull which appears
x-shaped. The anterior branches ofthe cross are the sphenoid wings; the
posterior branches are the petrous pyramids of the temporal bones.
The ventricles are measured above the level of the BPD. Look for the
complete midline falx and then two straight lines that are close to the
midline anteriorly and move furth'er away posteriorly. These are cerebral
veins and mark the lateral wall of the lateral ventricles (Fig. 189).
Echogenic structures in the ventricles correspond to the choroid plexus.
Fig. 189. The cerebral veins appear as two almost parallel echogenic lines along the edges of
the lateral ventricles.
To assess the size of the ventricles. calculate the ratio of the width of the
ventricle to the width of a hemisphere at the widest part of the skull.
Measure the ventricle from the middle of the midline echo to the lateral
wall of the ventricle (the cerebral vein). Measure the hemisphere from the
midline to the inner table of the skull. The value of this ratio changes as
the fetus grows. but is normal if less than 0.33. Higher values need
to be compared with the normal range for the gestational age.
Ventriculomegaly (usually hydrocephalus) requires further investigation
and follow-up ultrasound. The infant should also be evaluated in the
early neonatal period.
Obstetrics 249
250 Obstetrics
In the front of the skull it is easy to recognize the fetal orbits; the lenses
of the eyes will appear as bright dots anteriorly (Fig. 190a). If the correct
scan can be obtained. the fetal face can be seen in the axial (Fig. 190b)
or coronal (Fig. 190c) planes. Movement of the mouth and tongue can
be observed after 18 weeks.
Fig. 190a. Axial scan showing the fetal orbits, the eyes and the lenses: the lenses are focally
echogenic. but the globes are otherwise anechogenic.
Fig. 190b. Axial scan showing the maxilla and overlying soft tissues.
If the position of the fetal head permits, make a sagittal scan anteriorly
to visualize the frontal bone, maxilla, mandible and mouth (Fig. 190c).
Fig. 190c. Sagittal (upper) and coronal (lower) scans: the lower part of the face is clearly seen.
Check that all the facial structures are symmetrical and appear normal.
looking especially for cleft palate (this usually needs considerable
experience) (Fig. 190d).
Fig. 190d. There is an asymmetrical cleft in the upper lip so that one side of the lip is much
larger than the other. Cleft lips can also be symmetrical.
Scan the posterior portion of the skull and neck to rule out the rare
meningocele or occipital encephalocele (pp. 263 and 264). Scanning
from the midline to the side can also rule out cystic hygroma (Fig. 191).
(Transverse scans of the posterior lower skull and neck are often easier.)
Fig. 191 . Sagittal scan: a septate cystic hygroma in the cervical region. The skull, vertebrae and
skin are normal.
Obstetrics 251
252 Obstetrics
Fetal spine
The fetal spine can usually be identified by the 12th week but can be
clearly seen from the 15th week of gestation onwards. In the second
trimester (12-24 weeks). the vertebral bodies have three separate ossifi-
cation centres: the central one will form the anterior mass of the vertebra
and the two posterior centres will form the laminae. These are seen as
two strongly echogenic lines (Fig. 192a, b and c).
Fig. 192a. Transverse scan: the cervical spine.
Fig. 192b. Transverse scan: the upper lumbar spine.
Fig. 192c. Transverse scan: the lumbosacral spine.
Although transverse scans will show the three ossification centres and
intact skin over the spine, longitudinal scans are needed throughout the
length of the spine to exclude defects or meningocele (Fig. 192d, e).
Coronal scans may show clearly the relationship of the posterior
ossification centres (Fig. 192t) .
Fig. 192d. Longitudinal scan: the fetal spine at 22 weeks' gestation.
Fig. 192e. Longitudinal scans: the lumbosacral spine (left) and the thoracolumbar spine (right).
The skin and the spinal canal can be seen.
Fig. 192f. Coronal scan: the lower lumbar and sacral spine. There is a double row of almost
parallel echoes arising from the posterior ossification centres.
Because of the curvature of the fetus, it is not
easy to perform a longitudinal scan of the entire
length of the fetal spine after 20 weeks.
Obstetrics 253
254 Obstetrics
Fetal chest
Transverse scans are the most useful for visualizing the fetal chest. but
longitudinal scans can also be helpful. The exact level can be determined
by recognizing the pulsation of the fetal heart.
Fetal heart
Fetal heart motion can be detected at 7-8 weeks' gestation but detailed
anatomy can be seen only after 16-17 weeks. The fetal heart lies almost
perpendicularly to the fetal trunk because it is pushed up by the
relatively large liver. A transverse scan through the chest images the
long axis of the heart and provides a view of all four cardiac chambers
(Fig. 193). The right ventricle lies close to the anterior chest wall and the
left ventricle close to the spine. The normal heart rate is 120-180 beats
per minute. but transient slower rates may occur.
Fig. 193. The fetal heart at 31 weeks' gestation. The four cardiac chambers. the septa and the
valves can be seen.
The cardiac chambers are about equal in size. The right ventricle is
round with a thick wall. the left ventricle is more oval in shape. The atrio-
ventricular valves should be visible and the intraventricular septum
should be intact. The fluttering valve of the foramen ovale should be seen
opening into the left atrium. (The heart is more clearly seen in the fetus
than postnatally because the fetal lungs are not aerated and the heart
can be scanned in different planes.)
Fetal lungs
The lungs can be seen as two homogeneous. moderately echogenic
structures on either side of the heart (Fig. 194). They are not well
developed until late in the third trimester and by 35-36 weeks their
echogenicity should equal that of the liver and spleen. When this occurs
it is probable that the lungs are reasonably mature. but maturity cannot
be accurately assessed by ultrasound.
Fig. 194. The fetal heart and lungs. The lungs are echogenic and homogeneous. The heart is in
early systole, so the atrioventricular valves are closed.
Fetal aorta and inferior vena cava
The fetal aorta can be seen on longitudinal scans (Fig. 195): look for the
arch (with its major branches), the descending and abdominal aorta,
and the bifurcation into the iliac vessels. The inferior vena cava can be
visualized as a large vessel entering the right atIium just above the liver.
Fig. 195a. The aortic arch and the thoracic aorta.
Fig. 195b. Coronal scan of the thoracic aorta. There are multiple shadows from the ribs.
Fetal diaphragm
On the longitudinal scans the diaphragm will show as a relatively
hypoechogenic band between the lungs and the liver, moving during
respiration. Both sides of the diaphragm should be identified. This may
be difficult because it is very thin (Fig. 196).
Fig. 196. The fetal diaphragm at 36 weeks' gestation: a thin anechogenic line separates the
heart and lungs from the abdominal viscera. The lungs and liver have different echogenicities.
Obstetrics 255
256 Obstetrics
Fetal abdomen
Transverse scans through the fetal abdomen are the most useful for
visualizing the abdominal organs.
Fetal liver
The liver fills the upper portion of the fetal abdomen. It is homogeneous
in echogenicity and, until the last few weeks of gestation, is more
echogenic than the lungs (Fig. 197).
Fig. 197. Transverse scan showing the fetal liver, which is homogeneous, the left portal vein,
spleen and the stomach.
Umbilical vein
The umbilical vein is seen as a small anechogenic tubular shadow and
can be traced from its entrance at the midline of the abdomen upwards
through the liver tissue and the portal sinus. The umbilical vein joins the
ductus venosus at the sinus, but the sinus is not usually visualized as
it is much smaller than the vein. If the position of the fetus permits, the
insertion of the umbilical cord on the fetal abdomen should be located
(Fig. 198).
....:I
Fig. 198. The insertion of the umbilical cord into the fetal abdomen, with the vessels continuing
on into the fetus.
Scan the fetal abdomen to visualize the site of cord insertion,
and to confirm the continuity of the fetal abdominal wall.
Fetal abdominal circumference
To obtain the circumference or the area of the fetal abdomen for the
estimation of fetal weight, measure on a scan that shows the inner end
of the umbilical vein at the portal sinus (see p. 239).
Fetal spleen
It is not always possible to image the spleen. When visible, it lies
posteriorly to the stomach and is a semilunar, hypoechogenic structure
(Fig. 197).
Fetal gallbladder
The fetal gallbladder cannot always be identified, but may be seen as a
pear-shaped structure lying parallel to the umbilical vein on the right
side of the abdomen (Fig. 199). Because they are close together in the
same plane they can be mistaken for each other. However, the umbilical
vein will pulsate and can be followed to other vessels. It should be
localized first. The gallbladder lies to the right of the midline and ends
at about a 40 angle to the umbilical vein. It cannot be traced from the
surface into the liver.
Fetal stomach
The normal fetal stomach appears as a fluid-filled structure in the left
upper quadrant of the abdomen (Fig. 200). It will vary in size and shape
depending on the ingestion of amniotic fluid (Fig. 197, 199,202): it is
normally very active with peristaltic movement. If, in a fetus of 20 weeks
or older, the stomach is not seen after 30 minutes' observation, it may
be that the fluid level is low, the stomach absent or malpositioned (e.g.
in a congenital diaphragmatic hernia), or the stomach and oesophagus
are not connected (e.g. in tracheo-oesophageal fistula).
Fetal intestine
Multiple fluid-filled loops of bowel can be seen in the second and third
trimesters. The colon is usually seen just below the fetal stomach, and
is predominantly anechogenic and tubular. Haustra may be identified.
The colon is best seen in the last few weeks of pregnancy.
/
Obstetrics 257
Fig. 199. The fetal abdomen:
the gallbladder, lying next to
the umbilical vein, is
anechogenic. The stomach
and liver can be seen.
Fig. 200. Transverse scan of
the fetal abdomen at the level
of the umbilical vein, showing
the stomach and part of the
aorta.
258 Obstetrics
Fetal kidneys
The kidneys may be imaged from 12-14 weeks onwards. but will only be
routinely seen clearly after 16 weeks. In transverse section they appear
as hypoechogenic. circular structures on either side of the spine
(Fig. 201). Within them can be seen the strongly echogenic renal pelvis;
the capsule is also echogenic. The renal pyramids are hypoechogenic
and can appear large. Some dilatation of the renal pelvis (less than 5
mm) may sometimes be seen but is a normal finding. It is important
to assess renal size by comparing the renal circumference with the
abdominal circumference.
The normal ratio between the kidney and abdominal
circumferences is 0.27-0.3.
Fig. 201. The normal fetal kidney in transverse (upper) and longitudinal (lower) scans: the
kidney tissue is hypoechogenic, but the renal capsule and pelvis are echogenic.
Fetal adrenal/suprarenal glands
The adrenals can be visualized only after the 30th gestational week. and
will then be seen as relatively hypoechogenic structures above the upper
poles of the kidneys. They are ovoid or triangular in shape and may be
up to half the size of the normal kidney (this is much larger than in the
neonate) (Fig. 202).
Fig. 202. Transverse scan: the fetal abdomen, showing the left adrenal gland and stomach.
Fetal urinary bladder
The bladder is a small ovoid cystic structure and can be recognized
within the pelvis as early as 14-15 weeks. If not immediately seen, it may
be identified on repeat scanning 10-30 minutes later. If the change in
size can be assessed, it should be noted that normal urinary production
at 22 weeks is 2 ml per hour. whereas at full term it is 26 ml per hour
(Fig. 203).
Fetal genitalia
Male genitalia can be more easily recognized than female. The scrotum
and penis may be seen as early as 18 weeks, but the female genitalia can
only be reliably identified after 22 weeks. The testes are seen in the
scrotum in the third trimester. unless there is a mild hydrocele (a normal
variation) in which case they may be seen earlier (Fig. 204a).
The labia majora and minora in the female become visible on the
transverse scan of the perineal area from 23 weeks onwards (Fig. 204b).
Obstetrics 259
Fig. 203. The fetal urinary
bladder shown as a cystic
structure within the fetal
pelvis.
Fig. 204a. The male
genitalia.
Fig. 204b. The female
genitalia at 28 weeks'
gestation. It is not always
easy to recognize the labia.
260 Obstetrics
Fetal limbs
The fetal extremities can be seen from the 13th week of gestation. Each
of the fetal limbs should be identified and the position, length and
movement noted: this examination can take quite a long time.
The ends of the fetal limbs are the most easily recognized. The proximal
bones can be clearly seen and the digits can be seen earlier than the
carpus and tarsus, which ossifY after birth. The fingers and toes become
identifiable after 16 weeks. Evaluation of the feet and hands for
anomalies is very difficult.
The long bones are dense compared with other structures. The femur is
the most easily seen because of the limited movement of the thigh; the
humerus is more difficult. The lower part of each limb (tibia and fibula,
radius and ulna) is the least easily visualized (FIg. 205).
Fig.205a. The normal fetal arm and hand. Fetal movement may make it difficult to see small
details of the limbs.
Fig. 205b. A full-length image of a fetal femur. The knee joint is flexed.
Fetal femur
The easiest way to find a femur is to scan longitudinally down the fetal
spine to the sacrum: one of the femurs will then be recognized. The
transducer should then be slowly angled until the entire length is
imaged and can be measured (see pp. 38 and 240).
When measuring the length of a bone, it is
important to be sure that the complete bone is
seen: if the scan is not along the axis, the
measurement will be shortened.
