3

Prostate
Ragab Hani Donkol1 and Ahmad Al Nammi2
1Cairo
2Aseer

University
Central Hospital
1Egypt
2Saudi Arabia

1. Introduction
The value of prostatic sonography has dramatically increased in the past three decades.
Transrectal ultrasound (TRUS) imaging is currently an integral part of prostate cancer
diagnosis and treatment procedures, providing high-resolution anatomical detail of the
prostate region. In this chapter we review the anatomy and sonographic methods in
imaging of the prostate and prostatic diseases. Also we emphasize the role of new
sonographic techniques, such as color and power Doppler, the use of contrast agents, 3D
sonography and elastography for diagnosis of different prostate diseases especially prostate
cancer. We also discuss the use of systematic and targeted sonographic-guided biopsies as
gold standard for prostate cancer detection. Finally, we will elaborate the new role of
ultrasound in management of prostate cancer.

2. Anatomy of the prostate

2.1 Embryology of the prostate
In the 4th week of gestation, the urogenital septum divides the cloaca into two parts: The
rectum posteriorly and the primitive urogenital sinus anteriorly. In the 5th week, the distal
portions of the Wolffian canal and the Mullerian canal attach to the posterior aspect of the
primitive urogenital sinus (Fig. 1) to form an elevation called Mullerian tubercle. The
tubercle divides the primitive urogenital sinus into vesico-urethral canal superiorly and
definitive urogenital sinus inferiorly.The Wolffian canal forms the vas deferens, the ampulla
of the vas and the seminal vesicle. The Mullerian canal regresses to form the utricle.
Formation of the prostate begins at the 10th week of gestation by proliferation of the
epithelium of the posterior urethra around the orifices of the Wolffian canal, to surround the
urethral circumference. The prostatic glands formed anterior to the urethra regress and are
replaced by fibromuscular stroma. The secretory function of the glands starts about the 13th
week of gestation. (Brandes, 1989).
2.2 Gross anatomy of the prostate and its relations
The term prostate was originally derived from the Greek word prohistani , meaning to
stand in front , and has been used to describe the organ located in front of the urinary
bladder (Lowsley, 1912). The prostate is conical in shape with its long axis directed

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inferiorly and anteriorly. The shape and size of the prostate may vary with age. The prostate
of an adult man measures 20 25 gms in weight. The base of the prostate is directed
superiorly and in contact with the bladder base. The apex is directed inferiorly and in
contact with the external sphincter above the deep fascia of the urogenital membrane. The
anterior border is separated from the symphysis pubis and pubic bones by the retropubic
space which contains loose areolar tissue, preprostatic venous plexus, lymphatics, nerves
and puboprostatic ligament. The trapezoid area is an extraprostatic area of anatomic
weakness. It may be involved by carcinoma extending through the inferior neurovascular
pedicle. This area bounded by the prostate proximally, the rectourethralis muscle distally,
the membranous urethra anteriorly and the rectum posteriorly (Mayers et al, 1987).
Posteriorly, the prostate is related to the rectum and is separated from it by the Denovillers
fascia which extends superiorly, behind the seminal vesicles up to the peritoneal reflection.
At each posterolateral aspect of the prostate, the hypogastric pelvic fascia contains the
neurovascular bundle of the prostate, seminal vesicles and bladder neck (Fig. 2).
Ureter

Ureter
Mllerian
tubercle

Ureteric
bud

Wolffian
duct

Week 5

Week 25

Week 10

Urogenital
sinus

Tubular
urogenital
sinus

Wolffian
mesonephric
duct

Prostate

Mesenchyme

Week 7

Prostatic
epithelial
buds

Fig. 1. The embryological origin and development of the prostatic urethra and the prostate
(adapted from Delmas, 1991)

Fig. 2. Relations of the prostate in the coronal (A) and sagittal planes (B)
2.3 The distal seminal tract
It is formed of two seminal vesicles, ampullae of the vasa differentia and ejaculatory ducts.
The seminal vesicle is a cystic structure, measuring about 35 mm in length and 15 mm in
width. It is related anteriorly to the urinary bladder and posteriorly to the the rectum.The
ampula of the vas is located medial to the seminal vesicle. The vassal ampula joins the

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seminal vesicle to form the ejaculatory duct. Each duct enters the base of the prostate, passes
through central zone to end in the urethra below the utricle (Brandes, 1989).
2.4 Lobar concept of intraprostatic anatomy
In 1912, Lowsley demonstrated the first detailed description of the anatomy of the prostate.
This traditional concept which is no longer used, divided the prostate into lobes: an anterior,
posterior, middle and two lateral lobes. This method has been used to identify the prostate
and prostatic disease for about 60 years. The anterior lobe was situated from the anterior
margin of the gland to the level of the prostatic urethra. The middle lobe was a small area
between the proximal prostatic urethra and the ejaculatory ducts. This lobe extnds form the
base of the prostate to the level of verumontanum. The posterior lobe was situated posterior
to the ejaculatory ducts and extends to the posterior margin of the gland. The two lateral
lobes extend from the lateral margin of the gland bilaterally toward the middle part of the
gland. None of these lobes has clearly defined medial margin (Lowsley, 1912).
2.5 Zonal concept of intraprostatic anatomy
The understanding of the gross and microscopic anatomy of the prostate has changed
during the past few decades. Since 1965, a zonal concept of anatomy has evolved initially
developed by McNeal and then modified over about three decades. The prostate is best
considered to be a fusion of different glandular regions contained within a discontinuous
capsule (McNeal, 1968, 1988). The prostate is composed of four glandular regions and a nonglandular region which is the anterior fibromuscular stroma (Fig. 3). The fibromuscular
stroma (FMS) is the anteromedial portion of the gland is devoid of glandular tissue. This
region is generally considered to be of less clinical significance. The peripheral zone (PZ)
comprises the largest portion of the glandular prostate in young man (70%). The PZ is

Fig. 3. Zonal anatomy of the prostate in coronal and sagittal planes showing the central zone
(C), peripheral zone (P), transition zone (T) and anterior fibromuscular stroma (A). It also
shows the distal seminal tract formed of the ampula of the vas deference (d) which joins the
seminal vesicle (S) to form ejaculatory duct (e) which opens at vera montanium (v)
(adapted from McNeal 1968)

