Abstract
The visceral organs of the male pelvis have complex anatomic relationships with the surrounding extraperitoneal spaces, supplying arteries and adjacent pelvic musculature. Since various neoplastic, vascular, and traumatic pathologies can often involve multiple organs and spread into adjacent pelvic spaces, a keen understanding of this intricate anatomy can help radiologists to accurately characterize findings and improve recognition of the routes in which these conditions can spread. The purpose of this review is to examine the relationships between the anatomic compartments of the pelvic extraperitoneal space, summarize the pelvic arterial anatomy, and identify the pelvic muscles that support normal genitourinary function.
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Introduction
The use of cross-sectional modalities such as computer tomography (CT) and magnetic resonance imaging (MRI) in evaluating the male pelvis has become commonplace. Radiologists should have keen understanding of the fascial layers lining the muscles and visceral organs of the male pelvis and the extraperitoneal compartments that these layers form. The communication between these spaces dictates the spread and containment of different neoplastic and traumatic pathologies. Other common conditions in the male pelvis such as high-flow priapism and benign prostatic hyperplasia have a vasculogenic origin and treatment. Though the main arterial supply for several of the organs in the male pelvis are diminutive and difficult to visualize on cross-sectional imaging, radiologists should have a basic understanding of the key pelvic arterial branches arising from the internal iliac artery. The purpose of this review is to examine the relationships between the anatomic compartments of the pelvic extraperitoneal space, summarize the pelvic arterial anatomy, and identify the pelvic muscles that support normal genitourinary function.
Extraperitoneal pelvic spaces
The pelvis is primarily located within the extraperitoneal space, which is comprised of the space between the peritoneum internally and transversalis fascia externally [1,2,3,4]. The majority of the male pelvis is located within the inferior extraperitoneal space. This space consists of an anterior and a posterior compartment that is separated by the rectovesical septum, also known as the Denonvillier’s fascia [5, 6]. The anterior pelvic compartment is divided into the prevesical space and perivesical space, while the posterior compartment is divided into the perirectal space and presacral space.
Extraperitoneal anatomy
A key structure in the delineation of the anterior pelvic compartment is the umbilicovesical fascia. Located anterior to the peritoneum and posterior to the transversalis fascia, the apex of the umbilicovesical fascia is positioned at the umbilicus and creates a triangular shape as it courses inferiorly in the pelvis. The fascia envelopes the obliterated umbilical vessels, urachus/urachal remnant and bladder [7, 8]. The umbilicovesical fascia divides the anterior pelvis into the prevesical space and encases the smaller perivesical space, a small potential space that is typically imperceptible on imaging. The perivesical space is contiguous inferiorly with the prostate and seminal vesicles (Fig. 1). On cross-sectional imaging, the umbilicovesical fascia can be distinguished by indentifying the medial umbilical ligaments (obliterated umbilical arteries) and the urachal remnant, when present (Fig. 2).
The anterior boundary of the prevesical space is the transversalis fascia, which lines the inner surface of the transverse abdominal muscles. The lateral aspect is defined by the parietal pelvic fascia that covers the internal surface of the muscles of the pelvic floor. The space is bounded by the umbilicovesical fascia posteriorly and medially. Fat, loose fibrous tissue, and venous plexus occupies this space [9]. Posterior to the pubis, the space is commonly referred to as the space of Retzius.
The posterior pelvic compartment is delineated from the anterior compartment by the rectovesicular septum. The posterior compartment can be subdivided into the perirectal space anteriorly and presacral space posteriorly. The perirectal space is outlined by the rectovesical septum anteriorly, mesorectal fascia laterally and posterior pelvic fascia posteriorly [10, 11]. In addition to the rectum and adjacent adipose tissue, the space also contains rectal arteries and veins, lymphatics and perirectal lymph nodes. Details of this space are beyond the scope of this paper. The pararectal space is a potential space between the mesorectal fascia and the parietal pelvic fascia [1, 11, 12]. The presacral space is located posteriorly within the posterior pelvic compartment. It is situated in front of the sacrum and coccyx, defined anteriorly by posterior pelvic fascia and posteriorly by the parietal pelvic fascia [8, 13].
Extraperitoneal fluid collections
Hemorrhage and extraperitoneal bladder rupture are the most common etiologies of fluid accumulation in the prevesical space. On cross-sectional imaging, collections in this space are classically described as having a “molar tooth” appearance [8]. The “crown” component of the tooth is visualized when fluid resides between the transversalis fascia and the umbilicovesical fascia causing the bladder to be displaced posteriorly. The “root” components are formed when the fluid extends into the space between the umbilicovesical fascia and the parietal pelvic fascia (Fig. 3). Though the “root” portion is sometimes referred to as a paravesicular collection, it represents extension of the perivesical space [14]. Fluid in this location compresses the bladder and displaces it medially [1].
