Professional Documents
Culture Documents
S INCE its clinical application in In 1988, with 2 years experience performed, and readily accepted by
1971 by Watanabe (1), transrectal with 7-MHz scanners, the appear- patients.
ultrasound (TRUS) has now devel- ance of prostate cancer is generally By applying McNeal’s concept of
oped into a sophisticated technology. accepted as hypoechoic (9-11). Can- zonal anatomy, we now understand
Its widespread acceptance is reflected cers may appear isoechoic if they are areas of anatomic weakness through
in increased numbers of scientific smaller than the size allowed by re- which cancer may escape the con-
publications on prostate imaging in solving capabilities of the scanner, or fines of the prostate. Strategic US-
the current literature. if the tumor involves the entire pros- guided transrectal biopsy accurately
Early in the history of TRUS, bi- tate, thus replacing any residual nor- samples these areas. The role of biop-
stable 3-MHz transverse images pro- ma! tissue. In our recent screening sy has been extended from its use in
vided information about prostate size program, 9% (two of 22) of the can- the diagnosis of prostate cancer to in-
and shape (2). In the late 1970s and cers were initially overlooked with dude evaluation of tumor extension
early 1980s, gray-scale longitudinal TRUS and diagnosed by means of for staging.
and transverse scanners were intro- digital rectal examination (ORE) (12). The results reported in the litera-
duced (3). Visualization of the inter- We have thus witnessed marked ture have been confusing due to non-
nal architecture of the prostate was technical improvements and changes uniformity in equipment and the cri-
then possible, and two zones were in image interpretation. The fact that teria applied for cancer echogenicity.
identified: the internal and the exter- the appearance of prostate cancer was Still in 1988, data are published in
nal gland. At that time, the majority thought to be hyperechoic and then which conclusions are based on the
of investigators believed cancers hypoechoic did little to lend credibil- use of uniplanar 4.0-MHz equipment
were hyperechoic (4-6). ity to TRUS. However, implementa- and lack of a criterion for cancer
In 1985, studies were performed tion of TRUS in the diagnosis of echogenicity (19). A recent literature
with 5.0 MHz scanning in both trans- prostate cancer is now widespread. review has documented this confu-
verse and longitudinal planes. The An evolution in biopsy technique sion (20).
hyperechoic nature of prostate cancer has paralleled the improvements in Our current concepts of the clinical
was then challenged (7). US imaging. Transperineal biopsies significance of the zonal anatomy of
In 1986, 7.0-MHz scanning was in- guided by transverse imaging in 1981 the prostate and the importance of
troduced. The improvement in reso- (13), and longitudinal imaging in strategic US-guided biopsy for diag-
lution allowed visualization of the 1983 (14), are still performed. More nosis and staging of prostate cancer
infrastructure of the prostate corre- recently, 7.0-MHz longitudinal scan- are described herein.
sponding to McNeal’s 1981 concept ners with transrectal biopsy capabili-
of zonal anatomy (8). ties have caused a trend toward biop-
PROSTATE ANATOMY
sy by the transrectal route (11,15,16).
Ease of biopsy is important for le- Current textbooks still describe
Index terms: Prostate, biopsy, 844.126 Pros-
#{149}
the Department of Clinical Research and Clini- digital rectal examination, PZ = peripheral
of smaller lesions as well as of multi-
cal Research Committee of St Joseph Mercy zone, TRUS = transrectal ultrasound, TURP =
Hospital. Address reprint requests to F.L. ple areas in the gland (18). Transrec- transurethral resection of the prostate, TZ =
609
TRANSON ZONE
a.
b. C. d.
Figure 1. Transition zone (TZ). (a) Graphic depiction of the TZ (blue) viewed from the top. (b) Graphic depiction of the TZ (blue) viewed
from the side. (c) Transverse histologic whole mount of TZ tissue. (d) Axial scan of TZ. The proximal urethra (*) separates the bilateral TZ.
The TZ is separated from the peripheral zone (PZ) by the surgical capsule (arrows). The verumontanum (*) gives an Eiffel Tower configura-
tion on TRUS. The urethra subtends an angle of 350 at the level of the verumontanum.
CENTRAL ZONE
a.
b. c. d.