The abnormal fetus
Fetal anomalies
Neurological anomalies
Anencephaly
Hydrocephaly
Microcephaly
Encephalocele
Spinal anomalies
Myelomeningocele
Spina biflda
Cystic hygroma
Cardiac anomalies
Malposition
Ventricular septal defect
Hypoplasia
GastrOintestinal anomalies
Duodenal atresia
Jejunal atresia
Cardiac atresia
Abdominal wall defects
Omphalocele
Gastroschisis
Fetal ascites
Renal anomalies
Hypoplasia
Obstruction
Cystic disease ..
Amniotic fluid
Oligohydramnios
Polyhydramnios
Fetal death
Obstetrics 261
262 Obstetrics
Neurological anomalies
1. Anencephaly-absence of the vault of the skull and brain-is the
most common anomaly of the fetal central nervous system. It can
be recognized at 12 weeks' gestation; there will be hydramnios and
there may be other anomalies (Fig. 206). The a-fetoprotein is
usually elevated in the amniotic fluid and maternal serum (see also
pp.270-271).
2. Hydrocephalus can be recognized by the 18th week of gestation.
There will be dilatation of the anterior and posterior horns of the lateral
ventricles (Fig. 207a). For normal brain scans, see pp. 247-249.
Hyarocephalus due to the Arnold-Chiart malformation is associated
with a lumbar myelomeningocele. The frontal bossing gives the head
a characteristic shape which should always initiate a detailed
evaluation of the fetal head and spine, particularly if the maternal
serum a-fetoprotein is elevated.
Fig. 206. Anencephaly: the
face and the base of the skull
are visible, but the rest of the
head is missing. There is
excess amniotic fluid
(polyhydramnios).
Fig. 207a. Hydrocephalus:
the right lateral ventricle is
dilated and the choroid
plexus has dropped to the
dependent side.
Reverberation artefact
obscures the left lateral
ventricle.
Fig. 207b. Hydrocephalus,
due to Arnold-Chiari
malformation. The scan on
the left shows the
hydrocephalus; on the right is
the characteristic shape of
the head associated with this
malformation.
If the hydrocephalus is secondary to brain atrophy. the head is
usually smaller than normal (Fig. 207c).
3. Microcephaly. An abnormally small head can be diagnosed when
the biparietal diameter is more than three standard deviations
below the normal (see pp. 237-238). The biparietal diameter must
be measured. but it is also essential to calculate the head: body ratio
to exclude intrauterine growth retardation (see pp. 241-243).
Isolated microcephaly. without other anomalies. is rare and the
diagnosis can be difficult in borderline cases. Serial examinations
and very careful interpretation are necessary. Except when the head
is very small. do not diagnose microcephaly unless there are other
anomalies.
Be very cautious with the ultrasound diagnosis of
microcephaly. Serial examinations are essential.
4. Encephalomeningocele. This neural tube defect is characteristically
seen as a circular sac protruding from the bony calvaria and
containing fluid or brain tissue (Fig. 208). The occiput is the
commonest site. but anterior encephaloceles are common in some
ethnic groups. When asymmetrical, evidence of amniotic bands
should be sought. The commonest source of error is the similar
shadow caused by the fetal ear or by a limb alongside the head.
Repeat scans in different planes and at different times may be
necessary. Confusion may be caused by cystic hygroma. but the
calvaria will be intact. Encephaloceles may be associated with
infantile polycystic kidneys and polydactyly.
Recognition of neurological anomalies can be
extremely difficult.They should always be confirmed
by repeat scans and preferably by another observer.
Obstetrics 263
Fig. 207c. Microcephaly: the
fetal head is much smaller
than it should be for the size
of the body.
Fig. 208. An encephalocele
(containing both neural tissue
and cerebrospinal fluid)
protrudes in the midline
posteriorly.
264 Obstetrics
Spinal anomalies
Spinal anomalies are most common in the cervical and lumbar spine. The
soft tissue overlying the spine should be examined for continuity. and the
fetal spine for malformation. The fetal spine can be clearly seen from the
15th week of gestation onwards.
Myelomeningocele appears as a fluid-containing sac posteriorly. often
with neural elements (Fig. 209 upper). An open myelomeningocele may
have no sac. only disruption of the soft tissue over the defect: unraised
defects are the most difficult to detect. A bony abnormality can usually be
seen. Normally posterior ossification centres appear as two echogenic.
near-parallel lines. but spina bifida will cause the lines to diverge. On
normal transverse scans the posterior elements appear parallel; with
spina bifida. the posterior elements are laterally displaced. not parallel,
and pointing outwards (Fig. 209 lower) . Longitudinal scans are particularly
useful in detecting the protruding sac.
Not all degrees of spina bifida can be reco.ized by
ultrasound.
Cystic hygroma
Cystic hygroma is an abnormality of the lymphatic system. a cystic mass
with septations. found in the neck posteriorly. It may extend laterally
and anteriorly (Fig. 210), sometimes with a central septation or "spoke-
wheel" aspect. Unlike encephalocele or cervical meningocele. the skull
and spine are intact.
When cystic hygroma is associated with a generalized lymphatic anomaly
and fluid collects in the chest or abdomen. survival is unlikely.
Fig. 209. Coronal (upper)
and transverse (lower) scans
of a myelomeningocele.
There is a cystic mass
protruding posteriorly from
the lumbosacral spine. The
neural elements cause
internal echoes.
Fig. 210. A septate cystic
hygroma in the cervical
region. The skull. vertebrae
and skin are normal.
Fetal cardiac anomalies
The detection of most cardiac anomalies requires sophisticated equipment
and special training, including Doppler examinations. Malposition,
hypoplasia of one side and ventricular septal defects may be seen, but
if cardiac abnormalities are suspected, expert opinion should be obtained.
If referral is not possible, the obstetrician or attending physician should
be warned of the suspected abnormality and be present at the birth.
Fetal gastrointestinal anomalies
Congenital intestinal obstruction most commonly occurs either in the
duodenum or in the jejunum and ileum.
1. Duodenal atresia is the commonest anomaly of the gastrointestinal
tract. There will be two round cystic structures in the upper
abdomen of the fetus. The "cyst" on the left is the dilated stomach,
the one on the right is the duodenum. This is the "double-bubble"
sign. Hydramnios is present in 50% of the cases associated with
Down syndrome. and often there are also cardiac, renal and central
nervous system anomalies (Fig. 211).
Fig.211. Duodenal atresia. associated with hydramnios. Peristalsis could be seen in the
stomach and in the dilated proximal duodenum.
2. Jejunal-ilial atresia. The diagnosis may be difficult. Multiple cystic
structures will be seen in the upper fetal abdomen; these are dilated
loops of bowel (Fig. 212). They are not usually seen until the second
routine scan (in the third trimester). Hydramnios may be present
when there is obstruction high in the gastrointestinal tract, but not
when it is in the distal bowel. Associated anomalies are not as
common as with duodenal atresia.
Fig. 212. lIial atresia, causing marked dilatation of the small intestine.
If intestinal obstruction is suspected, repeat the scan in a few days
to confirm the fmdings.
3. Colonic obstruction or atresia. This condition is rare and the
diagnosis difficult to make with certainty with ultrasound.
Obstetrics 265
266 Obstetrics
Fetal abdominal wall defects
The commonest defect in the abdominal wall is in the midline
(omphalocele); this is often associated with other congenital anomalies.
Depending on the size of the defect. the hernia may contain part of the
bowel, liver. stomach and spleen. covered by a membrane of amnion
externally and parietal peritoneum internally. The umbilical vessels
usually insert into the hernia sac and can be seen spreading within the
sac wall (Fig. 213a).
Fig. 213a. Omphalocele (upper) and pseudo-omphalocele (lower). Upper: the liver and bowel
protrude through the defect where the umbilical cord is inserted into the abdominal wall. Lower:
the prominent bulge is the result of compression of the fetal abdomen; it later disappeared. The
antenatal diagnosis of an omphalocele must always be confirmed by scanning in different
pOSitions and at different times.
Other defects occur mainly in the right periumbilical region (gastroschiSiS) .
and are usually isolated. Only the bowel bulges through these
periumbilical defects and there is no covering membrane. Ultrasound
will show loops of bowel floating in the amniotic fluid outside the
abdominal wall. The umbilical cord inserts normally (Fig. 213b).
Fig. 213b. Gastroschisis: there is free-floating bowel. not covered by peritoneum, anterior to the
abdominal wall. The umbilical cord insertion is normal.
Fetal ascites
Free fluid within the fetal abdomen can be recognized ultrasonically as
an echo-free area surrounding the fetal viscera (Fig. 214). True ascites
surrounds the falciform ligament and the umbilical vein, but pseudo-
ascites is a hyopechogenic band surrounding the abdomen caused by
abdominal musculature and fat.
Fig. 214a. Fetal ascites, separating the liver from the abdominal wall. The skin is not thickened.
Fig. 214b. Hydrops fetal is: pleural effusions surround the echogenic lungs. The skin is
thickened.
When ascites is suspected, the fetal anatomy should be carefully
evaluated for associated anomalies. The major causes of ascites are
renal obstruction and hydrops. Since ascitic fluid may be urine, the
kidneys should be carefully scanned whenever there is ascites. Hydrops
fetalis should not be diagnosed with certainty unless there is thickening
of the skin (Fig. 214b, c) or more than one site of fluid collection (I.e.
ascites with pleural or pericardial effusions). The common causes of
hydrops are:
Rhesus isoimmunization or other blood incompatibilities.
Cardiac anomalies.
Cardiac arrhythmias (typically tachyarrhythmias).
Vascular or lymphatic obstruction (e.g. associated with cystic hygroma).
Fig. 214c. Hydrops fetalis: fetal ascites, separating the liver from the abdominal
wall. The skin is thickened and there is also fluid in the chest.
Obstetrics 267
268 Obstetrics
Fetal urinary tract anomalies
Some renal anomalies are invariably fatal and, if recognized before 22
weeks of gestation, can be an indication for therapeutic abortion (where
permissible). Recognition of the anomalies later in pregnancy can also
influence management.
Even if the kidneys appear normal in echogenicity, size,
shape and position, this does not exclude a urinary anomaly.
1. Renal agenesis (absent kidneys) syndrome. There is no amniotic
fluid and ultrasound is difficult. In the last few weeks of pregnancy,
the kidneys may be thought to be present because the adrenal
glands grow to a large size and become similar to the kidney in shape
(Fig. 215). The bladder is usually small or absent. Scan at many
different angles.
Fig. 215. Renal agenesis, with severe oligohydramnios. The large, hypoechogenic adrenal
glands have filled the renal fossae.
2. Hypoplastic (small) kidneys. Renal measurements may show that
the kidneys are small.
3. Renal obstruction; hydronephrosis. It is important to remember
that transient dilatation of the renal pelvis can occur. Such dila-
tation is usually bilateral but can be unilateral, and may persist for
some time (p. 258). Repeat the scan after two weeks. If the dilatation
of the renal pelvis is physiological, either there will be no change or
it may disappear.
If the dilatation is pathological, it will usually worsen (Fig. 216a).
Bilateral renal obstruction (hydronephrosis) is usually associated
with a decrease in the amount of amniotic fluid (oligohydramnios)
and has a poor outcome. Unilateral obstruction is not associated
with a decrease in amniotic fluid because the other kidney provides
adequate renal function.
In some cases there will actually be increased fluid (hydramnios).
On ultrasound, an increased cystic echo-free space will be seen in
the centre of the kidneys (or kidney) with smaller cysts budding
outwards. The presence of these small cysts (less than 1 cm) on the
cortical surface of hydronephrotic kidneys is a reliable but infre-
quent sign of dysplasia (Fig. 216a, b). Increased echogenicity and
diminished cortical thickness are less reliable signs of inadequate
function.
If the obstruction is at the level of the ureteropelvic junction, close
to the kidney, the renal pelvis tends to be rounded, and dilated
ureters will not be seen. When there is obstruction at the bladder
outlet (usually due to urethral valves in males), the bladder, as well
as both ureters and both renal pelves, may be dilated (Fig. 216c, d) .
Sometimes the distended posterior urethra may be seen as an
outpouching from the urethra.
Fig. 216a. Multicystic kidney with oligohydramnios: the cortical cysts were less than 1 cm in
diameter. There were other fetal anomalies.
Fig. 216b. Transverse scan showing bilateral hydronephrosis. The renal cortex is normal.
Fig. 216c. Coronal scan: bilateral hydroureter and hydronephrosis, caused by bladder outlet
obstruction. The bladder did not empty even after one hour.
Fig. 216d. Marked dilatation of the fetal bladder as a result of urethral obstruction. The kidneys
and ureters were dilated.
Obstetrics 269
270 Obstetrics
4. Multicystic kidney. Scans will show several cysts of different sizes,
usually scattered but rarely in one part of one kidney. The condition
is fatal if in both kidneys. Renal tissue may be visible between the
cysts, there is no clearly defined renal cortex, and the tissue will be
more echogenic than normal renal parenchyma (Fig. 217).