Given the narrow configuration of the umbilicovesical fascia, isolated fluid accumulation in the perivesical space is rare. Traumatic or iatrogenic injuries that involve fluid collections or extravasation into the perivesical space is most commonly found with concomitant prevesical fluid. The perivesical space above and anterior to the bladder is often spared in patients with prevesical fluid collections (Fig. 3). The adjacent prevesical fluid delineates a triangular-shaped fatty space that contains the urachus and obliterated umbilical arteries.
Communication of the extraperitoneal spaces
Although infrequently identified clinically, fluid from the prevesical space can extend into the perivesical space. This space is contiguous with the prostate and seminal vesicles along the posterior portion of the bladder, likely facilitating communication between the compartments [1]. The perivesical space is also directly contiguous with the pararectal space, a potential space. Rarely, large perivesical collections can extend into the pararectal space and subsequently into the presacral space (Fig. 4). Although there are conflicting reports in the literature [2], it is believed that the mesorectal fascia prevents the extension of perivesical fluid into the perirectal space [11, 15, 16].
The deep inguinal ring, the proximal opening of the inguinal canal, is formed by an ovoid opening of the transversalis fascia. Fluid originating in the perivesical space can extend to the scrotum via this orifice (Fig. 5).
The sheath of the femoral canal represents a short funnel-shaped extension of the extraperitoneal space into the abdominal wall [17]. The transversalis fascia forms the anterior wall of the sheath. The femoral vessels course along the lateral aspect of the canal and are directly continuous with the external iliac vessels that reside within the prevesicular space [18]. Hemorrhage in the femoral canal can extend along the sheath and communicate with the perivesical space. This finding is frequently encountered in patients that develop large hematomas following femoral arterial catheterization (Fig. 6).
Below the umbilicus, the posterior sheath of the abdominis muscle terminates at the arcuate line, a horizontal line that denotes the inferior extent of the posterior rectus sheath [19]. Likewise, the paired inferior epigastric vessels cross the transversalis fascia below the arcuate line (Fig. 7). Fluid collections may traverse between the rectus sheath inferiorly into the prevesical space at these vascular insertion sites. Larger collections may also directly penetrate through the thinned transversalis fascia inferior to the arcuate line into the prevesical space [20] (Fig. 8).
Disease processes can also extend from the perivesical space to the retroperitoneal space. The perivesical space is contiguous with the extraperitoneal fat of the anterior abdominal wall below the transversalis fascia. There is direct extension from the perivesical space to the properitoneal and retroperitoneal fat, serving as a conduit to the anterior pararenal, perirenal and posterior pararenal spaces [8] (Fig. 9). Extension of retroperitoneal fluid inferiorly into the pelvis occurs more commonly than prevesical fluid extending superiorly into the retroperitoneum. Furthermore, fluid extending from the perirenal space into the pelvis occurs more frequently than fluid originating from the pararenal spaces [21].
Pelvic arterial vasculature
Within the male pelvis, the internal iliac artery serves as the predominant vessel providing the majority of blood flow to the pelvic viscera and surrounding musculature. Many of the smaller terminal branches of the internal iliac artery are below the resolution of cross-sectional imaging. Nevertheless, a detailed understanding of the internal iliac artery branches and common variants is vital in performing revascularization and embolization procedures for conditions such as vasculogenic erectile dysfunction, high-flow priapism, and benign prostatic hyperplasia [18, 22,23,24].
The internal iliac artery arises from the common iliac artery bifurcation and descends in the pelvis to the level of the greater sciatic foramen, where it branches into the anterior and posterior trunks. The anterior division supplies the pelvic organs, while the posterior division supplies the musculature and osseous structures of the pelvis. There is significant variation in the branch pattern of these tributary arteries. A commonly used classification system created by Yamaki et al. [25] describes four distinct groups based on the branching pattern of the superior gluteal, inferior gluteal and internal pudendal arteries (Fig. 10). In the most frequent pattern of internal iliac artery branching seen in up to 80% of individuals, the common trunk of the inferior gluteal and internal pudendal arteries form the anterior division, while the superior gluteal artery forms the posterior division (Fig. 11). While it is also a major branch of the internal iliac artery, the obturator artery is not included in the Yamaki classification due to the high variability of its origin [25].