Figure 2. Central zone (CZ): (a) Graphic depiction of the CZ (orange), viewed from the top. (b) Graphic depiction of the CZ (orange),
viewed from the side. (c) Histologic whole mount of CZ tissue. (d) Sagittal scan of CZ. The confluens of the seminal vesicle (SV) and the vas
deferens (VD) form a beak configuration (arrowheads), which continues as the ejaculatory duct (arrows). The loose connective tissue of the
extraprostatic space (x) invaginates with the SV beak, forming the invaginated extraprostatic space, which follows the ejaculatory duct to the
verumontanum (*). B = urinary bladder, * urethra, PZ = peripheral zone, R = rectum, DE = Denonvilliers fascia, AFS = anterior fibro-
muscular stroma, PS = preprostatic sphincter.
dular zones-transition, central, and The proximal urethra is surround- dular tissue. It is composed of smooth
peripheral zones-and one nonglan- ed by periurethral glandular tissue muscle and extends from the bladder
dular region-anterior fibromuscular whose ducts open directly into the neck to verumontanum.
stroma. The urethra, its associated ureteral lumen. Prostatic calculi may Varying amounts of striated mus-
sphincteric complexes, and the ejacu- form within these glands and appear cle are present around the distal ure-
latory ducts pass through these as echogenic foci on TRUS scans (24). thra and blend with the external
zones. These calculi are thought to be sec- sphincter at the apex of the prostate.
In its passage through the prostate, ondary to reflux of urine into the
the urethra is divided into proximal ducts (exogenous), differing from the
Transition Zone
(from bladder neck to verumon- corpora amylacea that arise from the
tanum) and distal (from verumon- prostatic glands (endogenous). The The transition zone (TZ) (Fig 1),
tanum to external sphincter). The internal or preprostatic sphincter is prior to development of benign pros-
proximal and distal urethra form an situated around this complex of prox- tatic hyperplasia, constitutes approxi-
angle of 35#{176}at the verumontanum. imal urethra and periurethral glan- mately 5% of prostatic glandular tis-
610 Radiology
#{149} March 1989
TRAPEZOID AREA
a. b. C.
d.
Figure 4. Graphic depiction of zonal anatomy of the prostate gland. Blue = TZ, orange =
612 Radiology
#{149} March 1989
weakness (Fig 6). This po- the surgical capsule,
BIPLANE _________
which separates it from
tential pathway for cancer
spread, the invaginated
#{149}
Sector-Sector \I // the TZ. The TZ appears to
extraprostatic space, ex- be relatively resistant to
tends the length of the cancer invasion from the
ejaculatory ducts to the PZ unless a cancer is large
verumontanum. There is (28).
no tissue barrier between Cancer frequently in-
the invaginated extrapros- BIPLANE _____ volves the apex of the
tatic space and the adja- #{149}
Sector-Linear Jj prostate, where prostate
cent CZ, allowing cancer capsule is thin or absent,
easy access to this path- thus allowing ready ac-
way. Thus, tumor spread cess to the trapezoid area
can readily extend from (25,31) (Fig 7).
the base to the apex of the
prostate gland. When ejac- MULTIPLANE ________
ulatory ducts become en- #{149}
Rotating Sector
IMAGING
veloped by cancer, a “ha- #{149}
Symmetncal TECHNIQUES
lo” sign may be seen on The capability to obtain
axial images. Partial ob- images in transverse as
struction can occur with well as sagittal or parasag-
dilatation of the ipsilater- ittal planes must be avail-
al seminal vesicle. MULTIPLANE able for optimal evalua-
Currently, our US crite- tion of the prostate.