5. Autosomal recessive renal polycystic disease is not usually
recognized until the third trimester. A family history is usually
known and there will be oligohydramnios because of poor urinary
secretion. Both kidneys may be so large that they resemble the liver
except for their shape. The individual cysts are too small to be seen
by ultrasound, but there are so many interfaces that the kidney
becomes strongly echogenic (Fig. 218).
Amniotic fluid
1. Increased amniotic fluid (hydramnios. polyhydramnios).
Increased amniotic fluid may be seen in a number of conditions that
affect the fetus. The most common causes are:
Gastrointestinal obstruction (high jejunal or more proximal)
(Fig. 219).
Central nervous system anomalies and neural tube defects.
Hydrops fetalis.
Some abdominal wall defects.
Small-chested skeletal dysplasias (dwarfisms), which are usually
fatal.
Twins.
Maternal diabetes.
Fig. 217. A multicystic
kidney: the other kidney was
completely normal.
Fig. 218. Bilateral polycystic
kidneys at 34 weeks'
gestation. The kidneys are
hyperechogenic but the
individual cysts are too small
to be imaged by ultrasound
scanning.
Fig. 219. Polyhydramnios at
36 weeks' gestation. The
fetus had oesophageal
atresia.
2. Decreased amniotic fluid (oligohydramnios). Fetal urinary
secretion is mainly or entirely responsible for amniotic fluid
production from 18-20 weeks onwards. If there is bilateral renal
obstruction, dysplasia or non-functioning kidneys, the amniotic
fluid may be significantly diminished or absent (Fig. 220). This will
lead to pulmonary hypoplasia.
Fig. 220. Oligohydramnios. The fetal head and body are close to the uterine wall and placenta.
The urinary bladder is dilated as a result of outlet obstruction.
The etiology may be:
Rupture of the membranes with a leak of fluid.
Bilateral renal or urinary outlet anomaly (either urethral or
affecting both kidneys or ureters).
Intrauterine growth retardation.
Postmaturity.
Fetal death.
Obstetrics 271
of within the fetal abdomen are of renal origin.
',. may be unilateral or bilateral and. have non-communicating cysts.
, re(!essive (infantile) polycystic sol id echogenic
.. will not be recognized .
js a poor prognostic feature'whenthere is a fetal renal
it is associated with pulmonary insufficiency.
'. ":, '_' "',' _ _ _ -: :'::::: i'_'__ .
Fetal death
The diagnosis of fetal death is made when there is no cardiac motion.
There may be transient bradycardia or pauses in heart motion in normal
fetuses, and observation should last for several minutes. Other signs of
death are oligohydramnios and collapse of the skull with overriding of
the skull bones (Spalding's sign) (Fig. 221).
Fig. 221. Fetal death: the bones of the skull overlap, there is oligohydramnios and no cardiac
movement could be seen on real-time scanning.
272 Obstetrics
Placenta
Examination of-the placenta is an essential part
of any obstetric ultrasound examination.
The placenta is essential to fetal well-being, growth and development; it
can be demonstrated reliably and accurately by ultrasound. The exact
position can be determined relative to the fetus and the internal os of the
uterine cervix. The structure of the placenta and the utero-placental
junction can be assessed.
Uterine contractions can mimic the placenta or
a mass in the uterine wall (see p. 273).
Scanning technique
The patient should have a full, but not over-distended, bladder so that
the lower section of the uterus and the vagina can be clearly seen. Ask
her to drink 3 or 4 large glasses of water before the examination.
Multiple longitudinal and transverse scans will be necessary to
demonstrate the placenta completely. Oblique scans may also be
needed.
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Normal placenta
At 16 weeks' gestation the placenta occupies half of the inner surface of
the uterus. At 36-40 weeks' gestation, the placenta occupies 1/4 to
1/3 of the inner surface area of the uterus (see pp. 274-276).
Uterine contractions can mimic the placenta (Fig. 222a) or a mass in the
uterine wall (Fig. 222b) . Repeat the scan after 5 minutes, but remember
that contractions can last a surprisingly long time. If in doubt, wait
longer (p. 235).
Fig. 222a. On the left, the placenta appears to cover all the lower portion of the uterus. A later
scan (right) shows that the contraction had relaxed and the edge of the placenta is well away
from the internal os.
Fig. 222b. The scan on the left shows the placenta apparently raised by a mass; several
minutes later (right) the contraction has resolved and the mass has disappeared. Unlike a
myoma, a contraction is homogeneous, hypoechogenic and does not extend outside the uterus.
Accurate and prompt localization of the placenta ,
is very important in patients with vagi nal bleeding
or with signs of an unstable fetus, particularly in
the later stages of pregnancy_
An overdistended bladder can sometimes
produce a false impression of placenta praevia
(p. 274). Ask the patient to partially empty her
bladder and then repeat the examination. ;
Obstetrics 273
274 Obstetrics
Placental location
From 14 weeks onwards it is easy to locate the placenta (Fig. 223).
Oblique scans may be necessary for a posteriorly situated placenta.
Fig. 223. At 26 weeks' gestation the normal placenta is smooth and almost homogeneous.
The placental position is described in relation to the walls of the uterus
and the cervical os. Its position may therefore be right, midline or left.
If the placenta is free of the os, its position from front to back may be
described as anterior, anterofundal, fundal, posterofundal or posterior.
Placenta praevia
Identification of the internal cervical os is critical to the diagnosis of
placenta praevia. The cervical canal may be seen as an echogenic line
surrounded by two hypoechogenic or anechogenic lines, or it may be
entirely hypoechogenic (Fig. 224). The cervix and lower uterine segment
will appear different whether the bladder is full or empty. With a full
bladder the cervix appears elongated; edge shadows from the fetal head,
bladder or pubic bone may obscure some detail. When the bladder is less
full, the cervix changes orientation to become more vertical and
perpendicular to the sound beam. Although the cervix is more difficult
to find when the bladder is empty, itis less distorted, and the relationship
of the placenta to the internal cervical os can be more accurately
determined.
Fig. 224. The normal uterine segment and cervix: the cervical canal is hypoechogenic,
surrounded by two hyperechogenic lines. There is air in the vagina, causing bright echoes,
following a pelvic examination.
Placental position
1. If the placenta covers the os completely, there is central placenta
praevia (Fig. 225a).
2. If the edge of the placenta covers the os, this is marginal placenta
praevia (but the os is still entirely covered by the placenta)
(Fig. 225b).
3. If the lower edge of the placenta is close to the os, this is a low-Lying
placenta (Fig. 225c). This diagnosis can rarely be made with any
accuracy, since it is difficult to determine if only a part of the os is
covered by the placenta.
The location of the placenta may appear to change during pregnancy if
it is evaluated only when the bladder is full. Re-examination with a
partially empty bladder is necessary.
Placenta praevia may be identified during the early months of pregnancy
and not seen at term. However, a central placenta praevia recognized at
any time, or a placenta praevia identified at or after 30 weeks. is unlikely
to change Significantly. Provided there has been no bleeding in the
second trimester. a second routine scan can be delayed to 36 weeks to
confirm the diagnosis. If there is any doubt, the examination should be
repeated before 38 weeks or before labour.
Obstetrics 275
Fig. 225a. Central placenta
praevia: the os is completely
covered. The maternal urinary
bladder is full.
Fig. 225b. Marginal placenta
praevia: the internal os is
covered by the edge of the
placenta. The maternal
urinary bladder is empty and
the cervix lies almost
vertically.
Fig. 225c. Pseudo placenta
praevia: on the left, the
placenta appears to cover
the lower segment of the
uterus. After partial emptying
of the bladder (right), it can
be seen that the placental
edge is not near to the
internal os.
276 Obstetrics
Normal placental pattern
The placenta may be homogeneous or may have indentations or
echogenic foci along the basal plate (Fig. 226a). Echogenic septa extend-
ing across the width of the placenta may be seen in the later stages of
pregnancy.
Fig. 226a. A normal placenta.
Anechogenic areas immediately beneath the chorionic plate or within
the placenta frequently result from thrombosis and subsequent
accumulation of fibrin (Fig. 226b). When not extensive they can be
considered normal.
Fig. 226b. Large uterine vessels should not be mistaken for abruptio placentae. In this patient,
there is also thrombosis in the venous lakes below the chorionic plate.
Intraplacental anechogenic areas may be caused by moving blood seen
in dilated vascular spaces. If they involve only a small part of the
placenta, they are of no clinical concern.
Under the basal plate of the placenta, retroplacental hypoechogenic
channels may be seen along the wall of the uterus as a result of venous
drainage (Fig. 226c). This should not be mistaken for a retroplacental
haematoma (p. 278).
Fig. 226c. A normal placenta in late pregnancy. The surface has become lobulated. There are
retroplacental veins, which must not be mistaken for a haematoma.
Abnormal placental patterns
Hydatidifonn mole can be readily diagnosed by its typical "snow-stonn"
pattern (Fig. 227) (see p. 234). It is important to note that the fetus may
still be present and only part of the placenta may be affected.
Fig. 227. Transverse scan: the uterus is filled with speckled echoes, the "snow-storm"
appearance typical of hydatidiform mole.
Enlarged (thick) placenta
Measurement of the placental thickness is too inaccurate to influence
clinical decision-making. Any assessment can only be subjective
(Fig. 228).
1. Enlargement of the placenta occurs in maternal-fetal rhesus
incompatibility or hydrops.
2. Diffuse enlargement of the placenta may be seen in mild or moderate
maternal diabetes.
3. The placenta is usually large if there is an infection involving the
pregnancy.
4. The placenta may be large in abruptio placentae (see p. 278).
Fig. 228. A thick placenta (hydrops) due to maternal-fetal rhesus incompatibility.
Small placenta
1. The placenta is usually small and thin if the mother has insulin-
dependent diabetes.
2. The placenta may be small when there is maternal pre-eclampsia or
intrauterine growth retardation.
Obstetrics 277
278 Obstetrics
Abruptio placentae
Ultrasound is not a sensitive method for diagnosing abruptio placentae.
Characteristically, there is a hypoechogenic or anechogenic area beneath
or lifting the edge of the placenta (Fig. 229a). Blood may sometimes be
seen separating the membranes (see also p. 276) .
The haematoma may be echogenic and is sometimes so echogenic that
it blends with the normal placenta (Fig. 229b). Apparent thickening of
the placenta may be the only sign of a haemorrhage, or the placenta may
appear normal.
Ultrasound is not very accurate in the diagnosis
of abruptio placentae. The clinical diagnosis
remains very important.
Incompetent cervix
Any separation (widening) ofthe os, indicating incompetence, should be
identified. If there is fluid inside the cervix, the internal os may be
identified by small knuckles of tissue projecting towards one another at
right angles to the orientation of the cervix. The amniotic membrane may
prolapse (Fig. 230). The bladder should be emptied to take pressure off
the os, and a scan should determine if fetal parts or the umbilical cord
have also prolapsed. The patient's hips should be raised and she should
immediately be evaluated clinically.
Fig. 229a. A retroplacental
haematoma lifting the
margins of the placenta. The
haematoma eventually
resolved.
Fig. 229b. An echogenic
retroplacental haematoma
which blends with the
placenta. It is only because
the placenta appears so thick
that haemorrhage can be
suspected.
Fig. 230. An incompetent
cervix: the amniotic
membrane and fluid have
prolapsed into the vagina
through the open os.
The umbilical cord and vessels
The umbilical cord can be recognized in the first trimester. extending
from the chorion frondosum to the fetal pole (Fig. 231a). Longitudinal
and transverse scans will demonstrate one umbilical vein and two
umbilical arteries. If there are only two vessels. it is always an artery that
is missing: there will then be a high risk of perinatal mortality. and
anomalies will occur in approximately 20% of fetuses (Fig. 231b).
There is also a high risk of intrauterine growth retardation when there
is only one artery. Growth should be assessed at every scan (p. 242).
Multiple pregnancy
It is important to recognize each fetus and the position and number of
the placentas in cases of multiple gestation. A separating membrane
should be sought, usually most easily seen in the first or second
trimester. If the fetuses are of different sex. there is dizygosity. The size
of each fetus should be monitored to exclude a growth disturbance
affecting only one. The amount of amniotic fluid in each sac should also
be assessed (Fig. 232) (see also p. 231).
Obstetrics 279
the two umbilical arteries and
one vein found in a normal
umbilical cord.
Fig. 231 b. Transverse scan
of an umbilical cord with only
one artery and vein.
Fig. 232a. A first- trimester
twin pregnancy, divided by a
thin. but well defined
membrane.
Fig. 232b. A twin pregnancy
with two placentas.
separated by a membrane
which is only partially visible.
280 Obstetrics
Summary: scanning during pregnancy
Many physicians believe there is no reason for
any routine scans at any stage in a clinically
normal pregnancy, and scan only . when an
abnormality is suspected on clinical exam-
ination. Other physicians believe that two
routine scans are important for good antenatal
care (p. 225).
18-22 weeks' gestation
A scan at this stage will answer these questions:
1. Is it a single or multiple pregnancy?
2. Does the estimated age agree with the clinical gestational age?
3. Is the growth of the fetus normal for the gestational age?
4. Is the fetal anatomy normal?
5. Is fetal activity normal?
6. Is the uterus normal?
7. Is the amount of amniotic fluid normal?
8. What is the position of the placenta?
32-36 weeks' gestation
A scan at this stage will answer these questions:
1. Is the rate of growth normal for the period of gestation?
2. Is the fetus normal? Are there any developmental anomalies?
3. What is the position of the fetus (this may change before labour
commences)?