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situated posteriorly, posterolaterally and a thin layer of this tissue also extends up laterally
and anterolaterally. Distal to the verumontanum, the PZ often surrounds the urethra and
occupies the apical region if the prostate. The transition zone (TZ) is situated on both sides
of the proximal prostatic urethra and comprises only 5 to 10% of the glandular tissue in the
non hyperplastic prostate. The surgical capsule is an interface between the PZ and TZ. In the
aging prostate where the TZ can show marked glandular hyperplasia and may constitute
the majority of prostatic glandular elements. The periurethral glandular zone (PUG) consists
of mucosal glands in the prostatic urethra itself and represents only a tiny fraction of the
glandular prostate. This zone may become hyperplastic with age to form the median lobe
which may obstruct the bladder neck. The central zone (CZ) is cone-shaped with its base
forms the base of prostate, bordering the urinary bladder and seminal vesicles and its apex
is at the verumontanum The CZ forms about 25% of the glandular prostatic tissue. The CZ
surrounds the ejaculatory ducts throughout their entire courses in the prostate. The site
where the ejaculatory ducts enter the CZ is devoid of prostatic capsule. The extraprostatic
space invaginates around the ejaculatory ducts down to the verumontanum forming the
invaginated extra prostatic space . If the ejaculatory ducts are invaded by carcinoma, the
tumor will have a ready highway to the seminal vesicles and extraprostatic space.
2.6 Correlation of the lobar and zonal concepts of anatomy of the prostate
A comparison of Lowsley lobar and McNeal zonal concepts of anatomy is possible and
important to compare the clinical findings. Clinicians may still refer to lobar anatomy while
radiologists use zonal anatomy. So, the anterior lobe correlates with the anterior fibromuscular stroma. The medial lobe and the CZ are similar. The sum of the posterior and two
lateral lobes correlated to a large extent with the PZ.
2.7 Correlation of the zonal anatomy and origin of prostatic diseases
With the development of cross sectional imaging studies like transrectal ultrasound
(TRUS) and magnetic resonance imaging (MRI), the zonal concept of anatomy becomes
useful technique to apply because the different areas can be definite (Rifkin et al, 1990). The
zonal concept of anatomy is also useful because it incorporated a clearer understanding if
the development of disease. The origin of prostatic disease was poorly understood under
Lowsleys concept of lobar anatomy. It was previously thought that cancer only arises in the
posterior lobe and BPH develops predominantly in the lateral and, to a lesser degree in the
median lobe. It is now understood that the prostate cancer develops in the acinar tissue
predominantly the peripheral prostate. Although the PZ is three times larger in volume that
the CZ, prostate cancer develops seven times more often in the PZ. It was shown that about
50% of cancer arises in the anterior half of the prostate, including all those cancers from the
TZ (20% of the total), CZ (10%) and anteriorly situated portions of the PZ. In contrast, BPH
develops exclusively from the central gland, approximately 95% from the TZ and 5% from
the periurethral glandular tissue. Prostatitis (when not due to surgical manipulation) starts
mainly in the PZ similar to the prostatic cancer (McNeal et al 1988).

3. Techniques and approaches of prostatic ultrasonography

Ultrasonography is firmly established diagnostic tool in prostatic imaging. Recent
development in US technology has led to significant improvements in image quality,

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consistency and resolution. Additionally, dynamic scanners, color flow imaging and real
time imaging have allowed appreciation of blood flow, reduced examination time and
improved quality of the image. These advances combined with the portability, relative low
cost and lack of risks of iodinated contrast media and irradiation have made US one of the
most useful modality in evaluation of the prostate. Many approaches can be used to image
the prostate as trans-abdominal, trans-urethral, trans-perineal and transrectal US. The
common two approaches are transabdominal and transrectal ultrasound.
3.1 Trans-abdominal ultrasound
Transabdominal US of the prostate is nearly universally available and provides excellent
anatomic information using the urine-filled bladder as an acoustic window. Prostate size,
weight, shape and intravesical extent can be determined. Caudal angulation of the
transducer to accommodate the public bone is often required. The normal prostate appears
as a homogenous, round or ovoid structure with uniform low level echoes. The
intraglandular zonal anatomy can not be visualized (Fig. 4). The relation between the
prostate, bladder and seminal vesicles can be demonstrated (Abu-Yosef & Noryana 1982).

Fig. 4. Transabdonal US of a moderately enlarged prostate in axial and sagittal planes

3.2 Transrectal ultrasound (TRUS)
In 1963, Takahashi and Ouchi were the first to describe the use of TRUS to evaluate the
prostate. The first clinically applicable images of the prostate obtained with TRUS were
described in 1967 by Watanabe et al, they used a 3.5 MHz transducer, which at that time was
considered to be state of the art, to obtain images that were clinically meaningful. As US
technology has become more refined, the use of TRUS in the evaluation of prostatic disease
has increased. By the mid 1980s.TRUS had become a standard diagnostic instrument of the
urologists and radiologists. Most investigators today prefer equipment using hand-held
transducers which are available in frequencies ranging from 3.5 MHz up to 10 MHz with the
optimum frequency being around 7.0 MHz. Transrectal probes are available in different
sizes and shapes with diameters ranging from 1.2 to 2 cm.

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4. Sonographic anatomy of the normal prostate

Transrectal US of the prostate has revolutionized our ability to examine this organ. It
provides excellent visualization of the prostate in the axial and sagittal planes.
In the axial plane, scanning usually begins at a level just above the seminal vesicles and by
sequential withdrawing of the transducer in a caudal direction, the base, mid gland and the
apex is visualized (Fig. 5). When scanning the most cephalad areas, the vas deferens will be
visualized. They will appear as bilateral round cystic structures. Then the seminal vesicles
will come into view as the vas deferens joins with them superior to the prostate. They
usually appear as bow-tie configuration, but they may be rounded, lobulated or flattened.
At the level of the base of the prostate, the prostate appears as a symmetrical crescentshaped with triangular postero-lateral margin. The normal prostate will appear hyperechoic
to the sminal vesicles and will have a homogenous echopattern. The CZ and TZ cannot be
individually distinguished by their echogenicity. However the PZ appears more echogenic
with homogenous echotexture. At the level of mid gland, the prostate becomes ovoid in
shape. The anterior fibromuscular tissue is seem and has an echogenicity equal to or less
than that of the glandular areas. The hypoechoic periurethral glandular tissue is
demonstrated as hypoechoic area in the midline. Posterior and lateral to the PUG tissue, the
PZ appears more echogenic and homogenous. The apex of the prostate appears more
rounded. The obturator internus and levator anu muscles appear as hyperechoic structures
lateral to the prostate apex. The prostate is surrounded by hyperegenic layer comprising the
prostatic capsule and surrounding fat and fascia. The normal prostatic urethra is rarely
visualized. The advantages of axial scanning include visualization of the left-right symmetry
and echotexture,visualization of the anterior lateral portions of the PZ in a single view and
assessment the lateral extracapsular spread of carcinoma (Rifkin, 1997).
In the sagittal plane scanning starts in the midline where the entire prostate can be
visualized in one image. The seminal vesicle will be superior and posterior to the base of the
prostate, and the vas deferens will be seen anterior to the seminal vesicles. The seminal
vesicles will be less echogenic than the prostate and will appear rounded in shape. In the
midline sagittal plane, the hypoechoic periurethral tissue will be seen and may be difficult to
differentiate form the anterior fibromuscular stroma. The rest of the prostate will be
homogenous in echogenicity with the PZ slightly more echogenic than the CZ and TZ
(fig. 6). By tilting the transducer slightly to the right or the left of midline, the lateral aspects
of the prostate and seminal vesicles will be visualized. The lateral aspects of the prostate are
normally more rounded and homogenous in ehcogenicity. The ejaculatory ducts can be
identified as hypoechoic lines structures between two parallel echogenic lines as the course
from the seminal vesicles through the CZ into prostatic urethra. The advantages of sagittal
scanning include evaluation of the base and apex of the prostate in a single view, accurate
measurement of the cranio-caudal diameter of the prostate or of a lesion within the prostate
and better demonstration of the prostatic urethra and ejaculatory ducts ((Rifkin, 1997)
Estimation of prostate volume may be useful in a variety of clinical settings. In cases of BPH,
most urologists prefer to perform transurethral resections for glands under 60 grams, while
open prostatectomy is preferred for glands over 60 grams (Narayan & Foster 1991). Other
potential users include the comparison of the prostate volume with levels of PSA for early
detection of the prostatic cancer. PSA density is an index calculated by dividing PSA by the
volume of the prostate measured by TRUS. In absence of cancer, prostatic volume is directly