na for seminal vesicle #{149}
Moveable
Though many transducer
and/or ejaculatory duct designs are currently
involvement are (a) a “ha- available (Fig 8), the most
lo” about the ejaculatory
effective design is an
duct produced by sur- “end-viewing” transducer
rounding tumor, (b) oblit- in which scan planes are
eration or displacement of
MULTIPLANE
directly centered along
the beak of seminal vesi- the long axis of the trans-
cle by cancer, (c) cancer ducer. Since the probe
directly extending into a acts as a direct extension
seminal vesicle (31), and/ of the hand, simple ma-
or (d) an extraprostatic neuvering or rotation al-
mass at the entrance of lows instantaneous multi-
Figure 8. Multiplanar/biplanar probes: Biplane sector-sector probe:
the seminal vesicle obli- directional imaging. Rap-
The two sectors are at right angles to each other. The planes over-
terating the seminal vesi- lap in a distal part of the image. Therefore most lesions will have id evaluation of the three
cle/prostate angle. to be relocated when the scan plane is changed. Biopsy is limited dimensions of any suspi-
Microscopic extension to the transperineal route. Biplane sector-linear probe: The linear cious hypoechoic lesion is
of cancer into either the probe is used for longitudinal scanning, and the sector, which
thus possible. Scan planes
seminal vesicles, or along may be a curved array, is used for transverse imaging. There is no
overlap between planes. All lesions must be relocated when the in transverse projections
the invaginated extrapros- are oblique to the true
scan plane is changed. Biopsy is limited to the transperineal route.
tatic space, cannot be Multiplane rotating sector probe with symmetrical rotating axis: All transverse planes, wheth-
demonstrated with TRUS. planes between longitudinal and transverse can be obtained. The er an axial or end-viewing
If a lesion is adjacent to rotation axis is in the center of the image. Any structure on the transducer is used (Fig 9).
the ejaculatory ducts, sem- center axis of the image will stay in the image as the scan plane is In our practice, this end-
inal vesicles, or the medi- changed. Biopsy is limited to the transperineal route. Multiplane
nonmovable sector probe: The scan plane is changed by rotating the viewing probe has proved
al base of the prostate, a highly effective for both
housing of the transducer. All planes between longitudinal and
staging biopsy of the ap-
“transverse” are obtained. The transverse planes sweep from co- diagnosis and biopsy of
propriate areas of poten- ronal to horizontal by tilting the transducer. Any structure on the the prostate.
tial spread must be per- center axis of the image will stay in the image as the scan plane is
formed. changed with rotation. Transrectal biopsy can be performed. Mu!-
tiplane rotating sector probe with asymmetrical rotating axis: Because BIOPSY
the rotation axis is off center, the 40#{176} transverse image changes to
a longitudinal image demonstrating the tissues in front of the The presence of a hypo-
Peripheral Zone
transducer. Any structure on the rotation axis will remain in the echoic lesion only sug-
Seventy percent of image as the scan plane is changed. Both transrectal and transper- gests cancer, which must
prostate cancers originate meal biopsies are possible. be proved by biopsy. With
in the PZ (25). These can- the end-viewing probe,
cers, which may be multi- transrectal biopsies can be
focal (31), are usually located close to from the CZ is easily traversed by performed anywhere in the prostate,
or in direct contact with the prostate cancer. Thus, a PZ cancer can directly in any projection (Fig 10).
capsule. Cancer spreads down these extend into the CZ and spread to The main role for TRUS-guided bi-
paths of least resistance (32): (a) into ejaculatory ducts and/or seminal yes- opsies is to obtain tissue for histolog-
the subcapsular space, and/or (b) ides via the invaginated extraprosta- ic diagnoses. Several cores are neces-
along the prostatic acini and ducts. tic space. sary to enable accurate prediction of
The interface separating the PZ Medially, the PZ is bordered by histologic grade and evaluation of
10.
possible extraprostatic extension. THE ROLE OF TRUS than DRE. Since TRUS can also offer
Since we can now visualize the inter- information regarding tumor size
nal anatomy of the prostate, we can An imaging procedure for evaluat- and extent, we recommend that
predict and prove extraprostatic ex- ing anatomic details in the prostate TRUS-guided biopsy be performed
tension by using strategic TRUS- provides valuable information in the first on all palpable lesions. Studies
guided biopsy of known sites of ana- study of prostate cancer. have shown that up to 50% of nega-
tomic weakness: (a) the seminal vesi- In a screening setting, the presence tive biopsies guided by palpation
cle beak, (b) the invaginated of a hypoechoic lesion proved to be have been subsequently proved posi-
extraprostatic space, which follows twice as sensitive as a palpable ab- tive for cancer with TRUS-guided bi-
the ejaculatory ducts to the verumon- normality in predicting the presence opsy (18,33). Should a TRUS-guided
tanum, and (c) the trapezoid area. of cancer (12). In this study, for every biopsy of a palpable lesion not dis-
The automatic Biopty system (Bard two cancers detected with TRUS, one close cancer, a palpation-guided bi-
Urological Division, Covington, Ga) is cancer was detected with DRE. opsy must be performed.