4. What is the position of the placenta?
6. Are there any complications, e.g. myomas, ovarian tumours, that
might obstruct delivery?
Late in pregnancy
If the patient has not had a previous ultrasound scan and is in the last
few weeks of pregnancy, a scan will answer these questions:
1. Is it a single or multiple pregnancy?
2. Does the fetal maturity match the clinical expectation?
3. What is the position of the fetus?
4. What is the position of the placenta? In particular, placenta praevia
must be excluded.
6. Are there any developmental anomalies?
7. Are there any complications, e.g. myomas, ovarian tumours, that
might obstruct delivery?
Ultrasound before and after external cephalic version
An ultrasound examination is often necessary immediately before
carrying out version from breech to vertex presentation to make sure
that the fetus has not already changed position.
Following the version, ultrasound is useful to confirm that the fetal lie
has become normal.
Ultrasound in early pregnancy (before 18 weeks)
If ultrasound scanning is considered necessary, it is preferable to wait
until 18-22 weeks of gestation because this will provide the most useful
information. However, there can be indications for ultrasound earlier
during pregnancy, such as:
1. Vaginal bleeding.
2. Patient does not know the date of her last menstrual period or there
is other reason for suspecting a discrepancy in dates.
3. There is no evidence of fetal life when expected.
4. There is a history of miscarriage, difficult labour or other obstetric
or genetic problems.
5. An intrauterine device is known to be in place.
6. There is a reason for terminating pregnancy.
7. The patient is unduly anxious about the pregnancy.
Ultrasound at mid-pregnancy (28-32 weeks)
It is preferable to wait until 32-36 weeks for any necessary ultrasound
examination, but there may be clinical indications for ultrasound earlier
than this, such as:
1. Clinical problems with the position or size of the fetal head.
2. Clinical examination suggests an abnormality.
3. An earlier ultrasound was not entirely normal or satisfactory.
4. The placenta was not accurately localized or was close to the os
during an earlier ultrasound examination.
5. The uterus is too large for the estimated gestational age.
6. fhere is leakage of amniotic fluid.
7. There is pain or bleeding.
8. The mother's clinical condition is unsatisfactory.
Obstetrics 281
282 Obstetrics
Indications and timing for additional ultrasound examinations
Ultrasound is unlikely to provide the explanation for
mild or moderate abdominal pain unless there is evidence
of pre-eclampsia.
The following may be indications for additional ultrasound examinations:
1. Intrauterine growth retardation: repeat ultrasound after 2 weeks.
2. Low-lying placenta: repeat at 38-39 weeks and again if necessary
before labour.
3. Abnormal presentation of the fetus: repeat at 36 weeks.
4. Discrepancy between the uterine size and gestational age: repeat at
36 weeks or earlier if the discrepancy is significant.
5. Known or strongly suspected fetal abnormality: repeat at
38-39 weeks.
6. Unexpected bleeding.
7. Lack of fetal movement or other evidence of fetal death: repeat
ultrasound immediately and if there is any doubt, follow with
further ultrasound in one week.
Ultrasound during labour
The indications for using ultrasound during labour are:
1. The pOSition of the fetus is unstable.
2. The fetal heart cannot be detected clinically.
3. There is a discrepancy in the size of the pregnancy and the size of
the fetus.
4. There is unusual bleeding.
5. Labour is delayed or is not following a normal clinical course.
Ultrasound in the postpartum period
There is no indication for a routine ultrasound examination following
parturition, but there are some clinical findings that may suggest that
ultrasound will provide further useful information.
In the immediate postpartum period:
1. Severe bleeding.
2. Retained placenta or torn placenta.
3. Undelivered twin or other fetus.
Six weeks postpartum:
1. Continued bleeding.
2. Persistent pain.
3. Failure of the uterus to return to normal size.
4. Continuous vaginal discharge.
5. Palpable mass in the pelvis.
CHAPTER 18
Neonates
Indications 285
Preparation for abdominal scans 285
Scanning technique: abdomen 285
Neonatal abdomen 286
Intracranial sonography 288
Hips 296
Neonates 285
Experience is needed to peform and interpret correctly all neonatal
ultrasound examinations.
Indications
Suspected anomalies of the:
1. Abdomen.
2. Head.
3. Hips.
For suspected pyloric stenosis. see p. 148.
Preparation for abdominal scans
1. Preparation of the patient. Clinical condition permitting. infants
should be given nothing by mouth for 3 hours preceding the
examination.
2. Position of the patient. The infant should
be supine (on the back) on a soft. comfortable
pillow. The arms should be lifted upwards
so that the abdomen is extended.
Cover the abdomen with coupling agent.
3. Choice of transducer. Use a 7.5 MHz transducer if available.
However. satisfactory information can often be obtained with a
5 MHz transducer. Small sector transducers are preferable as they
are more convenient for examining the small body of a neonate.
at the top of the abdomen (the xiphoid angle). Angle the beam
towalds the right side of the patient to image the liver. Adjust the
gain setting so that the image has normal homogeneity and texture.
It should be possible to recognize the strongly reflecting lines of the
diaphragm next to the posterior part of the liver and the portal and
hepatic veins should be visible as tubular structures with echo-free
lumens. The borders of the portal veins will have bright echoes. but
the hepatic veins will not.
Scanning technique: abdomen
Both transverse and longitudinal scans are required. As in the adult. the
aorta. inferior vena cava and portal veins should be identified (see p. 50).
7.5 MHz
or 5 MHz
286 Neonates
Neonatal abdomen
Indications
1. Abdominal mass.
2. Fever of unknown origin.
3. Haemolytic diseases.
4. Infections such as toxoplasmosis and listeriosis.
Liver
To see the whole liver as well as the liver parenchyma, the hepatic vein
and the portal vein, multiple scans in different projections are required
(Fig. 233).
Gal/bladder (jaundice)
It is not always possible to distinguish between biliary atresia and
neonatal hepatitis by ultrasound. Other causes of obstructive jaundice,
such as a choledochal cyst, gallstones or inspissated bile, can be
recognized. The normal neonatal gallbladder is 2-4 cm in length. It is
usually absent or small in extrahepatic biliary atresia, but may be
normal.
normal hepatic veins.
normal portal veins.
Fig. 234. Longitudinal scan:
normal gallbladder
in a neonate.
Blood vessels
It is important to demonstrate the major abdominal blood vessels and
their main branches (Fig. 235).
Kidneys
When scanning to exclude neonatal urinary disease, it is important to
remember that, until the age of 6 months, neonatal kidneys differ
acoustically from adult kidneys.
The difference between the renal cortex and medulla is less marked
in the infant.
The renal pyramids are relatively hypoechogenic and may resemble
cysts.
The renal cortex is less echogenic than the liver parenchyma.
As the child grows older, the difference between the cortex and the
medulla increases (Fig. 236).
Neonates 287
Fig. 235. Longitudinal scans.
Left: the aorta and superior
mesenteric artery. Right: the
inferior vena cava and right
atrium.
a kidney just after birth.
Fig. 236b. Transverse and
longitudinal scans of an
infant's kidney.
Fig. 236c. A kidney at the
age of 6 years.
288 Neonates
Intracranial sonography
Intracranial sonography is not an easy examination.
Indications for neonatal cranial ultrasound:
1. Hydrocephalus (a large head).
2. Intracranial bleeding.
3. Hypoxaemic damage.
4. Meningocele and other congenital anomalies.
5. Convulsions.
6. A small head (microcephaly).
7. Bulging fontanelles (raised intracranial pressure).
8. Trauma.
9. Intrauterine infection.
10. Mter meningitis, to exclude aqueduct stenosis or other sequelae.
Scanning technique
Usea 7.5 MHz transducer ifavailable; otherwise.
use a 5 MHz transducer.
Sagittal scan: centre the transducer over the
anterior fontanelle with the scanning plane
aligned with the long axis of the head. Angle the
transducer first to the right, to see the right
ventricle, and then to the left to see the left
ventricle.
Coronal scan: rotate the transducer 90 so that
the scan plane is aligned transversally, and
angle the beam forward and then backward.
Coronal scan
Axial scan: centre the transducer just above the
ear and angle the beam up towards the vault
and down towards the base of the skull. Repeat
on the other side.
Axial scan
1 st choice:
7.5 MHz
2nd choice:
5 MHz
L
Sagittal scan
Posterior coronal scanning
R
Normal midline anatomy
In 80% of neonates. the fluid-filled cavum septi pellucidi will be seen as
a midline structure. Below the cavum will be the triangular fluid-filled
third ventricle. and surrounding these structures will be normal brain
tissue of varying echogenicity (Fig. 237).
Fig. 237a. Midline sagittal scan: normal but premature neonatal brain.
Fig. 237b. Midline sagittal scan: normal full-term neonatal brain.
Fig. 237c. Angled left sagittal scan: normal lateral ventricle in a neonatal brain.
Fig. 237d. Midline coronal scan: the frontal horns of the lateral ventricles and the third ventricle
of a neonatal brain.
Neonates 289
290 Neonates
Sagittal section
Angled sagittal sections on each side of the brain
will show the lateral ventricles shaped like an
inverted "U". It is important to visualize the solid
thalamus and the caudate nucleus below the
ventricles because this is the region of the brain
in which haemorrhage is most frequent
(Fig. 238).
By angling the transducer, the entire ventricular
system can be examined.
The echogenic choroid plexus will be seen mainly
within the atria and the temporal horns.
Fig. 238a. Midline sagittal scan: normal neonatal brain.
Fig. 238b. Sagittal scan angled 20left: a normal neonatal brain.
Fig. 238c. Sagittal scan angled 30left: a normal neonatal brain.
Coronal section
Multiple scans should be perfonned at different
angles, depending on the individual patient, to
image the whole ventricular system and the
adjacent brain (see diagram, p. 288). Use the
most suitable angle for the particular part ofthe
brain to be examined (Fig. 239).
Fig. 239a. Coronal scan angled 10anteriorly: a normal neonatal brain.
Fig. 239b. Midline coronal scan: a normal neonatal brain.
Fig. 239c. Coronal scan angled 20posteriorly: a normal neonatal brain.
Fig. 239d. Coronal scan angled 30posteriorly: a normal neonatal brain.
Neonates 291
292 Neonates
Axial section
The first. most inferior. section will demonstrate the heart-shaped
pedicles and show arterial pulsation in the circle of Willis.
The next section above this will show the thalamus and the central echo
of the falx cerebri (Fig. 240a. b).
Fig. 240a. Axial scan from the right side: a normal neonatal brain.
Fig. 240b. Axial scan from the right side: the thalamus. falx cerebri and third ventricle.
The top (superior) section will show the walls ofthe lateral ventricles. The
ventricle and the corresponding hemisphere can then be measured
(Fig. 240c).
Fig. 240c. Axial scan from the right side: the lateral ventricles.
The ratio
ventricular
diameters
the hamllllDl'lartle
less than 1
cephalus nulSt .. '
Ventricular diameters 1
<-
Hemispheric diameters - 3
~ l
(1-----.. -;
--'(
hemispheric '
diameters
Ventricular dilatation
It is easy to recognize ventricular dilatation and asymmetry with
ultrasound. If in doubt. re-examination after an interval is essential.
One of the common causes of dilatation is congenital aqueduct stenosis
(Fig. 241a. b).
Fig. 241 a. Coronal scan: dilated frontal and temporal horns of the lateral ventricles and dilated
third ventricle.
Fig. 241 h. Sagittal scan angled 20to the left: marked dilatation of the left ventricle.
Agenesis of the corpus callosum is another congenital cause of
hydrocephalus. This causes marked lateral displacement of the lateral
ventricles and upward movement of the third ventricle (Fig. 241c).
Fig. 241c. Coronal scan angled 10posteriorly: agenesis (absence) of the corpus callosum.
Neonates 293
294 Neonates
Intracranial bleeding
1. Subependymal bleeding appears as one or more hyperechogenic
areas just below the lateral ventricle. best seen in a transverse plane
adjacent to the frontal horn. Confirm this with a sagittal scan: the
haemorrhage may be bilateral. This is a grade I haemorrhage
(Fig. 242).
Fig. 242a. Coronal scan angled 10anteriorly: grade I subependymal haemorrhage on the
right side.
Fig. 242b. Sagittal scan angled 20to the right: the same grade I haemorrhage as above.
2. Intraventricular bleeding into normal size ventricles. Additional
echoes from the normally echo-free ventricles (as well as from the
hyperechogenic choroid plexus) indicate thrombus (clot) in the
ventricles. If there is no ventricular dilatation. this is a grade II
haemorrhage (Fig. 242c).
Fig. 242c. Sagittal scan angled 20to the right: grade II haemorrhage into a normal-sized right
ventricle.
3. Intraventricular bleeding into dilated ventricles. When there is
intraventricular haemorrhage with ventricular dilatation. this is a
grade III haemorrhage (Fig. 242d).
Fig. 242d. Coronal scan angled 20posteriorly: grade III haemorrhage on the right side. The
left side is normal.