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Fig. 5. TRUS axial images. (A) the level of distal seminal tract; showing seminal vesicle (SV)
and vasl ampulla (V), (B) level of prostate base, (C) level of mid gland and (D) level of vera
montanum showing its appearance as tour Eiffel

Fig. 6. TRUS sagittal images; (A) in midline; (B ) in paramedical region; (C) peripheral part
of the gland which is formed mainly of peripheral zone (PZ) and above it the body of
seminal vesicle (SV) and (D) shows the confluence of vas and seminal vesicle (SV) to form
the ejaculatory duct (arrowhead)

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proportional to circulating serum PSA (Benson et al., 1992 ). Benign prostatic hyperplasia is
associated with, on average, only 0.26 ng/ mL PSA per gram of tissue, whereas cancer
results in a density 10-fold higher (Hammerer et al., 1995 ). Any PSA value greater than that
predicted by gland volume should raise a suspicion of prostate cancer. Also, the pretreatment estimation of the volume of prostate cancer can provide important prognostic
information after hormonal or radiation therapy. (Terris & Stamey 1991). The commonly
used method in measuring prostate volume is the elliptical method. This formula can be
transformed into volume = 0.523 x d 1 x d 2 x d 3. Maximal width and height diameters are
obtained at the largest appearing mid gland axial image section. The length dimension can
be obtained on midline sagittal plane (Fig. 9). This method is widely used because it is easy
and fast method. The fact that it is slightly less accurate than other methods is not
documented (Terris & Stamey,1990).

5. Diseases of the prostate and their sonographic appearance

5.1 Cysts of the prostate
Cysts of the prostate are confusing abnormalities because they are uncommon and their
origin is uncertain. Small cysts are asymptomatic while large cysts may present with
symptoms of urinary tract irritation, obstruction or hypofertility. The cysts may be
complicated by infection, and stone formation. They may be turned malignant in about
3% of cases (Litirup et al., 1988). The cysts are usually unilocular, sharply defined, thin
walled and anechoic. They vary size from 0.5 cm to 3.0 cm in diameters (Fig. 7). Prostatic
cysts are either midline prostatic cysts like utricle cyst and Mullerian duct cyst or lateral
prostatic cysts as cysts of the ejaculatory ducts or acquired cysts which are associated with
prostate cancer, PBH, and prostatic abscess (Patel et al., 2002). Utricle cysts are dilatation
of the prostatic utricle which may be congenital (megautricle) or acquired due to
obstruction of its orifice by inflammation (utriclocele). The utricle cysts are small
intraprostatic midline cysts.. Mullerian duct cysts are remnants of Mullerian duct. These
cysts are relatively large, extends superiorly and inferiorly from the level of the
verumontanum even outside the prostate. Ejaculatory ducts cysts are present along the
course of the ejaculatory ducts within the CZ. They are usually paramedian and
unilateral. They are complex cysts with solid and cystic components.They containing
spermatozoa. Extra-prostatic cysts are either cysts of the seminal vesicles or the ampulae
of the vas. They are congenital in origin and associated with urinary tract anomalies.
Some patients are manifested by obstructive azospermia and TRUS can classify the
patients without cysts where TRUS-guided aspiration and seminal vesiculography can be
performed and patients with cyst where TRUS-guided cyst aspiration and opacification
can be performed (Donkol, 2010).
5.2 Inflammatory diseases the prostate
Acute prostatitis is acute bacterial inflammation of the prostate. The clinical diagnosis
usually is not difficult. The patient has fever, perineal and low back pain; pain with
defecation of after ejaculation; urethral discharge associated with dysuria, urgency,
frequency, or retention. On examination, the prostate is swollen, boggy and tender. Griffiths
and associates in 1984 described three characteristic sonographic features seen in a group of
40 patients with an acute inflammation of the prostate as a periurethral echo-poor halo, a

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prominent periprostatic venous plexus and hypoechoic areas within the prostate,
predominantly in the peripheral zone (Griffiths et al., 1984).

Fig. 7. TRUS of different prostatic cysts. (A) Axial TRUS of a utricle cyst; the cyst is midline
and intraprostatic. (B) Sagittal TRUS of Mullerian duct cyst; the cyst is midline is midline
with supraprostatic extension. (C) Axial TRUS of bilateral seminal vesicles cysts in a patient
with obstructive azospermia. (D) Axial TRUS shows an acquired intraprostatic cyst in the in
the right part of adenoma of benign prostatic hypertrophy
Chronic prostatitis may be infective as a complication of acute prostatitis or noninfective
secondary to congestion of the prostate or urinary reflux into the prostate resulting in
inflammatory or fibrotic reaction or both within the prostate. Chronic prostatitis has varied
sympthomatology and lack of physical signs. The diagnosis currently rests on the finding of
excessive leukocytes in prostatic secretions. Sonographic findings include high density
echoes, mid range echoes, echo-lucent zones, ejaculatory duct calcifications, capsular
irregularity, capsular thickening and periurethral zone irregularity (Fig. 8 A&B). The
sensitivity and specificity of these signs are low (Doble & Carter, 1989)
Prostatic abscesses have been reported in an older age group due bladder outlet obstruction
and urinary tract infection. Iatrogenic prostatic abscess have been reported after biopsy or
instrumentation. Half of the patients presenting in acute retention and half presenting with
irritative voiding symptoms. Of the patients 40% have fever, 25% have associated
epididymo-orchitis. On examination, the majority showed enlarged prostate but only 20%
present with the classic signs of prostatic fluctuance and tenderness on DRE (Sohlberg et al.,
1991). Abscess can be identified as irregular hypoechoic area containing diffuse mid-range
echoes within an enlarged gland (Fig. 8 C). Once identified, the lesions may be aspirated
transperineally under ultrasound control (Doble & Carter, 1989).