superior to any other method we have In our clinical setting, where a hy- The role of TRUS in staging is to
tried for obtaining histologic speci- poechoic lesion was the criterion for obtain tissue from areas where micro-
mens via the transrectal route (Fig 11). biopsy, 41% proved to be cancer (15). scopic extracapsular extension is like-
In more than 1,000 biopsies, we have Sixty-eight percent of these cancers ly to be present. Biopsy may provide
never obtained insufficient tissue. In were palpable. Therefore, for every histologic confirmation.
the past, using the transperineal route four cancers detected with TRUS, When TURP discloses unsuspected
for biopsy we experienced insuffi- three cancers were detected with cancer and a staging TURP is indicat-
cient tissue cores and crush artifacts DRE. ed, TRUS may be an alternative.
with the 19-gauge Sure-Cut (Sure-Cut In another clinical setting, where a TRUS-guided biopsy of suspected re-
biopsy needle, 230 mm; Meadox Sur- palpable lesion was the criterion for sidual tumor is less expensive and
gimed, Oakland, NJ) and 14-gauge biopsy, 14 cancers were diagnosed less traumatic than repeat TURP.
Tru-Cut needles (Tru-Cut biopsy nee- (19). Transperineal biopsies were
dle, 11.4 cm; Travenol Laboratories, guided by palpation and by TRUS. THE ROLE OF TRUS IN
Deerfield, Ill) (17,18). DRE-guided biopsy results were posi- SCREENING
Strategic TRUS-guided biopsy al- tive for cancer in 13 cases, and TRUS
lows for more accurate staging when in 12. Therefore, though the numbers The role of US in detecting non-
a diagnosis of prostate cancer has were small and the US equipment palpable cancer is controversial.
been established (16). We are cur- was substandard, detection rates for Nonpalpable cancers cannot be
rently conducting an ongoing pro- TRUS and DRE were nearly equal. found without screening. It is accept-
spective study using strategic TRUS- Thus, in any diagnostic situation ed that palpable cancers are clinically
guided biopsy. TRUS is equal to or more sensitive relevant. The clinical significance of
614 Radiology
#{149}
March 1989
nonpalpable cancers found by TRUS die of prostate cancer in 1988 (37). 15. Lee F, Torp-Pedersen S. Littrup PJ. Hypo-
echoic lesions of the prostate: clinical rele-
has yet to be determined. Autopsy Because prostate cancer is the second vance of tumor size, digital rectal examina-
and prostatectomy data will provide leading cause of death from cancer in tion, and prostate-specific antigen. Radiology
1989; 170:29-32.
information about this issue. American men, along with colorectal 16. Stamey TA. Ultrasound-guided Biopty cores:
There is a good correlation be- cancer, we must utilize diagnostic a revolution for the urologist. Presented in
Transrectal Ultrasound of the Prostate: A
tween the volume of cancer and the modalities that enable early detec- Practical Course for Urologists. Stanford Uni-
malignancy potential. In an analysis tion. We support the use of TRUS in versity School of Medicine Postgraduate
Medical Education course, Palo Alto, Califor-
of 100 autopsy specimens, McNeal the early detection of prostate cancer. nia, January 1988.
showed that prostate cancers reach- 17. Lee F, Littrup PJ, McLeary RD. et al. Needle
aspiration and core biopsy of prostate cancer:
ing a size of 1.0 cm3 were clinically comparative evaluation with biplanar trans-
significant (due to capsular invasion SUMMARY rectal US guidance. Radiology 1987; 163:515-
520.
and/or extraprostatic tumor exten- Indications for TRUS are: (a) for di- 18. Torp-Pedersen ST. Lee F, Littrup PJ, et al.
sion) (34). He also showed that the agnosis of nonpalpable cancer, or de-
Transrectal biopsy of the prostate guided by
transrectal ultrasound: experience with longi-
majority of tumors exceeding 3.0 cm3 tection of cancer with greater accura- tudinal and multiplane scanning. Radiology
were no longer confined within the cy than is possible at present; (b) for
1988 (in press).