4. Intraventricular bleeding accompanied by bleeding into the
brain substance appears as areas of increased echogenicity within
the brain. This is a grade N haemorrhage, the most severe form
(Fig. 242e).
Fig. 242e. Sagittal scan angled 20to the right: grade IV haemorrhage.
5. Sequelae of bleeding. In grades I and II, the blood is usually
reabsorbed during the first week of life, but more severe bleeding
(grades III and N) can cause posthaemorrhagic hydrocephalus as
well as loss of brain tissue (porencephalic cysts). Developmental
retardation with abnormal neurological findings may result
(Fig. 243) .
Fig. 243. Coronal midline scan: right-sided porencephalic cysts and hydrocephalus, the
sequelae of a grade IV haemorrhage.
Neonatal cerebral abnormalities
Necrosis of brain tissue results in a poorly delineated region of
hypoechogenicity, usually lateral to the lateral ventricles (peri-
ventricular leukomalacia).
Cerebral oedema can result in obliteration ofthe ventricle and of the
cranial sulci. The brain is generally more echogenic than normal.
Cerebral infections cause changes in echogenicity, including punctate
hyperechogenic regions due to calcification.
Neonates 295
296 Neonates
Hips
Considerable skill and experience are needed to use ultrasound to
diagnose dislocation of the hips in the neonate. With practice, it is
possible to demonstrate the lower part of the iliac bone and the
acetabulum, particularly the roof ofthe hip joint and the rim ofthe fossa.
The exact position of the femoral head within the joint can be determined
and any discrepancy in the shape or size of the hip joint can be imaged
(Fig. 244).
Fig. 244a. Coronal scan: normal newborn hip. The midplane line of the iliac bone normally
bisects the femoral head.
Fig. 244b. Coronal scan: newborn hip, shallow acetabulum. The bony acetabulum is not as
deep as normal.
Fig. 244c. Coronal scan: subluxed newborn hip. The bony acetabulum is shallow and covers
less than 50% of the femoral head.
::;::,'::::; .... .' -' '
or very mild sonographic
a newborn infant, repeat the
hips will have
<.ltrfta ,-"', by tt,leh.
.'" -,'.,", '.
CHAPTER 19
Neck
Indications 299
Preparation 299
Normal anatomy 300
Abnormal thyroid 302
Other masses in the neck 306
Vascular abnormalities 307
Indications
1. A palpable mass in the neck.
2. Abnonnalities in the carotid arteries (a bruit or symptoms of carotid
insufficiency). Doppler ultrasound is needed for a complete
assessment.
(':-:P: ... -. _/ ,.'''' .. '" :.-" """: ...
is a way,. to':
. .'.. ..:
- . - - . .
Preparation
1. Preparation of the patient. There is no
specific preparation.
be lying on his or her back (supine) with the
neck extended over a pillow under the
shoulders. The pillow should be about
10 cm thick.
Apply coupling agent liberally to the neck.
linear transducer, if available; if not, use a
5 MHz linear or convex transducer.
4. Setting the correct gain. Vary the gain to
obtain the best image of the part being
scanned.
Scanning technique
Scans should be done in both longitudinal and
transverse planes, with oblique projections if
necessary.
During the examination, it may be necessary to
rotate the head from right to left, particularly for
vascular studies.
5 MHz 7.5 MHz
Neck 299
300 Neck
Normal anatomy
Ultrasound can demonstrate the folloWing normal structures in the
neck:
Carotid arteries.
Jugular veins.
Thyroid gland.
Trachea.
Surrounding muscles.
It is important that all of these structures are located when scanning the
neck.
1. Vessels. The vascular bundle (the carotid artery and the jugular
vein) is behind and between the sternocleidomastoid muscle and
lateral to the thyroid gland. These vessels are very accessible for
ultrasonography.
The carotid artery, bifurcating into the internal and external branches,
Will be seen as a tubular structure With hyperechogenic walls and
an echo-free centre: the walls are smooth and difficult to compress
With the transducer. The jugular vein is lateral to the carotid artery
and the walls are more easily compressed (Fig. 246). The veins vary
in diameter during the different phases of respiration and the
Valsalva manoeuvre.
2. Thyroid. The thyroid consists of two lobes,
one on either side of the trachea joined in
the midline by an isthmus. The thyroid
gland and the isthmus have the same
homogeneous echo texture, and the lobes
should be equal in size. On transverse scans,
the section is usually triangular; on
longitudinal scans, it is oval. The outline
should be smooth and regular.
The thyroid gland is normally 15-20 mm
thick, 20-25 mm in Width, and 30-50 mm
in length (Fig. 247) .
3. Muscles. The sternocleidomastoid muscle
is the only muscle of particular importance
in paediatric patients. The muscles are band-like structures which
are less echogenic than the thyroid (Fig. 245). On transverse scans,
the outline is well defined but varies from circular to ovoid in section.
4. Lymph nodes. Normal lymph nodes can sometimes be seen as
hypoechogenic structures less than 1 cm in diameter.
! 30-50 mm
0-25 mm
Fig. 245. Longitudinal scan: the thyroid gland and the sternocleidomastoid muscle. There are
two small cystic masses in the thyroid.
Fig. 246a. Longitudinal scan: the common carotid artery and the internal jugular vein.
Fig. 246b. Transverse scan: the common carotid artery, jugular vein, thyroid gland and
sternocleidomastoid muscle.
Fig. 247a. Transverse scan: the normal thyroid gland, including the isthmus.
Fig. 247b. Longitudinal scan: normal thyroid gland.
Neck 301
302 Neck
Abnormal thyroid
Thyroid abnonnalities may be local or diffuse. single or multiple.
Focal masses
1. Solid. About 70% of focal lesions are thyroid nodules and over 90%
of these will be adenomas. which are very seldom malignant. The
ultrasound appearance of an adenoma is variable and it may be
impossible to differentiate between a benign thyroid adenoma and
a malignant tumour: the ultrasound characteristics are similar.
and size is not important. Both benign and malignant tumours can
be hypo- or hyperechogenic; both may contain cystic components.
However. if the mass is well Circumscribed. with a surrounding thin.
hypoechogenic halo. there is a 95% probability that it is a benign
adenoma (Fig. 248a. b). When there is central necrosis. the possibility
of malignancy should be considered (Fig. 248c).
Fig. 248a. Longitudinal scan: an isodense nodule in the thyroid. surrounded by a
hypoechogenic halo.
Fig. 248b. Longitudinal scan: a benign thyroid adenoma with cystic changes.
Fig. 248c. Longitudinal scan: carcinoma of the thyroid with central necrosis.
2. Cystic. True cysts of the thyroid are rare. Characteristically. they
are well Circumscribed. with smooth walls. and are echo-free.
unless there has been haemorrhage into the cyst (Fig. 249).
Fig. 249. Longitudinal scan: a cyst in the thyroid.
3. Haemorrhage or an abscess may occur in the thyroid. appearing
as a cystic or complex pattern with ill-defined edges (Fig. 250).
Fig. 250. Longitudinal scan: a thyroid cyst partially filled with blood.
4. Calcification. Ultrasound shows hyperechogenic areas with distal
acoustic shadowing. Thyroid calcification is commonly seen in
adenomas. but may occur in malignant tumours. The calcification
can be isolated or in clusters. in groups or in chains. It is important
to remember that the size of the thyroid nodule and the presence or
absence of calcification are not evidence for or against malignancy
(nor will radiological examination provide a better differential
diagnosis) (Fig. 251).
Fig. 251 . Longitudinal scan: calcification in the thyroid gland.
-, - . .' .-
,A large thyroid gland with internal calcification mayor
;;:i may.lJpt ultrasound nor radiography
whetnertlle,massis benign or malignant.
. . !
Neck 303
304 Neck
Diffuse thyroid lesions
Homogeneous enlargement
The thyroid may be enlarged, sometimes extending retrosternally.
Enlargement may affect only part of a lobe, a whole lobe, the isthmus or
both lobes. Enlargement is usually hyperplastic and is ultrasonically
homogeneous. It may be due to endemic goitre, lack of iodine, puberty,
hyperthyroidism or hyperplasia following partial thyroidectomy
(Fig. 252a). A small, homogeneous, hypoechogenic thyroid may indicate
acute thyroiditis.
Fig. 252a. Longitudinal (upper) and transverse (lower) scans of homogeneous thyroid
hyperplasia. The gland is hyperechogenic because of iodine deficiency.
Heterogeneous enlargement
If the ultrasound density of the thyroid is heterogeneous, there are
usually multiple nodules (a multinodular goitre); the nodules may be
solid or complex on ultrasound. (Fig. 252b, c). In autoimmune thyroiditis,
the thyroid becomes heterogeneous and may resemble a multinodular
goitre.
Fig. 252b. Heterogeneous hyperplasia of the thyroid, without a cyst.
Fig. 252c. Heterogeneous enlarged thyroid with multiple nodules, some of which have
undergone cystic degeneration.
Neck 305
306 Neck
Other masses in the neck
Ultrasound is very useful in differentiating masses in the neck and
showing their consistency, shape, size, continuity, and relationship
with the thyroid and the vascular bundle. The etiology of such masses
is not always recognizable.
Abscess
The size and shape of a cervical abscess are very variable , and the outline
is often very irregular and unclear. On ultrasound, there are usually
internal echoes. In children, abscesses are most commonly in the
retropharyngeal region (Fig. 253).
Adenopathy
The diagnosis of enlarged lymph nodes in the neck is usually made
clinically, but ultrasound is a satisfactory method of follow-up. On
ultrasound, lymph nodes will appear as hypoechogenic masses with
regular outlines, solitary or multiple, nodular, oval or round, and
variable in size from 1 cm upwards. Ultrasound cannot determine the
cause of the lymph node enlargement (Fig. 254).
a retropharyngeal abscess in
a 4-year-old girl.
Fig. 253b. A lateral
radiograph of the neck,
showing the same abscess.
Fig. 254a. Multiple inflamed
cervical lymph nodes.
Fig. 254b. Enlarged inflamed
lymph nodes near the carotid
artery.
Cystic hygromas (lymphangiomas)
These are of variable size, are usually situated laterally in the neck, and
may extend to the thorax or axilla. On ultrasound they are flUid-filled,
often with septa (Fig. 255).
Fig. 255. A cystic hygroma in the neck of a child, with multiple fluid-filled spaces.
Less common neck masses
In children, echogenic masses may be due to haematoma (Fig. 256). In
the cervical muscles, a cystic or complex mass may be a thyroglossal
cyst (in the midline), a branchial cleft cyst (in the lateral neck) or a
dermoid.
Fig. 256. A haematoma in a child's neck.
Vascular abnormalities
It is possible with ultrasound to demonstrate atheromatous plaques and
show stenosis in the carotid artery, but it is not possible to evaluate
blood flow without Doppler ultrasound and, in many cases, angiography
(Fig. 257).
Fig. 257. Longitudinal scan: a calcified atheromatous plaque just proximal to the bifurcation of
the left common caroid artery.
Neck 307
308
Notes
CHAPTER 20
Pericardium
Indications 310
Preparation 310
Pericardial effusion 311
310 Pericardium
Indications
Suspected pericardial effusion. Echocardiography is a very specialized
technique. The use of a general purpose ultrasound unit should be
limited to the search for a pericardial effusion.
Preparation
is required.
examined lying supine (on his/her back)
and then in the sitting position.
Apply coupling agent over the cardiac area.
3. Choice of transducer. Use a 3.5 MHz transducer. Use a 5 MHz
Use the smallest transducer available to perform intercostal scanning.
at the top of the abdomen (the xiphoid angle). Angle the beam to the
right side of the patient to image the liver. Adjust the gain setting to
obtain an image with normal homogeneity and texture. It should be
possible to recognize the strongly reflecting lines of the diaphragm
next to the posterior part of the liver. The portal and hepatic vein
should be visible as tubular structures with an echo-free lumen .
The borders of the portal veins will have bright echoes, but t he
hepatic veins will not.
Scanning technique
Start with the transducer (with a small acoustic window) centrally in the
upper abdomen close to the edge of the ribs (the xiphoid angle).
Angle the transducer towards the head (cephalad) and ask the patient
to take a deep breath. This will usually show a transverse section of the
heart and the examination can be carried on through the respiratory
cycle. If the transducer is small enough to be applied between the ribs.
different sections can be obtained. There will usually be masking by the
ribs unless the transducer is very small. Blood is echo-free and the
cardiac walls are echogenic. The cardiac chambers vary in size depending
on the stage of the cardiac cycle (Fig. 258).
Fig. 258. Transverse scan: the normal heart in diastole.
3.5 MHz
adults
5 MHz
children
~ '
\ ( patient
( \ breathes in
~ ) - ~ \
patient
holds
angle breath in
transducer
Pericardial effusion
Fluid around the heart is seen as an echo-free region surrounding
the heart muscle (Fig. 259a). (Anechogenic fat anteriorly may resemble
fluid.) Ifthere is a small amount of fluid. it can be seen to change in size
and position as the heart beats. When there is a moderate amount of
fluid. the apex of the heart can be seen moving freely within the
pericardial fluid. Cardiac motion may be restricted by a large amount
of fluid.
It is not possible to distinguish serous from bloody effusions (Fig. 259b).