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Fig. 8. (A) TRUS of a patient with chronic prostatitis shows calcification of periurethral
tissue. (B) TRUS of another patient with chronic prostatitis shows calcification of peripheral
zone. (C) TRUS of a case of prostatic abscess with a relatively thick wall and echogenic fluid
content. (D) TRUS of a patient with granulomatous prostatitis shows multifocal hypoechoic
lesions in the peripheral zone mimicking prostatic cancer
The exact aetiology of granulomatous prostatitis remains undetermined. It is thought to be
due to ductal obstruction and ectasia with subsequently extravasation of luminal contents
into the glandular stroma. In most patients, these changes are thought to be idiopathic but in
others, it can be also linked with specific infecting agents (tuberculosis, schistosomiasis, and
fungi). In patients with granulomatous prostatitis, the prostate is usually firm, nodular or
indurated on DRE, PSA may be elevated. Patients may present with symptoms of outflow
tract obstruction, acute retention or urinary infection. Sonographic findings are single or
multiple areas of low echogenicity in the peripheral zone (Fig. 8 D) or heterogeneous
echotexture of the gland. The hypoechoic areas are indistinguishable from carcinoma and
diagnosis must be established by biopsy (Clements et al., 1993).
5.3 Prostatic calcifications and calculi
Primary prostatic calculi develop in the prostatic ducts and acini. They are usually multiple
and small (1-5mms). Secondary dystrophic calcifications are associated with infection,
obstruction, necrosis in a prostatic adenoma or radiation therapy. They are usually larger
and more irregular than primary calculi. It needs to be emphasized that dystrophic prostatic
calculi are not precancerous (Hricak, 1990). Sonographically calcifications appear as bright
echogenic foci with or without posterior acoustic shadowing. Calculi can be seen within the
seminal vesicles, vassal ampulae or ejaculatory ducts (Fig. 9).

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Fig. 9. (A) TRUS shows multiple flecks of calcifications seen in both seminal vesicles (SV)
and vassal ampulae. (B) TRUS shows bilateral ejaculatory ducts calculi (arrow heads) in a
patient with obstructive azospermia

Fig. 10. (A) & (B) TRUS of BPH shows bilobed adenoma causing compression and flattening
of the PZ. (C) TRUS of another case of BPH shows calcified surgical capsule separating the
adenoma from the PZ. (D) TRUS of another patient with BPH shows large bilobed adenoma
separating from the flattened PZ by hypoechoic surgical capsule
5.4 Benign prostatic hyperplasia
Benign prostatic hyperplasia (BPH) is rarely seen in males less than 40 years of age. It affects
50 to 70% of men older than 60, and 80 to 85% of men older than 80 years. BPH begins in the
inner region of the prostate adjacent to the urethra. BPH may be diffuse or focal; forming
prostatic adenoma. The normal prostatic tissue is displayed caudally and posteriorly to form
the surgical capsule (Mc Neal, 1983). Ultrasound is the primary imaging modality for
evaluation of the aging men with known or suspected BPH. By transabdominal US prostatic

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size, weight, shape and intravesical extent can be determined. Uncomplicated BPH usually
produce a diffusely altered inhomogenous echotexture, but distinct nodular enlargement
cannot be differentiated from the surrounding gland (Fig. 5). Residual urine and bladder
volume can be measured by the same formula used for estimating prostatic size
(volume=0.52 x d1 x d2 X d3. Upper tract changes secondary to BPH are best evaluated
using abdominal US. TRUS provides the best cross-sectional anatomy of the prostate and it
is more accurate than transabdominal US to assess volume of the prostate and adenoma.
BPH has a varied echotexture but is usually homogenous solitary or multiple adenomas
(hyperplastic nodules) may be imaged, confined or extending outwards from the central
gland often compressing the peripheral zone (Fig. 10). Although symmetry is the rule
asymmetrical increase in size, especially near the bladder neck are common. Cysts,
calcifications, prostatitis, infarctions and carcinoma may be coincident with BPH. The thick
surgical capsule interposed between the central and peripheral gland can be appreciated.
(Naryan & Foster, 1991).
5.5 Prostatic cancer
Carcinoma of the prostate is the most common human cancer, found at autopsy in 30% of
men at age 50, 60% of men at age 80 90 up to 100% in those over age 90. It is now the
second most common cancer in men. Pathological evidence of prostate cancer is found in
10-20% of patients undergoing surgery for BPH. 68% of prostatic carcinomas originate in the
PZ, 24% in the TZ, and 8% in the CZ. Carcinoma of the prostate is often adenocarcinoma
with varying grades of differentiation in 95% (Mc Neal, 1983). Unlike lung and colon cancer,
prostatic cancer is predominantly latent. The patient may present with the symptoms and
signs of prostatism and occasionally haematuria. It has been speculated that prostatic cancer
disseminates first by invading into the periprostatic tissues, then by lymphatic embolization,
and finally by hematogenous dissemination. Prostatic cancer can also spread by direct local
invasion and through vascular and lymphatic channels. Seminal vesicle invasion almost
always results from direct spread of the tumor into the ejaculatory duct while crossing
inside and prostate. The primary field of lymphatic drainage of the prostate includes the
perivesical, hypogastric, obturator, presacral and preciatic lymph nodes. The obturator
nodes are the commonest site of involvement (Mc Laughlin et al., 1976). Osseous metastases
are present in about 85 percent of patients dying of prostatic cancer. Osseous metastases
involve the cancellous bone, altering the normal internal architecture with proliferating
osteoblasts and new bone formation. The commonest sites for visceral metastases from
prostatic cancer lung, liver and adrenal gland, but virtually any organ may be involved.
Pulmonary metastases, occurring in 25 to 38 percent of patients dying of prostatic cancer.
Metastases to the central nervous system usually occur in the meninges and may be
clinically silent. Other neurogenic manifestations of prostatic cancer include organic brain
syndrome, raduculopathy, and paraneoplastic syndromes (Jacobs, 1983).
5.5.1 Detection of prostate cancer
TRUS is useful for early detection of prostate cancer, guided biopsy, local staging, and
follow up after treatment. Its role in screening of asymptomatic men is still controversial.
(Clements et al., 1993).The first step in any sonographic examination of the prostate should
be to gain an overall impression of the glands shape and size. An irregular asymmetric