19. Resnick MI. Transrectal ultrasound guided
prostate. Using this correlation be- guidance of transrectal biopsies of versus digitally directed prostatic biopsy: a
tween tumor volume and malignancy hypoechoic lesions for histologic
comparative study. J Urol 1988; 139:754-756.
20. Cole HM, ed. Diagnostic and therapeutic
potential, we may select those pros- confirmation of cancer; (c) for guid- technology assessment (DATTA): transrectal
tate cancers we wish to diagnose. ance of staging biopsies to ensure di-
ultrasonography in prostate cancer. JAMA
1988; 259:2757-2759.
If in a screening setting we limit agnoses of extraprostatic extension; 21. McNeal JE. Regional morphology and pa-
diagnoses to cancers >0.5 cm3, we thology of the prostate. Am J Clin Pathol
and (d) for staging previously diag- 1968; 49:347-357.
will diagnose 35% of the cancers. nosed prostate cancer. U 22. Blacklock NJ, Boushill K. The zonal anatomy
Prevalence in McNeal’s study was of the prostate in man and in the rhesus mon-
key. (Macaca mulatta). Urol Res 1977; 5:163-
23% (100 of 436). The prevalence 167.
then for those cancers we wish to di- Acknowledgments: The authors wish to ex- 23. Salander H, Johansson 5, Tisell LE. The his-
press their gratitude to Robin Hite, medical il- tology of the dorsal, lateral, and medial pros-
agnose (>0.5 cm3) is 8% (35% of 23%). lustrator; Anne Mitchell, literary consultant; tatic lobes in man. Invest Urol 1981; 18:479-
This prevalence is probably a maxi- 483.
and Michael Wilson, ultrasound technician.
24. Orland SM, Hanno PM, Wein AJ. Prostatitis,
mum value, since it is derived from prostatosis, and prostatodynia. Urology 1985;
an autopsy series and not from 5:439-459.
References 25. McNeal JE. Normal anatomy of the prostate
healthy men without symptoms. gland: axial and s.agittal planes. Presented in
1. Watanabe H, Kaiho H, Tanaka M, Terasawa Y. Transrectal Ultrasound of the Prostate: A
Screening for prostate cancer is
Diagnostic application of ultrasonotomo- Practical Course for Urologists. Stanford Uni-
highly misunderstood. A 30% preva- graphy to the prostate. Invest Urol 1971; versity School of Medicine Postgraduate
lence of prostate cancer at autopsies 8:548-549. Medical Education course, Palo Alto, Califor-
2. King WW, Wilkiemeyer RM, Boyce WH, Mc- nia, January 1988.
does not mean that 30% of prostate Kinney WM. Current status of prostatic 26. Isaacs JT. Prostatic structure and function in
cancers should be diagnosed in the echography. JAMA 1973; 226:444-447. relation to the etiology of prostatic cancer.
3. Harada K, Igari D, Tanahashi Y. Gray scale Prostate 1983; 4:351-366.
general population (35). transrectal ultasonography of the prostate. 27. Whitmore WF Jr. The rationale and results
Applying population and cancer Clin Ultrasound 1979; 7:45-49. of ablative surgery for prostatic cancer. Can-
4. Resnick MI, Willard JW, Boyce W. Recent cer 1963; 1119-1132.
statistics, Scardino developed a meth- progress in ultrasonography of the bladder 28. McNeal JE, Price HM, Redwine EA, Freiha FS,
od to define screening prevalence and prostate. J Urol 1977; 117:444-445. Stamey TA. Stage A versus stage B adenocar-
5. Peeling WB, Griffiths GJ, Evans KT, Roberts cinoma of the prostate: morphological com-
(36): EE. Diagnosis and staging of prostatic cancer parison and biological significance. J Urol
by transrectal ultrasonography: a preliminary 1988; 139:61-65.