In malignant and tuberculous pericardial effusions. after the acute
stage, there may be localized or loculated effusions caused by adhesions
between the two layers of the pericardium (Fig. 259c). Internal echoes
in the effusion are due to infection or blood. Suspected calcification
within the pericardium is better assessed by radiography.
Fig. 259a. A large pericardial effusion.
Fig. 259b. Blood in the pericardium (haemopericardium) following trauma.
Fig. 259c. A large loculated pericardial effusion.
If pericardial calcification is
suspected, X-ray the chest.
Pericardium 311
312
Notes
CHAPTER 21
Pleura
Indications 314
Preparation 314
The abnormal pleura 315
------ - - - --- -
314 Pleura
Indications
Ultrasound can detect pleural fluid and may be helpful in localizing
small effusions when aspiration is indicated. If X-rays are already
available confirming the pleural fluid. the only reason to use ultrasound
is to guide aspiration when the fluid is loculated or there is only a small
amount (see pp. 318-319).
It is not necessary to use ultrasound to aspirate
every effusion.
Preparation
is required.
2. Position of the patient. Whenever possible.
the patient should be scanned while sitting
comfortably.
Apply coupling agent liberally over the lower
part of the chest on the side to be examined.
transducer. Use a 5 MHz transducer for
children or thin adults. Choose the smallest
transducer available in order to scan between
the ribs. If only a large transducer is available.
there will be shadowing from the ribs. but
information can still be obtained.
4. Setting the correct gain. Adjust the gain to
obtain the best image.
Scanning technique
The transducer should be centred between the
ribs and held perpendicular to the skin. Echo-
free pleural fluid can be recognized above the
diaphragm. lying in the pleural space. The lung
will be highly echogenic because of the contained
air (Fig. 260).
First scan the suspected area and compare with
X-rays if available; then scan at different levels
because the effusion may be loculated and is not
always in the lower pleural space (the
costophrenic angle) (Fig. 260c). Alter the patient's
position to see how much the fluid moves.
3.5 MHz
adults
5MHz
children
scan between ribs
The abnormal pleura
Pleural effusions are hypoechogenic or slightly echogenic. and sometimes
contain thick septa. Liquid blood and pus are also echo-free. but
septations may cause reflections (Fig. 260c). It is not always possible to
differentiate between fluid and solid pleural or peripheral lung masses
(Fig. 260d). Move the patient to a different position and rescan. Fluid will
usually move unless there is loculation or an excessive amount.
Peripheral lung or pleural masses do not move. Aspiration may be the
only way to establish the diagnosis.
Fig. 260a. Transverse scan: a moderate sized pleural effusion.
Fig. 260b. Longitudinal scan: a large pleural empyema on the right side.
Fig. 260c. A loculated. multiseptate right pleural effusion. the result of haemorrhage into the
pleural space.
Fig. 260d. A pleural mass (mesothelioma).
Pleura 315
316
Noles
CHAPTER 22
Ultrasound-guided needle
puncture
------ -
318 Ultrasound-guided needle puncture
Ultrasound gUidance is particularly important for biopsy of a small
tumour, or aspiration of a small effusion or abscess which is difficult to
localize clinically. It is not necessary to use ultrasound to aspirate every
effusion or ascites, but it is important when the fluid or tumour is close
to vital organs. Ultrasound should then be used to choose the shortest
and safest route for needle insertion.
Ultrasound is an ideal way to gUide a needle because the steel reflects
ultrasound and can therefore be clearly followed as it enters the body.
However, it is possible for only part of a needle to show. This can happen
if the front portion of the needle leaves the scanning plane and becomes
invisible. The apparent tip is then actually the point at which the needle
leaves the scanning plane and is not the actual tip of the needle. Not only
will this make it impossible to reach the required puncture site, but it
may cause damage by puncturing the wrong tissues. Fig. 261 illustrates
these difficulties.
Fig. 261a. An incorrectly angled scan: the point of the needle is not in the scanning plane and
is, therefore, not visible. As a result, the needle tip does not seem to have reached the target.
Fig. 261 b. A correctly angled scan of the same needle: the needle tip is now in the scanning
plane and is clearly visible beyond the target.
Fig. 261c. Scan of a needle which appears to bend, giving a false impression of the position of
the tip.
Images for Fig. 261a-c were obtained using a breast phantom.
There are devices to keep the needle in the
correct plane of the ultrasound by fastening it to
the transducer. When the needle is correctly
positioned, the transducer can be disconnected
leaving the needle in position.
It is always easier to guide a needle into spaces
filled with fluid (amniotic fluid, ascites, cysts,
abscesses, or pleural effusions) than into solid
tissue. The tip ofthe needle is not always clearly
visible in solid tissue: it may be recognized only
when moving and be very difficult to see when
stationary.
Fig. 262a. Needle aspiration of abdominal ascites, guided by ultrasound.
Fig. 262b. Needle biopsy of a mass in the liver, guided by ultrasound.
Ultrasound-guided needle puncture 319
Whenever possible, fluid should be aspirated from the centre of a cyst,
but the necrotic centre of a tumour should be avoided. The most
dependent region of pleural fluid should be chosen for aspiration. Once
the needle is correctly positioned, ultrasound should be used to monitor
the removal of the fluid or cyst contents.
- - I
If is very important that guided needle punctures are'
out in strictly sterile conditions.
320
Notes
ANNEX
Specifications for a
general purpose
ultrasound scanner (GPUS)
322 Specifications for a general purpose ultrasound scanner (GPUS)
Before purchasing an ultrasound scanner. it is essential to decide what
types of examination are to be carried out and then exactly what
equipment is needed (pp. 18-21). The minimum technical capability
expected should be made clear to any potential supplier. A WHO
Scientific Group has recommended minimum specifications for a general
purpose ultrasound scanner. Some scanners will exceed these
specifications but. for general use. any scanner that meets these
specifications will produce high-quality scans for all general purpose
examinations.
The original GPUS specifications were defmed in 1984.1 The technology
of ultrasound scanners has progressed significantly since then. and the
original specifications have been reviewed and updated. While there has
undoubtedly been progress. not all the new developments are cost-
effective or result in better patient care. Any benefits claimed for new
technology must be carefully assessed. Ifnecessruy. consult an expert
ultrasonologist who is aware of your needs.
It is unwise to accept any scanner that does not meet these minimum
specifications. even if it is less expensive. Any significant downgrading
of the specifications is likely to result in loss of qUality.
Specifications
1. The transducer design should be curvilinear (convex) or a combination
of linear and sector.
2. The standard transducer should have a central frequency of 3.5
MHz with accurate focusing. An optional transducer of 5 MHz is
desirable if it can be afforded. The 3.5 MHz is a fair compromise
between penetration and resolution. but the 5 MHz is very helpful
in scanning children. thin adults and superficial organs. It is a
worthwhile addition but should not replace the 3.5 MHz transducer.
3. The sector angle should be 40 or more. and the linear array should
be 5-8 cm long.
4. The controls should be simple and easy to use. Overall sensitivity
(gain or transmitter power) and time gain compensation must be
an integral part of the circuit. It must be possible to vary the time
gain compensation from a preset level. However. this is not essential
if the time gain compensation is at the correct level for obstetrics
with a preset alternative for the upper abdomen: then more than
80% of patients can be satisfactorily examined by varying the overall
gain only.
5. The frame rate must be 15-30 Hz for the linear array and at least
5-10 Hz for the sector array.
6. The frame freeze should have a denSity of at least 512 x 512 x 4 bits
(to provide 16 grey levels).
7. At least one pair of electronic omnidirectional calipers with
quantitative readout is reqUired.
8. It must be possible to add patient identification data (hospital
number. date of the examination. etc.) to the screen and the final
record.
9. It should be possible to obtain a permanent record (hard copy) ofthe
scan. The hard copy unit must work satisfactorily in the same
environment as the scanner (pp. 19 and 323).
10. There should be two or three imaging dynamics ranges available for
I WHO Technical Report Series, No. 723, 1985.
Specifications for a general purpose ultrasound scanner (GPUS) 323
post-processing. It is unnecessary to have a wider range of options.
11. The screen of the video monitor should measure at least
13 cm x 10 cm, preferably larger.
12. The equipment must be portable so that an average adult can move
it over at least 100 metres: if on wheels, these must be suitable for
rough irregular surfaces, but a unit that can be moved without
wheels is preferable.
13. The equipment must be suitable for the local climate, and be
protected against dust, damp, extremes of temperature, tropical
environments, etc. It should be possible to use the scanner
continuously within a temperature range of 10-40 C and 95%
relative humidity.
14. It must be possible to transport or store the unit safely under
adverse conditions. It should not be affected by air transport or
being moved across rough country in any vehicle. A specially
designed case for transport may be necessary.
15. It is essential that the scanner can operate from the local power
supply and is compatible with the voltage, frequency and stability
of the local current. The equipment should be able to stabilize a
voltage variation of 10%. If there is a greater fluctuation in the local
supply (and this should be tested before purchasing the unit), an
additional voltage stabilizer should be obtained. These voltage-
stability tests must be carried out before the scanner is accepted (see
p. 21). The equipment should conform to the standards set by the
International Electrotechnical Commission for medical electrical
equipment, and must be properly earthed (grounded).
16. Many ultrasound scanners incorporate biometric tables in the
microprocessor memory. These are useful, but care should be taken
to ensure that clinical measurements are made in exactly the same
way as was used to provide the tables. Biometric tables may not be
universally applicable and should be adjusted for local standards.
17. It is essential to ensure that servicing is available locally. No
ultrasound unit should be purchased unless there are trained
service engineers available in the vicinity. When in doubt, ask other
local users of ultrasound equipment about the quality of the service
and maintenance prOvided. This may well be the deciding factor
when choosing between scanners.
18. Service manuals and operating and maintenance instructions
should be provided at the time of purchase, especially if local
servicing is not readily available.
19. Accessories for ultrasound-guided puncture or biopsy must be easy
to sterilize.
The above speCifications will not be met by the cheapest and simplest
scanners. However, any unit that does comply with the GPUS
speCifications will be entirely suitable for all the examinations described
in this manual: that is, for 90-95% of the commonest ultrasound
examinations. More complicated investigations will require more
sophisticated and much more expensive scanners.
Further advice may be obtained from Radiation Medicine, World Health
Organization, 1211 Geneva 27, Switzerland.