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gland often signals malignancy even in the absence of the identifiable lesion. Even small
prostatic cancer often alters the shape of the prostate. Distortion or bulging of the posterior
boundary of the prostate is suggestive of the presence of cancer. Lateral distortion is of less
significance because hyperplastic nodules of the TZ cause considerable asymmetric bulging.
In advanced cancer, discontinuity of the capsule or seminal vesicles irregularity often can be
seen (Shinohara et al.., 1989).
Prostate cancer has different echotexture; it may be hypoechoic, isoechpic or hyperechoic
(Fig. 11). Most cancers consist of a dense mass of cells which destroys the normal glandular
structure. The malignant tissue contains few sonographically detectable interfaces and
therefore appears hyperechoic region in relation to the adjacent normal tissue. The most
common feature of all visible cancer is a central hypoechoic region relative to the peripheral
zone of the normal prostate. The margins of the tumor all ill defined as the malignant cells
invade between normal prostatic acini (Shinohara et al., 1989). The hypoechoic tumors
represent 70-75% of prostate tumors (Hamper & Sheth, 1993). Approximately 30-35% of
clinically detected prostate cancer cannot be distinguished from the normal surrounding
prostatic tissue and is termed isoechoic. Several features may contribute to cancer being
undetectable by US: tumor size, grade, location, and stage, technique of the study,
equipment used and the experience of the operator. Absence of the normal margin between
the PZ and TZ in a rounded prostate should alert the sonographer to the possibility of a
large infiltrating tumor. Also, a palpable abnormality in the presence of an apparently
normal US scan should be biopsied to avoid missing an isoechoic cancer (Shabsigh et al.,
1989). In case of presence of large adenoma of BPH, the PZ is compressed. So, it is less easy
to detect a PZ cancer (Shinohara et al., 1989). Hyperechoic tumors are rare. Prostatic calculi
that have been engulfed by cancer may account for a mixed echogenic pattern. Hyperechoic
foci within the tumor correspond pathologically to comedonecrosis and calcification within
highly undifferentiated anaplastic tumors or unusual deposits of intraluminal crystalloid
secretions.
The sonographic appearance of early prostate cancer is not specific. The positive predictive
value for a hypoechoic focal lesion to be cancer has ranged from 0% to 50%. Overall, the
incidence of malignancy in US suspicious lesion is 20% to 255 (Hamper & Sheth, 1993).
Information from US-guided biopsy of the prostate has shown that many suspicious areas
seen on TRUS do not correspond to cancer: negative biopsy rated of 58 to 70.8% has been
reported (Shabsigh et al., 1989). There is a big list of differential diagnosis of intraprostatic
hypoechoic lesions. First anatomic structures as periurethral tissue, ejaculatory duct
complex, periprostatic veins and neuovascular bundles. Second are benign prostatic
diseases as hyperplastic nodule (stromal types), prostatitis, abscess, cysts and hematoma.
Lastly sonographic artifacts as inappropriate use of the focal range of transducer, acoustic
shadowing, reverberation artifacts and edge effect (Shinhara et al., 1989). Mc Neal and
associates have emphasized the importance of measurement of the volume of prostate
cancer as a determinant of pathologic stage and prognosis. They described a strong
association between tumor volume and the incidence of extracapsular extension and lymph
node metastases (Mc Neal et al., 1986). Estimation of tumor volume by TRUS is often
inaccurate for two reasons. Tumor size is usually underestimated, as the tumor tends to
infiltrate invade between normal prostatic tissues. So, the margin of the tumor may
therefore be indistinguishable from normal prostate. Second is prostate cancer is often

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multifocal. So, U.S underestimates the maximum diameter of a focus of cancer by an

average of 4.2 mm (Shinohara et al., 1989).

Fig. 11. TRUS of four different patients with prostate cancer. The carcinoma appears as focal
hypoechoic area (arrow head) in the right PZ (A), diffuse hypoechogenicity of the whole
gland (B), focal hyperechoic area (arrow head ) in the posterior PZ (C) and focal hypoechoic
area (arrow) in the central gland (D)
5.5.2 Extra capsular extension of prostate cancer
Prostate cancer spreads locally through pathways of least resistance. The areas of local
spread include the invaginated extraprostatic area around the ejaculatory duct to the
seminal vesicles, at the apex where the capsule is deficient, areas of capsule penetration by
superior and inferior neurovascular bundles. The prostatic capsule usually cannot be
distinguished sonographically from the prostatic parenchyma. Consequently, the continuos
hyperechoic border around the normal prostate, (usually referred as the capsule ), is
actually represents the acoustic interface between the prostate and the periprostatic fat
(Scardino et al., 1989). Sonographic signs of capsular penetration include bulge or
irregularity of the prostate contour and disruption or discontinuity of the echogenic
periprostatic boundary echo (Hamper & Sheth, 1993). Spread of the cancer to the
neurovascular bundle is suspected if the tumor is close to the posterolateral aspect of the
prostate with irregularity of the contour at this region as well as interruption of the
echogenic periprostatic boundary echo. TRUS is able to detect neurovascular involvement
with sensitivity of 66% and specificity of 78% (Fig. 12 and 13).

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Fig. 12. Two different patients with right and left lateral extracapsular extension (arrows)

Fig. 13. A case of prostate cancer with left posterolateral extension through the
neurovascular bundle (arrows)
The pattern and extent of seminal vesicle invasion vary widely. Type I is the most common
pattern. It shows invasion along the ejaculatory ducts into the seminal vesicle. Type II is the
second most common pattern. The invasion of seminal vesicle occurs from a tumor that
penetrates the capsule and invades the seminal vesicles in continuity. Type III is the least
common pattern, where small isolated foci of tumor in the seminal vesicles. The
sonographic criteria for seminal vesicles invasion have traditionally been described as
asymmetry in size, irregularity in outline, atrophy and distension, but the validity of these
signs has rarely been substantiated by surgical or pathological staging (Shinohora et al.,
1988). The accuracy of detection seminal vesicle invasion using sonography is 86% (Terries
et al., 1990). The apex of the prostate must be carefully assessed sonographically to detect
involvement of the rhamoboid area. This area bounded by the prostate proximally, the
rectourethralis muscle distally, the membranous urethra anteriorly and the rectum
posteriorly. It is best demonstrated by TRUS on the sagittal view. TRUS has no role in nodal
staging. Also, it had limited role in detection of invasion of neighboring tissue, e.g. bladder,
rectum and muscles of the pelvic side wall. These disadvantages of TRUS can be explained
by its limited field of view (Scardino et al., 1989).

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5.5.3 Response to treatment of prostate cancer

After treatment by ochidectomy and hormonal therapy, the gland becomes smaller and
assumes a more circular shape. Most of the decrease in volume occurred within the first
three months. A variable series of changes in the US appearance of the gland may be seen. In
some patients, the area of abnormal echogenicity may persist. In others, it disappears. The
integrity of the capsule may appear to be resorted in patients with previous capsule breech.
It may be extremely difficult to demonstrate U.S whether the active cancer is still present or
not (Clements et al., 1989). Following radiotherapy for cancer, the prostate becomes small
and echogenic. Anechoic or hypoechoic lesions following radiotherapy frequently represent
persistent cancer and the positive predictive value of such lesions for cancer is 91%. Most
foci of cancer with marked radiation effect tend to be isoechoic. The non malignant prostate
tissue generally retains its normal echogenic appearance after irradiation. Lesions over 5mm
in the diameter persisting for 12 months following radiotherapy are suspicious of
malignancy and should be biopsied (Egawa et al., 1991). A decrease in total prostate volume
is not a reliable indicator of prognosis as normal and malignant prostatic tissue will shrink
in response to radiotherapy. Measuring PSA is probably more useful in the follow up of the
prostate cancer (Richards, 1992). After radical retropubic prostatectomy (for clinically non
invasive prostatic cancer), the patients are routinely followed up at periodic interval with
DRE and measuring PSA. Elevation of PSA above the female range indicates either local
progression, recurrence of distant metastases. Post-operative mature fibrotic tissue at the site
of operation is difficult of distinguish form recurrent tumors by means of TRUS. The main
value of TRUS in case of presence of post operative palapable mass may be in accurate
positioning of the biopsy needle about the vesico-urethral anastomosis (Wasserman et.,
1992).