(a) If the autopsy prevalence for study. Br J Urol 1979; 51:565-569. 29. Anderson WAD, Kissane JM. Pathology. Vol
6. Rifkin MD, Kurtz AB, Choi HY, Goldberg BB. 1. St Louis: Mosby, 1977; 999-1007.
prostate cancer is 30% of men Endoscopic ultrasonic evaluation of the pros- 30. Lee F. Transrectal ultrasound of pre-TUR
over 50 years of age, and there tate using a transrectal probe: prospective and post-TUR stage A prostate cancer. Pre-
evaluation and acoustic characterization. Ra- sented at the Third International Symposium
are 27,310,000 men over the age diology 1983; 149:265-271. on Transrectal Ultrasound in the Diagnosis
of 50 in the United States, then 7. Lee F, Gray JM, McLeary RD. et at. Transrec- and Management of Prostate Cancer, Chica-
tal ultrasound in the diagnosis of prostate go, September 1988.
there are 8,193,000 cancers in the cancer: location, echogenicity, histopatholo- 31. Byar DP, Mostofi FK. Carcinoma of the pros-
men over 50 in the United States gy, and staging. Prostate 1985; 7:117-129. tate: prognostic evaluation of certain patho-
8. McNeal JE. The zonal anatomy of the pros- logic features in 208 radical prostatectornies
(30% of 27,310,000). tate. Prostate 1981; 2:35-49. examined by the step-section technique. Can-
(b) If a man over 50 years has a risk 9. Hodge K. In vitro ultrasounds after radical cer 1972, 30:5-13.
prostatectomy. Presented in Transrectal UI- 32. McNeal JE. Origin and development of carci-
of 0.35% for having prostate can- trasound of the Prostate: A Practical Course noma in the prostate. Cancer 1969; 23:24-34.
cer diagnosed per year (96,000 of for Urologists. Stanford University School of 33. McHugh TA. The value of transrectal ultra-
Medicine Postgraduate Medical Education sound for the urologist. Presented at the Sec-
27,310,000), and the average course, Palo Alto, California, January 1988. ond International Symposium on Transrectal
American man over 50 years of 10. Clements R, Griffiths GJ, Peeling WB, Roberts Ultrasound in the Diagnosis and Manage-
EE, Evans KT. How accurate is the index fin- ment of Prostate Cancer, Detroit, September
age is 64 years old and has a life ger? a comparison of digital and ultrasound 1987.
expectancy of 15 years, then the examination of the prostatic nodule. Clin Rad 34. McNeal JE, Kindrachuk RA, Freiha FS, et al.
1988; 39:87-89. Patterns of progression in prostate cancer.
risk for the average man over 50 11. Cooner WH, Mosley BR, Rutherford L Jr. et Lancet 1986; 1:60-63.
for development of prostate can- al. Clinical application of transrectal ultraso- 35. Franks LM. Latent carcinoma of the prostate.
nography and prostate specific antigen in the Pathol Bacteriol 1954; 68:603-616.
cer in his lifetime is 5.3% (15 X search for prostate cancer. J Urol 1988; 36. Scardino PT. Pathology, staging, and thera-
0.35). 139:758-761. peutic approaches to prostate carcinoma. Pre-
12. Lee F, Littrup PJ, Torp-Pedersen ST, et al. sented at a Special Focus Session of the 73d
(c) Ideally, if all men over 50 years Prostate cancer: comparison of transrectal US Scientific Assembly and Annual Meeting of
of age were screened, 5.3% will and digital rectal examination for screening. the Radiological Society of North America,
Radiology 1988; 168:389-394. Chicago, November 29-December 4, 1987.
be diagnosed with prostate can- 13. Holm HH, Gammelgaard J. Ultrasonically 37. Silverberg E, Lubera JA. Cancer statistics,
cer. guided precise needle placement in the pros-
tate and the seminal vesicles. J Urol 1981; 1988. CA 1988; 38:5-22.
125:385.
Ninety-six thousand new cases of 14. Fornage BD, Touche DH, Deglaire M, Faroux
prostate cancer are diagnosed each MC, Simatos A. Real-time ultrasound-guid-
ed prostatic biopsy using a new transrectal
year. An estimated 28,000 men will linear-array probe. Radiology 1983; 146:547-
548.