324
Notes
Index
A
A-mode ultrasound 4, 5
Abdomen 47-51
abnormal 142-150
fetal 256-259
indications for scanning 49
neonates 285-287
preparation for scanning 49-50
scanning technique 51
Abdominal circumference, fetal (see also
Head:body ratio, fetal) 239,256
growth retardation 241, 242, 243
Abdominal masses 143-146
complex 144-145
fluid-filled 145
in bowel 143
outside bowel 144
Abdominal wall
artefacts 36
defects, fetal 266
Abortion
incomplete 233
spontaneous 232, 235
threatened 235
Abruptio placentae 278
Abscess
amoebic see Amoebic abscess
cervical 306
intra-abdominal 144-145,147,150
liver 78,79,86-88
pelvic 219, 220
perirenal 171
psoas 171
renal 167
splenic 131, 133
subhepatic 88
subphrenic 88, 133
thyroid 303
Acoustic coupling agent see Coupling agent
Adenitis, tuberculous 144
Adenomyosis, uterine 215
Adrenal (suprarenal) glands 156
carcinoma 69
fetal 258
masses 171
Air see Gas (and air)
Aliasing 7
Alveolar echinococcosis 146, 163
Amniotic fluid (see also Hydramnios) 270-271
Amoebic abscess
intra-abdominal 143, 144
liver 86,87,88
splenic 131
Amplification 11
Ampulla of Vater tumours 122
Amyloidosis 158
Anechogenic (anechoic) xi
Anencephaly 262
Aneurysm, aortic 58-59
Angiomyolipoma, renal 164
Aorta
abdominal 53-63,74
normal 56
preparation for scanning 54
scanning technique 54-55
aneurysm 58-59
bifurcation 54, 56
displacement 57
dissection 60
fetal 255
narrowing 61
neonatal 287
prosthesis 62
tortuous 61
Aortitis, idiopathic 54, 63
Appendicitis, acute 147
Aqueduct stenosis, congenital 293
Artefacts xi,32-39
Ascaris
biliary tract/gallbladder 98, 102
intra-abdominal 143, 144, 149
Aschoff-Rokitanski sinuses 104
Ascites 142-143,219
fetal 267
Aspiration
intraperitoneal fluid 143
pleural effusions 314,318,319
ultrasound-guided 38, 317-319
Attenuation xi, 11
Axial scan xii, 288
B
B-mode ultrasound 4, 5
Back wall effect xii, 32, 34
Basilar artery 248
Beam, acoustic xi, xii
distribution 27
focusing xii, 10, 29
Bile ducts
diameter, normal 109
dilated 108, 109, 110
jaundice 108, 109
normal 96
obstruction 98, 109
Biliary calculi (stones) 98, 110, 121
325
326 Index
Biliary tract 91-110
Bilomas 89
Biometric tables/measurements 23, 236-240
Biopsy, ultrasound-guided 38, 317-319
Biparietal diameter (BPD) 237,238
and fetal bone length 240
fetal growth assessment 242
microcephaly 263
Bladder 175-186
abnormal 178-186
blood clots 184
calcification 179, 182
calculi 182, 184
capacity 185
density within 182-184
diverticula 178
fetal 271
haematomas 180, 181 , 182
large (overdistended) 185
neurogenic 179
normal 177, 200
outlet obstruction 179, 280
polyps 180, 181, 182
schistosomiasis 179, 182, 186
small 186
tumour 180, 182, 186
wall thickening
generalized 178-179
localized 180-182
wall thickness 177
Bleeding see Haemorrhage
Blighted ovum 232
Blood clots, bladder 184
Bone
acoustic shadowing 12, 28, 35
measurements, fetal 240
Boundaries xii,12-13
Bowel
duplication 145
fetal 257
gas see Gas, bowel
ischaemia 145
masses 143-146
normal 141
tumour 143,144
BPD see Biparietal diameter
Branchial cleft cyst 307
Burkitt lymphoma 44, 158
c
Calcification
acoustic shadowing 35
aortic wall 61
bladder 179, 182
carotid 307
gallbladder wall 103
Calcification (continued)
pancreas 121
pericardial 311
thyroid gland 303
Calculi
acoustic shadowing 28, 35
gallbladder 100-102
kidney 169
ureteric 169, 172
urinary bladder 182, 184
Carbomers 45
Carcinoma
cervical 215
endometrial 214
Cardiac anomalies, fetal 265
Cardiac failure
gallbladder thickening 104, 105
hepatomegaly 76
vena cava dilatation 68
Carotid arteries 299
abnormalities 307
normal 300, 301
Caudate nucleus 290
Cavum septi pellucidi
fetal 40,247
neonatal 289
Cephalic index 238
Cerebellum 249
Cerebral
abnormalities, neonatal 295
infections, neonatal 295
oedema, neonatal 295
Cervical
abscess 306
carcinoma 215
lymph nodes 300, 306
Cervix, uterine 202
carcinoma 215
incompetent 278
Chest, fetal 254
Children (see also Neonates)
gastrointestinal symptoms 148-149
renal tumours 167
transducers for 20
uterus 199
Cholecystitis
acute 99, 104
chronic 104
Cholecystosis, hyperplastic 104
Choriocarcinoma 214, 234
Choroid plexus
fetal 248
neonatal 289,290,291
Circle of Willis 248, 292
Cirrhosis 78, 104, 109
macronodular 78
micronodular 80
Clonorchiasis 102, 110
Colitis, ulcerative 144
Colonic diverticulitis 144
Colonic obstruction/atresia, fetal 265
Colour Doppler 5, 8
Columns of Bertin, hypertrophied 165
Continuous wave Doppler 7
Contractions, uterine 235, 272, 273
Coronal plane xii,288
Corpus callosum, agenesis 293
Corpus luteum cysts 246
Couch, ultrasound room 21
Coupling agent xii, 43-45
application 44
ingredients/preparation 45
need for 13,26, 44
Cranial ultrasound see Intracranial sonography
CRL see Crown-rump length
Crohn disease 144
Crown-rump length (CRL) 236
Cul-de-sac, retrouterine, fluid in 142, 201
Cystic hygroma 307
fetal 251, 264
Cystitis 178, 186
Cysts xii,32-35
branchial cleft 307
dermoid 217
epididymal 192
follicular 209, 216
D
hydatid see Hydatid disease
kidney 162-163
liver 81-83
lymphatic 145
mesenteric 145
neck 307
needle aspiration 319
ovarian 209, 216-217, 246
pancreatic 120
porencephalic 295
renal 162-163
splenic 130, 131, 134, 135
thyroglossal 307
thyroid 303
Debris xii
Decubitus position, pancreatic scans 116
Dermoid cysts, ovarian 217
Diabetes mellitus, placental anomalies 277
Diaphragm 27, 50
fetal 267
Diverticula, bladder 178
Diverticulitis, colonic 144
Doppler effect 6
Doppler ultrasound 5, 6-8
carotid arteries 299, 307
clinical applications 7-8
"Double-bubble" sign 265
Duodenal atresia 265
Duplex Doppler system 8
E
Echinococcosis see Hydatid disease
Ectopic pregnancy 220, 222, 230
Effusion see Fluid
Electrical power supply 18, 21 , 323
Embryo 230
Empyema, gallbladder 99
Encephalocele 251,263
Encephalomeningocele 263
Endometrial carcinoma 214
Endometrioma 219
Endometriosis, uterine 215
Endometrium 198,212-213
Endovaginal ultrasound 197
Enhancement, acoustic xi, xii, 28
Epididymal cysts 192
Epididymis 189, 192
Epididymitis 192
Erect position 93
gynaecology 207
pancreatic scans 116-117
External cephalic version 281
Eyes, fetal 250
Face, fetal 250-251
Falciform ligament 74
Fallopian tubes 220
Falx cerebri
fetal 247,248,249
neonatal 292
Fatty liver 78
Female genitalia, fetal 259
Female pelvis see Pelvis, female
Femur, fetal 260
Femur length, fetal (FFL) 240, 260
Fetal anomalies 225,261-271
Fetal death 271 , 282
early pregnancy 232
Fetal weight estimation 243
Fetus
abnormal presentation 282
growth assessment 242-243
normal anatomy 245-260
sex determination 225, 259
Index 327
size and age estimation (biometry) 236-240
Fibroids, uterine 210-211
early pregnancy 235
Fibrosis, periportal 77
Filters, inferior vena cava 69
Fluid 28
amniotic 270-271
intraperitoneal (ascites) 142-143, 319
needle aspiration 38, 317-319
pelvis 219
pericardial 310,311
perirenal 171 , 173
pleural 88,133,314, 315, 319
retrouterine cul-de-sac 142, 201
within bowel 141
Focusing xii, 10,29
Follicles, ovarian 209
Follicular cysts 209, 216
Foreign body, bladder 184
Frequency, ultrasound xii, 29
Fronto-occipital diameter 242
Furniture, ultrasound room 21
328 Index
G
Gain xii-xiii,30-31
abdominal scans 50, 54, 66, 139
gallbladder scans 93
gynaecology 196
liver scans 72
neck scans 299
neonates 285
obstetrics 227
pancreatic scans 113
pericardial scans 310
pleural scans 314
renal scans 152
splenic scans 126
Gallbladder 75,91-110
absent 97
calculi 100-102
empyema 99
enlarged (distended) 98-99
fetal 257
fold 103, 105
internal echoes 100-103
jaundice 108
mucocele 99
neonatal 286
nonvisualization 97
polyps 103, 105
sludge 102
small 104
tumours 103, 105
wall thickening 104-105
wall thickness 95
Gallstones 98,99,100-101,102,103
impacted 103
Gas (and air)
artefacts 28, 36, 37
bladder 184
bowel 36, 141
aortic imaging and 55
pancreatic imaging and 113
Gastrointestinal tract 137-150
abnormal 142-150
fetal anomalies 265
masses 143-146
normal 140-141
paediatric disorders 148-149
Gastroschisis 278
Gel see Coupling agent
Genitalia, fetal 259
Gestational age 225
estimation in early pregnancy 228
fetal growth assessment 242
fetal measurements 236-240
Gestational sac 227-228
dimensions 228
small 232
Glomerulonephritis. 158, 168
Goitre 304"'-305
Granuloma, bladder 180, 182
Growth retardation, intrauterine see Intrauterine
growth retardation
Gynaecology (see also Pelvis, female) 195-222
Haemangioma, hepatic 85
Haematocolpos 213
Haematoma
bladder wall 180, 181, 182
intra-abdominal 145
kidney 170
liver 79,89
neck 307
perirenal 171
retroperitoneal 171
retroplacental 278
spleen 130, 134, 135
testis 193
Haematometrium 213
Haemorrhage
intracranial 294-295
sequelae 295
intrauterine, early pregnancy 235
thyroid 303
Hands/knees position 93, 101
Head, fetal 258-263
Head:body ratio, fetal
growth retardation 241, 243
microcephaly 263
Head circumference, fetal 238
growth assessment 242, 243
Heart
failure see Cardiac failure
fetal 232, 254
fetal anomalies 265
Heart rate, fetal 254
Hepatic cysts
complex 81
echinococcal (hydatid) 82-83, 86
multiple 81
simple SOlitary 81
Hepatic duct, common 96
diameter, normal 109
jaundice 108
Hepatic haemangioma 85
Hepatic veins 41,50, 73, 74
neonates 286
Hepatitis
acute 76
chronic 78
Hepatoma (hepatocellular carcinoma) 69, 84, 85
Hepatomegaly 76-79
homogeneous pattern 76-77
non-homogeneous pattern 78-79
tropical 76
Hepatorenal fossa 142
Hernia, inguinal 194
Hips, neonates 296
Histoplasmosis 132
Human immunodeficiency virus (HIV) infection
150
Hydatid disease (cysts)
alveolar 146, 163
biliary tract 98, 110
intra-abdominal 146
kidneys 163
liver 82-83, 86
pancreas 120
pelvis, female 218
spleen 130, 134, 135
Hydatid sand 82
Hydatidiform mole '234, 277
Hydramnios (polyhydramnios) 270
anencephaly 2.62
gastrointestinal anomalies 265
renal anomalies 268
Hydrocele 190,193
Hydrocephalus
fetal 262-263
neonatal 293
posthaemorrhagic 295
Hydronephrosis 160-161,221
fetal 268-269
Hydrops fetalis 267
Hydrosalpinx 213, 220
Hymen, imperforate 213
Hyperechogenic (hyperechoic) xiii
Hypertension, portal 129, 131
Hypertrophic pyloric stenosis 139, 148
Hypoechogenic (hypoechoic) xiii
Hysterectomy 203
Ileitis, regional 144
Iliac arteries 54, 60
normal measurements 56
Image
background 27
orientation 26
recording 19, 322
reversal xiii
Imaging, incomplete 38-39,318-319
Impedance, acoustic xi, xiii
Incomplete imaging 38-39,318-319
Inferior vena cava 65-69
abnormal 68
compression 68
dilatation 68
displacement, anterior 68
fetal 255
intraluminal filters 69
masses in 69, 166
neonatal 286
normal 67,74,115
Inguinal hernia 194
Interference pattern xiii, 27
Internal echoes xiii
Intestine see Bowel
Intracranial sonography 288-295
axial section 292
bleeding 294-295
cerebral anomalies 295
coronal section 291
indications 288
normal midline anatomy 289
sagittal section 290
ventricular dilatation 293
Index. 329
Intrauterine contraceptive device (IUD) 201
and pregnancy 229
Intrauterine growth retardation (IUGR) 241-243,
279,282
asymmetrical 241
symmetrical 241
Intrauterine haemorrhage, early pregnancy 235
Intraventricular bleeding 294-295
bleeding into brain with 295
dilated ventricles 294
normal size ventricles 294
Intussusception 149
Iodine deficiency 317
IUD see Intrauterine contraceptive device
J
Jaundice 107-110
bile ducts 108
biliary tract 109
differential diagnosis 107
gallbladder 109
Jejunal-ileal atresia 265
Jugular vein 300, 301
K
Kidney/abdominal circumference ratio, fetal 258
Kidneys 151-173
abscess 167
absent 157, 173
fetus 268
calculi 169
crossed ectopia 159
cysts
hydatid 163
multiple 162,163
simple 162
single large 162, 173
differential diagnosis of disorders 173
disease, chronic 104, 168
duplication 159
dysplastic 268
ectopic 157
fetal 258, 268-270
horseshoe 58
hypoplastic (small) 268
330 Index
Kidneys (continued)
irregular outline 173
large 158-163, 173
masses 164-167
L
complex non-homogeneous 166-167
solid 165
measurements 154
metastases 158
multicystic 162, 270, 271
neonatal 287
normal 154-155
polycystic see Polycystic kidney disease
small 168, 173
stone 169
trauma 170
tumour 69,164-167
Labour 282
Leishmaniasis 129
Lens effect xiii, 36
Leukaemia 129
Leukomalacia, cerebral, periventricular 295
Lighting in ultrasound room 21
Limbs, fetal 260
Linear array transducer 14, 15, 20
Liver 27, 71-89
abnormal 76-89
abscess 86-88
amoebic 86, 87,88