6. Ultrasound guided prostatic biopsy

The most important role for TRUS is to provide visual guidance for biopsy. Approximately
25% to 30% of cancers are isoechoic, random biopsies of the PZ, in addition to sampling all
suspicious lesions should be done. In the technique of random prostatic biopsies, multiple
samples are taken from different parts of the gland mainly apex, mid gland and base
bilaterally (Hamper & Sheth 1993). In general, TRUS guided prostate needle biopsy should
be performed in men with an abnormal DRE, an elevated PSA (>4.0 ng/ ml) or PSA velocity
(rate of PSA change) >0.4 to 0.75ng/ ml/ yr. Also, men who were diagnosed with high-grade
prostatic intraepithelial neoplasia (PIN) or atypia on a previous prostate needle biopsy
should undergo a repeat biopsy 3 to 12 months later. Less commonly agreed upon
recommendations for TRUS guided prostate needle biopsy include, age-specifi c PSA
elevation, low percentage free PSA (< 22% to 25%), and prostate specifi c antigen density
(PSAD) > 0.15, which is a measure of the amount of PSA relative to the overall prostatic
volume (Hamper & Sheth 1993).US- guided prostate biopsies can be performed either
transperineally or transrectally.
Transperineal approach is the first way described for US-guided prostate biopsy in 1981.
The probe is fixed to a stabilizing biopsy stand. The perineum should be infiltrated local
anesthetic. The entire gland is inspected and once a suspected area is identified, the biopsy
needle is inserted and the track of the needle is monitored on the viewing screen. When the

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needle tip approaches the area to be biopsied, the needle is positioned so that the cutting
section can be passed through the abnormal area under visual guidance (Muldoon &
Resnick, 1989). The drawbacks of transperineal U.S guided biopsy are difficult needle due to
relatively long transperineal needle path, it is time consuming procedure, and patients
tolerate the procedure poorly because of perineal pain and side effects of local anaesthesia.
(Clements et al., 1993). Transperineal approach is preferable if prostate abscess or
inflammatory disease is suspected.
Transrecta approach was first described in 1987, since then, this technique has been
described as a superior method of performing a core biopsy of the prostate (Weaver et al.,
1991). The transrectal approach offers the advantage of a shorter needle with easier needle
placement, and quicker and relatively painless procedure. Local anesthesia is not required
and it is done on an out-patients basic (Clements et al,. 1993). Hodge et al reported that
systematic sampling of the prostate guided by TRUS improved the detection rate of prostate
cancer over merely sampling hypoechoic or other lesions. By taking sextant biopsies from
the mid lobe (parasagittal) of each side of the prostate at the apex, middle, and base (Fig. 14),
the cancer detection rate was superior to lesion-directed biopsies (Hodge et al., 1989). This
technique was accepted over the time as the standard of care and helped to emphasize that
TRUS was more useful for biopsy than for imaging. In the current PSA era, though, most
men who are undergoing prostate biopsy do not have palpable abnormalities or hypoechoic
lesions This has lead investigators to question the sampling adequacy of the standard
sextant prostate biopsy template and to propose alternate extended pattern biopsy
schemes to improve prostate cancer detection. The alternate prostate biopsy templates aim
to improve sampling of the prostate by either increasing the number of core biopsies taken
and/ or by directing the biopsies more laterally to better sample the anterior horn (Chen et
al, 1999, Naughton et al., 2000). During biopsy, the puncture path is shown on the monitor
as electric dotted line. The probe should be positioned so that the puncture path passes
through the designated area. Without moving the probe, the needle is introduced through
the needle guide and the needle tip is positioned proximal to the suspicious area. A trigger
action biopsy gun is used to obtain a core specimen in an instance once the biopsy needle in
place. The biopsies performed while the biopsy needle is directed parallel to the transducer
in the sagittal plane so the needle seen as an echogenic linear structure approaching the
suspicious area, instead of an echogenic dot in the axial plane (Lee et al., 1988).

Fig. 14. Systematic TRUS guided biopsy of the upper (A), middle (B) and lower (C) parts of
the lateral regions peripheral zone (arrowheads)

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7. Role of new ultrasound techniques in diagnosis of prostate cancer

Conventional gray-scale US has low sensitivity and specificity and is mainly used for
guiding systematic prostate biopsies. With the development of new US techniques, such as
three dimensional US color and power Doppler US, the use of US contrast agents and
elastography, the role of US for prostate cancer detection has dramatically improved.
7.1 Three dimensional (3D) US of the prostate
It gives views of the prostate in the 3 orthogonal planes; sagital, transverse and coronal and
in any other oblique planes (Fig. 15). The detection rates of prostate cancer were significantly
improved with 3D- TRUS. Also it may improve the biopsy yield by determining appropriate
sites for target and systematic biopsies (Cool et al., 2008, Shen et al., 2008). With 3D imaging,
spatial relationships much clearer, so radiologist/ urologist can better assess the extent of
disease. It may make it easier to determine whether the prostate capsule has been
penetrated to detect possible extra-capsular tumor extension which is a key factor in staging
of prostate cancer. It provides valuable information to plan for alternative therapies, like
radiotherapy of the prostate and robotic prostatectomy. The 3D images are saved and they
can be reviewed as many times as needed. Diagnosis can be achieved by retrieving the
saved images which is most convenient for the operator and patient, leading to faster
patient turnaround (Liang et al., 2010, Bax et al., 2008).

Fig. 15. 3D images of a prostate with cancer. The image has been sliced to reveal a
hypoechoic lesion in the right side of the PZ (arrowhead) proved to be a cancer
7.2 Color Doppler sonography of the prostate
Color Doppler TRUS (CD-TRUS) has been applied to evaluate the vascularity within the
prostate and the surrounding structures. Preliminary studies demonstrated increased flow
within or surrounding prostate neoplasm, whereas prostatitis and BPH showed a diffusely
abnormal flow.However, the flow of focal prostatitis was not significantly different from
cancer. By using objective measures, as resistive indices, no statistically significant
difference was found between cancer and benign conditions (Rifkin et al, 1993). CD-TRUS
may help in determining the site of biopsy. If the level of PSA is elevated with DRE normal
in one patient, the presence of hypervascular focal lesion in PZ makes the lesion the target of
the biopsy. But, if the nodule is hypovascular, we have to biopsy the anterior part of the
gland to detect carcinoma of the TZ. (Cornud et al., 1993). Early results have suggested that
up to 85% of men with prostate cancers greater than 5 mm in size have visibly increased