bacterial (pyogenic) 86,87,88
multiple 78, 79
caudate lobe 75
cystic lesions 81-83
enlarged (hepatomegaly) 76-79
fatty 78
falciform ligament 74
fetal 268
haematoma 79,89
lymphoma 79
masses
differential diagnosis 84
multiple echogenic 78-79
single solid 85
measurement 73
metastases 79,84
neonatal 286
normal 41,73,74-75
scanning technique 50, 73
small/shrunken 80
trauma 89
Long bones, fetal 240
Longitudinal scan xiii, xiv
Lungs, fetal 254
Lymph nodes
cervical 300
mesenteric 143
Lymphadenopathy, cervical 306
Lymphangioma, abdominal cavity 145
Lymphatic cysts 145
Lymphoma
abdominal masses 144
liver 79
renal 158
retroperitoneal 171
spleen 129, 132
M
M-mode imaging 5
Malaria 129
Male genitalia, fetal 259
Mass, complex (mixed) xiii-xiv
Meningocele 251,263,264
Menstrual cycle, endometrial changes 198, 212
Mesenteric cysts 145
Mesenteric lymph nodes 143
Metastases
hepatic 79, 84
renal 158
Microcephaly 263
Mirror effect xiv
Mole, hydatidiform 234, 277
Monitor 18, 323
Mononucleosis, infectious 129
Morrison's pouch 142
Mucocele, gallbladder 99
Multicystic kidney 162, 270, 271
Multiple myeloma 104
Multiple pregnancy 231, 279
Muscles, neck 300
Myelomeningocele 264
Myomas, uterine 210-211
early pregnancy 235
N
Neck 297-307
abnormalities 302-307
masses 302-307
vascular abnormalities 307
Needle puncture, ultrasound-guided 38, 317-319
Neonates (see also Children) 283-296
abdominal scanning 285-287
hips 296
intracranial sonography 288-295
Nephroblastoma 167
Nephropathy, obstructive 168
Nephrotic syndrome 158
Neurogenic bladder 179
Neurological anomalies, fetal 262-263
o
Obstetrics (see also Pregnancy) 223-282
transducers 20, 227
Obstructive nephropathy 168
Occipital encephalocele 251,263
Oesophagostomum 144
Oesophagus 140
Oligohydramnios 268, 271
Omphalocele 266
Ovarian vein, dilated 69
Ovaries
abnormal 216-218
cysts 209,216-217,246
follicles 209
identification and detection 197, 204-207
normal 208
postmenopausal 202
solid masses 218
Ovum, blighted 232
p
Paediatrics see Children; Neonates
Pancreas 111-123
calcification 121
common errors in scanning 123
cystadenoma 120
cysts 120
enlargement 119
normal 117-118
pseudocysts 120
small 118
tumours 98, 119, 122
Pancreatic duct
calculi 121, 122
diameter 118
dilatation 122
Pancreatitis
acute 119
chronic 118,119,121,122
Parietocolic gutters 142
Pelvic inflammatory disease (PID) 219
Pelvis, female (see also Ovaries; Pregnancy;
Uterus) 195-222
abnormal 210-222
abscess 219,220
endovaginal ultrasound 197
fluid in (ascites) 219
masses 219, 221
postmenopausal 202
varices 221
Pericardium 309-311
calcification 311
effusion 310, 311
Pericardium (continued)
Peristalsis, bowel 141
Peritoneal cavity 137-150
Periventricular leukomalacia 295
Pessary, vaginal 200
Phantoms xiv, 40
Placenta 272-279
abnormal patterns 277
enlarged (thick) 277
haematoma 278
location 274
low-lying 275, 282
normal 272-274
normal pattern 276
position 275
small ~
Placenta praevia 225,274-275
central 275
marginal 275
Index 331
Placental abruption (abruptio placentae) 278
Pleura 313-315
abnormal 315
Pleural effusions 314,315
aspiration 314, 318, 319
subphrenic abscess 88, 133
Polycystic kidney disease 158, 162, 163
autosomal recessive (infantile) 270,271
liver involvement 81
Polyhydramnios see Hydramnios
Polyps
bladder 180, 181, 182
gallbladder 103, 105
Porencephalic cysts 295
Portal hypertension 129, 131
Portal vein 50, 73
neonates 286
thrombosis 80
Positioning, patient
abdominal scans 49, 51, 54, 66, 138
bladder scans 176
gynaecological scans 196
liver scans 72
neck scans 299
neonates 285
obstetric ultrasound 227
pleural scans 314
renal scans 152, 153
scrotal scans 188
splenic scans 126
Postmenopausal women 202
Postpartum period 282
Pouch of Douglas (cul-de-sac), fluid in 142,201
332 -Index
Pregnancy 223-282
18-22 week scan 225, 226, 280
28-32 week scan 281
32-36 week scan 226, 280
abnormal 261-279
early (before 18 weeks) 227-235
abnormalities 232-235
gestational age estimation 228, 236
indications for scanning 224, 226, 281
intrauterine contraceptive device 229
ectopic 220,222,230
fetal size and age estimation (biometry) 236-243
first scan late 280
indications for additional scans 282
indications for ultrasound 224
intrauterine growth retardation 241-243
multiple 231,279
normal 245-260
safety of ultrasound 224
scanning for other physicians 244
survey scan 245
Preparation of patient
bladder scans 176
gynaecology 196
kidney scans 152
liver scans 72
neck scans 299
neonates 285
obstetric ultrasound 227
pleural scans 314
scrotum and testis 188
splenic scans 126
Probes, scanning see Transducers
Prostate, enlarged 178, 183
Prosthesis, aortic 62
Psoas abscess 171
Pulsed-wave Doppler 7
Pyelonephritis 158, 168
Pyloric stenosis, hypertrophic 139, 148
Pyometria 213
Pyosalpinx 220
Pyrexia 88, 133
Q
Quality control 40-41
fetal measurements 244
R
Real-time ultrasound 4, 5
Rectum 200
insertion of water into 207
Reflection xiv, 12
Refraction 12
Regional ileitis 144
Renal see Kidneys
Renal arteries 60, 155
stenosis 168
Renal capsule 155
Renal cortex 41, 155
Renal medulla 155
Renal pelvis (sinus) 155
fetal 258, 268
hydronephrosis 160-161
measurement 161
Renal vein(s) 155
thrombosis 168
tumour spread 166
Resolution 29
Retroperitoneal masses 171
Retroperitoneal sarcoma 144
Retropharyngeal abscess 306
Retroplacental haematoma 278
Reverberation xiv, 29, 37
Room, ultrasound scanning 21
Rubella 129
s
Sagittal scan XIII, XIV
Sand, hydatid 82
Sarcoma, retroperitoneal 144
Scanner see Ultrasound scanner
Scanning plane xiv
Scattering 13
Schistosomiasis
bladder wall thickening 179, 180, 182
late bladder changes 186
liver 77
splenomegaly 129
ureters 172, 179
Scrotum 187-194
abnormal 190-194
hydrocele 190-193
injury 193
normal 189
torsion 193
unilateral swelling 190-191
Sector scanners 14, 15, 20
Sensitivity 30-31
Servicing 18, 323
Sex, fetal 225, 259
Shadowing, acoustic xi, xiv, 12,28,35
Sickle cell disease 129, 131
Skin, transducer contact with 26
Solid xiv
Spalding's sign 271
Specifications, ultrasound scanner 321-232
Specular reflector xiv-xv, 13, 27
Spermatic vein, dilated 69
Spermatocele 194
Spina bifida 264
Spine
fetal 252-253
fetal anomalies 264
Spleen 125-135
abnormal 129-135
abscess 131,133
Spleen (continued)
accessory 135
common errors in scanning 128
cysts 130
congenital 130
hydatid 130, 134, 135
traumatic 134, 135
enlarged 129
fetal 268
haematoma 134, 135
infarct 132
masses 132
normal 128
trauma 130, 134-135
tumour 132
Splenic hilus 128
Splenic vein 114, 131
enlarged 131
Splenomegaly 129-131
tropical 129
Sternocleidomastoid muscle 300
Stomach 140
fetal 257
Strong back wall 32, 34
Strongyloides 144
Subependymal bleeding 294
Subhepatic abscess 88
Subphrenic abscess 88, 133
Superior mesenteric artery 41, 56, 114, 115
neonatal 286
Superior mesenteric vein 114
SJprarenal glands see Adrenal glands
T
Tampon, vaginal 200
"Target" sign 98
Teratoma, ovarian 217
Testis 187-194
mass 191
normal 189
small/absent 192
torsion 193
trauma 193
tumour 191
Thalamus
fetal 247
neonatal 290, 292
Thrombosis
portal vein 80
renal vein 168
Thrombus
abdominal aorta 58, 59
bladder 184
inferior vena cava 69
Thyroglossal cyst 307
Thyroid gland
abnormal 302-305
abscess 303
adenoma 302
calcification 303
cyst 303
diffuse lesions 304-305
enlargement 304-305
haemorrhage 303
mass, focal 302-304
normal 300, 301
tumour 302
Thyroiditis, autoimmune 305
Time-gain compensation (TGC) 11, 322
Tissues
effects on ultrasound 12
wave propagation 9
Transducers xv, 3, 14-15
bladder scans 176
choosing 20
convex 14, 15, 20
endovaginal 197
general-purpose 20
gynaecology 196
liver scans 72
mechanical 14
neck scans 311
neonatal scans 285, 288
obstetrics 20,227
paediatrics 20,285,288
pleural scans 314
renal scans 152
scan shapes 15
scrotal scans 188
sector 14, 15, 20
skin contact 26
splenic scans 126
standard 322
testing at delivery 22-23
types 14
variable focus 10
Transport, ultrasound scanners 18, 323
Transverse scan xv
Trauma
bladder 182
kidneys 170
liver 89
spleen 130, 134-135
testes 193
Tropical hepatomegaly 76
Tropical splenomegaly 129
Trypanosomiasis 129
Tuberculosis
bladder 180, 186
intra-abdominal 144
pelvic 219
renal 167, 168
spleen 132
Index 333
334 -Index
Tuberculous adenitis 144
Tumour, needle biopsy 318, 319
Typhoid 144
U
Ulcerative colitis 144
Ultrasound
basic scanning rules 26-41
basics 1-15
generators 3
modes 4-5
principle 3
scanning room 21
wave propagation 9
Ultrasound scanner 3
checks at delivery 22-23
choosing 17-23
complete unit 20
controls needed 18-19,322
electrical power supply 18, 21, 323
general-purpose (GPUS), specifications 321-323
quality control 40-41
servicing 18, 323
specifications 321-323
transport 18, 323
Umbilical arteries 279
Umbilical cord 279
insertion 256
Umbilical vein 256, 279
Ureterocele 183
Ureters 151-173
abnormal 172
calcification 172
calculi 169, 172
duplication 159
normal 155
Urinary bladder see Bladder
Urinary tract (see also Bladder; Kidneys; Ureters)
fetal anomalies 268-270
obstruction
fetal 268-269
hydronephrosis 160-161
Urine
extravasated 170
fetal production 259
residual 177, 185
Uterine cervix see Cervix, uterine
Uterus
v
abnormal 210-215
anteflexed 203
anteverted 203
bicornuate 212
contractions 235, 272, 273
developmental variants 212
double 212
empty, early pregnancy 233
enlarged 183
intrauterine device 201,229
large, early pregnancy 234-235
lining see Endometrium
malignant disease 214-215
measurement 198
multiparous 202
normal 198, 199
position 203
postmenopausal 202
prepubertal 199
retroflexed 203
retroverted 203
Vagina
insertion of water into 207
normal 198,199,200
Valsalva manoeuvre 67,74
Varices, pelvic 221
Varicocele 194
Vena cava, inferior see Inferior vena cava
Ventricle width/hemisphere width ratio
fetal 249
neonatal 292
Ventricles, cerebral
fetal 247,248,249
measurement 249, 292
neonatal 289, 290, 292
Ventricular dilatation, neonates 293
Version, external cephalic 281
Vesico-vaginal fistula 196
Video monitors 18, 323
Voltage stabilizers 21,323
w
Warranty, written 23,323
Wave propagation, ultrasound 9
Wavelength, ultrasound 9
Wilms tumour 167
Window, acoustic xi, xv
y
Yolk sac 231
Selected WHO publications
of related interest
Manual of radiographic interpretation for general practitioners.
P.E.S. Palmer et 01.
.1985 (216 pages)
Manual of darkroom technique.
P.E.S. Palmer
.1985 (25 pages)
Manual of radiographic technique.
T. Holm et 01 .
1986 (256 pages)
Maintenance and repair of laboratory, diagnostic
imaging, and hospital equipment
1994 (164 pages)
EHicacy and radiation safety in interventional radiology
2000 (96 pages)
EHective choices for diagnostic imaging in clinical practice.
Report of a WHO Scientific Group .
WHO Technical Report Series, No. 795, 1990 (131 pages)
Further information on these and other WHO publications can be obtained from
Marketing and Dissemination, World Health Organization, 1211 Geneva 27, Switzerland.
--
This manual provides guidance on the use of ultrasound in the diagnosis
of a wide variety of common conditions at the primary and first-referral
levels of health care. It is intended for use by doctors, sonographers,
nurses and midwives with basic training in ultrasound techniques, who are
working with a general-purpose scanner, and who do not have ready
access to expert advice.
The introductory chapters explain how ultrasound works, give advice on
choosing a scanner, and describe some misleading artefacts that may occur
on ultrasound images. These are followed by 17 chapters dealing with
specific organs or systems of the body. Each chapter includes guidance on
the indications for ultrasound examination, and describes the preparation
of the patient and the techniques that are likely to be successful. Numerous
ultrasound scans show both normal and abnormal conditions, and almost
every scan is accompanied by a corresponding computer-generated image
on which the most significant features are highlighted.
The manual has been prepared by an international group of radiologists,
physicians and physicists, who are all expert sonologists with wide
experience in both developed and developing countries. It is hoped that it
will contribute to a more rational use of this important imaging technique
and hence to improved care of patients.
ISBN 92 4 154461 9
~ ~

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