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flow in the area of tumor involvement. In addition, hypervascularity may be seen in patients
with more difficult to identify, isoechoic and hyperechoic lesions (Fig. 16). Unfortunately,
subsequent studies suggested that some prostate cancers are hypovascular. Many studies
prove the benefits of CD-TRUS for the evaluation of prostatic disease, especially carcinoma.
The motivation behind the application of color Doppler US is to detect tumor
neovascularity. Cancerous tissue generally grows more rapidly than normal tissue and
demonstrates increased blood flow; as compared to normal tissue and benign lesions. Color
Doppler US may demonstrate an increased number of visualized vessels, as well as an
increase in flow rate, size and irregularity of vessels within prostate cancer (Newman et al.,
1995 Littrup et al., 1995, Ismail et al., 1997)

Fig. 16. (A) TRUS shows hypoechoic areas proved to be cancer (arrows). (B) Color-Doppler
shows the same area to be of high vascularity (arrows). (C) TRUS of another patient with
prostate cancer appears as hypoechoic area (arrows). (D) The same area appears with
normal vascularity in color Doppler. (E) TRUS of a third patient with hypoechoic lesion of
prostate cancer appears as hypoechoic (arrows). (F) The same lesion appears of low
vascularity in color Doppler
7.3 Power Doppler sonography of the prostate
Power Doppler US is an amplitude-based technique for the detection of flow. It is more
sensitive to slow flow and is less angle-dependent than color Doppler US. This technique
has been less commonly applied to the assessment of prostate tumor vascularity, and there
are few papers addressing its use. Some studies showed that prostate cancer are
hypervascular by power Doppler (Fig. 17) so it may be useful in detection of prostate cancer
(Inahara et al., 2004). Halpern et al assessed the value of gray-scale, color and power
Doppler US for detection of prostatic cancer. They investigated 251 patients prior to biopsy
and they hey concluded that power Doppler may be useful for targeted biopsies when the
number of biopsy passes must be limited but that there is no substantial advantage of power
Doppler over color Doppler (Halpern et al., 2000).

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Fig. 17. (A) TRUS show a hypoechoic lesion in the right posterolateral aspect of the
peripheral zone proved to be cancer. (B) The same area is hypervascular in power Doppler
(C) TRUS in another patient with prostate cancer shows no evident focal lesion in grey scale
US. (D) Power Doppler of the same patient show focal area of increased vascularity in the
right side of the peripheral zone proved to be carcinoma by targeted biopsy
7.4 Contrast enhanced ultrasound imaging
Recently developed US contrast agents can improve the detection of low-volume blood flow
by increasing the signal-to-noise ratio. Unlike radiographic contrast media, which diffuse
into the tissue and may obscure smaller vessels, microbubble echo-enhancing agents are
confined to the vascular lumen, where they persist until they dissolve. They have two
important acoustic properties, first, they are many times more reflective than blood, thus
improving flow detection. Second, their vibrations generate higher harmonics to a much
greater degree than surrounding tissues (Forsberg et al, 1998). Bree RL and De Dreu SE
showed that contrast enhanced color Doppler US had a sensitivity of 53%, specificity of 72%,
and a positive predictive value of 70% in distinguishing prostate cancer from benign lesions
in 72 patients identified by PSA screening (Bree RL & DeDreeu SE,1998). Most investigators
showed increased sensitivity in detection of prostate cancer after the use of contrast
enhanced US (Fig. 20). In the study of Bogers et al, they showed that sensitivity of enhanced
images was 85% (specificity 80%) compared with 38% for unenhanced images (specificity
80%) and 77% for conventional gray-scale transrectal US (specificity 60%) (Bogers et al.,
1999). Frauscher et al reported the value of contrast enhanced color Doppler in a prospective
study in 90, and 230 male screening volunteers (Frauscher et al., 2001, 2002). They found that
targeted biopsies based on contrast enhanced color Doppler detected as many cancers as

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systematic biopsies, with fewer than half the number of biopsy cores. Halpern et al, in their
prospective study of contrast-enhanced transrectal US in 60 patients who underwent sextant
biopsy of the prostate concluded that the sensitivity increased from 38% at baseline to 65%
after contrast injection (Fig. 18). However there was no significant change of specificity
between baseline study (83%) and during contrast aging (80%) in the same study (Halpern
et al., 2001).

Fig. 18. (A) TRUS of a patient with prostate cancer show no evident focal lesions in grey
scale US. (B) Contrast enhanced TRUS shows focal area of hypervascularity in the left side of
the peripheral zone (arrowheads) proved to be carcinoma by targeted biopsy
7.5 Elastography of the prostate
Elastography or strain imaging was first described in 1991 (Ophir et al., 1991). This
technique can be used to detect degree of stiffness of the tissues. In a pilot study done by
Klauser et al, patients with clinically localized prostate cancer who underwent radical
prostatectomy were examined prospectively. They found that elastography detected 28 of 32
cancer foci (sensitivity 88%) and they concluded that elastography is a sensitive new
imaging modality for the detection of prostate cancer (Klauser et al., 2003). Konig et al.
evaluated elastography for biopsy guidance for prostate cancer detection in 404 men
underwent systematic sextant biopsy. They found that in 127 of the cancer proved 151 cases
(84.1%), prostate cancer was detected using elastography as an additional diagnostic feature.
They concluded that it is possible to detect prostate cancer with a high degree of sensitivity
using real-time elastography in conjunction with conventional diagnostic methods for
guided prostate biopsies (Konig et al., 2005). Supersonic shear imaging (SSI) is a new USbased technique for real-time visualization of soft tissue elastographic properties. Using
ultrasonic focused beams, it is possible to remotely generate mechanical vibration sources
radiating low-frequency, shear waves inside tissues (Bercoff et al., 2004). Athanasiou et al
studied quantitative ultrasonographic elastography of breast lesions in 46 women. They
concluded that SSI provides quantitative elasticity measurements, thus adding
complementary information that potentially could help in breast lesion characterization
with B-mode US (Athanasiou et al., 2010). Recently a preliminary study by Correas et al
done to evaluated the feasibility of TRUS quantitative Shear Wave Elastography (SWE) for
prostate cancer evaluation in 21 patients presenting with increased PSA values (Fig. 19).
Elasticity measurements and ratios between nodules and adjacent parenchyma were

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calculated. They found that signals were obtained in both the peripheral and the transition
zones with good correlation to anatomical areas, macro-calcifications exhibited very high
stiffness values and prostate cancer nodules exhibited a high stiffness than the adjacent
peripheral gland. Also they noticed that peripheral adenomatous hyperplasia and focal
prostatitis exhibited a significantly lower stiffness. They concluded that TRUS quantitative
SWE is a feasible technique for prostate cancer evaluation. It provides additional
information about stiffness of nodules localized in the peripheral zone (Correas et al., 2011).
These preliminary results are encouraging but a larger multicentric evaluation remains
necessary.

Fig. 19. (A) TRUS of a normal homogeneous PZ. (B).TRUS-SWE shows homogeneous blue
coding of PZ (arrow) indicating its soft texture. (B) TRUS of another patient shows a
hypoechoic area in left PZ proved to be carcinoma (atypical pattern). (D) TRUS-SWE of the
same patient shows the focal area has blue coding (arrow) indicating its soft texture. (E)
TRUS of another patient with a hypoechoic nodule in the left PZ proved to be carcinoma
(arrow). (F) TRUS-SWE of the same patient shows a strong increase in stiffness values of the
focal area (red) with a ratio of 2.8 compared to the surrounding PZ (typical pattern)
(adapted from Correas et al 2011)

8. Role of ultrasound in prostate cancer treatment

Recent interest in focal therapy for localized prostate cancer has been driven by downward
stage migration, improved biopsy and imaging techniques. Several techniques have
potential for focal ablation of prostate cancer.
8.1 TRUS-guided cryotherapy for prostate cancer
Cryotherapy is tissue ablation by local induction of extremely cold temperatures. The first
use cryoablation in urological disorders started in the 1960s for management of benign
prostatic hyperplastic tissue (Gonder et al., 1966). This was followed shortly thereafter by
the treatment of prostate cancer via an open perineal approach (Fig. 20). The major
impediment to early acceptance of the modality, however, was the inability to accurately

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monitor cryoprobe placement and ice-ball formation. Major advances in the past 20 years,
which have reinvigorated investigation into the use of cryotherapy for prostate cancer, have
included the use of TRUS monitoring of probe placement and freezing (Onil et al,1993). A
significant recent development was the introduction of cryotherapy probes that use argon
gas rather than liquid nitrogen (De La Taille et al., 2000). Outcomes have now been reported
as late as 7 years following treatment of prostate cancer and seem to compare favorably with
contemporary series of patients who receive radiation therapy (Bahn et al., 2002 ). Marberger
et al reported that cryotherapy has been used for some time as a form of first-line therapy
for complete ablation of the prostate or and as a second-line therapy for local recurrence
after radiotherapy (Marberger et al., 2008).

Fig. 20. (A) TRUS of the prostate illustrating placement of the cryoprobes and urethralwarming catheter. (B) TRUS of the prostate during cryoablation showing the ice ball,
growing posteriorly, is echodense and casts a dark acoustic shadow. (C) The ice ball extends
posteriorly to include the whole prostate tissue. Transrectal sonogram of the prostate
illustrating placement of the cryoprobes and urethral-warming catheter
8.2 High-intensity focused ultrasound (HIFU)
HIFU is one of the newer methods that have been developed to treat early stage prostate
cancers. High energy is delivered to the affected area by ultrasound, this result in the
targeted cancerous cells heating up and being destroyed. Using extracorporeal HIFU,
temperatures of greater than 60C can be achieved in the target tissue. The prostate can be
easily treated with this modality via a transrectal probe. Gelet et al pioneered the use of
transrectal HIFU in the treatment of localized prostate cancer. Prostates smaller than 40 mL
or those with an anteroposterior diameter of less than 5 cm are best suited for this treatment.
During the procedure, the whole gland is treated. They reported that 78% of low-risk
patients were disease-free and had negative biopsy results at an actuarial 5-year follow-up
(Gelet et al., 2004). Some of the advantages of HIFU are that it is able to be repeated if cancer
reappears; it can destroy cancer in targeted areas of the prostate without destroying other
areas of the prostate; and it can be given to patients who may not be able to take other forms
of prostate treatment such as brachytherapy. Marberger et al reported that HIFU has been
used widely in Europe for complete ablation of the prostate, especially in elderly men who
are unwilling or unable to undergo radical therapy. For low- or intermediate-risk cancer, the
short- and intermediate-term results have been acceptable. Focal use of HIFU should reduce
the adverse sexual and urinary side effects of whole gland ablation (Marberger et al., 2008).

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8.3 Vascular-targeted photodynamic therapy (VTFT)

VTFP is a minimally invasive ablative treatment for localized prostate cancer and may
represent a preferred option for men with low-risk disease who want to balance the risks
and benefits of treatment. (Lepor, 2008). VTPT has been used for whole gland ablation of
locally recurrent cancer after radiotherapy and for focal ablation of previously untreated
cancer. In combination with a new, systemically administered photodynamic agent, laser
light is delivered through fibers introduced into the prostate under TRUS. This technique
does not heat the prostate but destroys the endothelial cells and cancer by activating the
photodynamic agent. Damage to surrounding structures appears to be limited and can be
controlled by the duration and intensity of the light. (Marberger et al., 2008).
8.4 TRUS-guided prostate brachytherapy
Brachytherapy is an effective treatment for localized prostate cancer with high patient
tolerability and acceptable morbidity outcome data. It delivers a high dose of radiation to a
small target volume of tissue, minimizing radiation side-effects to adjacent structures.
Brachytherapy is an alternative to radical surgery and external beam radiotherapy and can
be delivered in two different ways: permanent seed implants using iodine or palladium seeds
or using temporary removable implants with iridium wires. TRUS is essential for accurate
imaging guidance to place the radioactive sources into the prostate (Fig. 21). Prostate
brachytherapy data has now matured as a treatment with consistent results reported from
major centers in the US and Europe (Henry et al., 2010, Battermann et al., 2008).

Fig. 21. Prostate brachytherapy. (A) Transrectal ultrasound set-up: transverse image of the
prostate with 5mm template overlay. (B) Transverse image of the prostate after seed implant
(echogenic areas)

9. Conclusion
One of the major advances that have greatly improved our understanding of prostatic
diseases is the development of sonography especially TRUS. It is considered the first
imaging modality in diagnosis of prostate diseases. Improvement of the application of the
new advances in US for the detection and clinical staging of prostate cancer is promising.
TRUS-guided procedures are now widely used in diagnosis and treatment of prostate
cancer. Radiologists and urologists should be well trained in the application of these new US
techniques and should therefore play an important role in the management of prostate
cancer in the future.

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Sonography

Edited by Dr. Kerry Thoirs

ISBN 978-953-307-947-9
Hard cover, 346 pages
Publisher InTech

Published online 03, February, 2012

Published in print edition February, 2012

Medical sonography is a medical imaging modality used across many medical disciplines. Its use is growing,
probably due to its relative low cost and easy accessibility. There are now many high quality ultrasound
imaging systems available that are easily transportable, making it a diagnostic tool amenable for bedside and
office scanning. This book includes applications of sonography that can be used across a number of medical
disciplines including radiology, thoracic medicine, urology, rheumatology, obstetrics and fetal medicine and
neurology. The book revisits established applications in medical sonography such as biliary, testicular and
breast sonography and sonography in early pregnancy, and also outlines some interesting new and advanced
applications of sonography.

How to reference

In order to correctly reference this scholarly work, feel free to copy and paste the following:
Ragab Hani Donkol and Ahmad Al Nammi (2012). Prostate, Sonography, Dr. Kerry Thoirs (Ed.), ISBN: 978953-307-947-9, InTech, Available from: http://www.intechopen.com/books/sonography/prostate

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