There are many branching variations of the anterior division vessels, which include the inferior gluteal, internal pudendal, superior vesical, inferior vesical, obturator and middle rectal arteries [3]. The superior vesical artery is the first branch arising from the anterior division and supplies the distal ureter, body and fundus of the bladder, proximal vas deferens and seminal vesicles. The inferior vesical artery supplies the bladder base, vas deferens and seminal vesicles and often arises from a common branch with the middle rectal artery. The internal pudendal artery is one of the terminal branches of the anterior division and gives off the perineal artery, inferior rectal artery and scrotal artery in the perineum, which supply the perineal muscle, anus and scrotum, respectively [26]. The internal pudendal artery is referred to as the penile artery within the perineum. These vessels are often too diminutive to identify on CT or MRI.
The penis is supplied by the penile artery, which consists of the bulbourethral artery, dorsal penile artery and cavernous, or deep artery. The bulbourethral artery supplies the penile bulb, glans penis, urethra and corpus spongiosum. The dorsal penile artery courses along the dorsal aspect of the corpora cavernosa and supplies the glans penis and prepuce, giving off branches to the corpus spongiosum and urethra. There are often paired cavernous arteries, one in the center of each corpus cavernosum, each giving off branches into the sinusoidal spaces. Focal lesions within the penile artery branches may result in arteriogenic erectile dysfunction [3, 27, 28].
The testis and epididymis receive arterial blood supply from three different sources. The testicular artery arises from the abdominal aorta at L2–L3 and supplies approximately two-thirds of total blood supply. The cremasteric artery arises from the inferior epigastric artery and anastomoses with the testicular artery at the lower pole of the testis. The deferential artery of the Vas can arise from the superior or inferior vesical artery. This artery supplies the vas deferens before anastomosing with the testicular artery close to the mediastinum testis [29].
The prostate artery most commonly arises from the internal pudendal artery or the common gluteal–pudendal trunk [30]. In patients with benign prostatic hyperplasia, the prostate artery branches may be enlarged, which allows for improved visibility and identification prior for patients who undergo prostate arterial embolization [31].
Pelvic musculature
The pelvic muscles function to support the abdominopelvic viscera and maintain urinary and fecal continence. The obturator internus and piriformis form a portion of the pelvic wall and function primarily as muscles of the leg (Fig. 12). The levator ani forms a large portion of the pelvic floor, dividing into the pubococcygeus, iliococcygeus, and puborectalis (Fig. 13), which each have separate attachments to the pelvic viscera; fibers from the pubococcygeus coursing inferolateral to the prostate and attaching to the perineal body are referred to as the puboprostaticus [3].
Medial fibers from the pubococcygeus course directly lateral to the urethra and the urethral sphincter while passing through the pelvic floor, assisting in urinary continence. The external urethral sphincter is striated and is able to sustain contractions for long periods. Urinary continence due to diminished sphincter dysfunction can be treated with a number of different surgical and interventional techniques [32].
The pelvic muscles are surrounded by fascia that is continuous with the perineal fascia inferiorly. The perineum is divided into an anterior urogenital triangle and posterior anal triangle by the interischial line, an arbitrary line connecting the ischial tuberosities. The urogenital triangle is divided by the perineal membrane into superficial and deep perineal spaces. In males, the superficial perineal space encompasses the scrotum and root of the penis. The ischiocavernosus muscles attach to the medial ischial tuberosity and covers the undersurface of the crus penis, converging in the dorsal penis to form the corpora cavernosa. The bulbospongiosus is found in the midline in males, consisting of two symmetric parts united by a median raphe. Bulbospongiosus fibers attach to the fibromuscular perineal body and then fan out into other structures; anterior fibers spread out over the corpora cavernosa and middle fibers surround the corpus spongiosum [33] (Fig. 14).
Conclusion
The visceral organs of the male pelvis have complex anatomic relationships with the surrounding extraperitoneal spaces, supplying arteries and adjacent pelvic musculature. Awareness of this intricate anatomy assists radiologists in the characterization of the various pathological processes that may originate in the pelvis, and improves recognition of the complex routes in which these conditions can spread.
References
Auh YH, Rubenstein WA, Schneider M, et al. Extraperitoneal paravesical spaces: CT delineation with US correlation. Radiology 1986;159:319e28.
O’connell AM, Duddy L, Lee C, Lee MJ. CT of pelvic extraperitoneal spaces: an anatomical study in cadavers. Clinical radiology. 2007 May 1;62(5):432-8.
Standring S. (2016). True pelvis, pelvic floor and perineum. Elsevier Limited (41st ed.), Gray’s Anatomy (pp 1221-1236).
Korobkin M, Silverman PM, Quint LE, Francis IR. CT of the extraperitoneal space: normal anatomy and fluid collections. AJR. American journal of roentgenology. 1992;159(5):933-42.
Salerno G, Daniels IR, Brown G. Magnetic resonance imaging of the low rectum: defining the radiological anatomy. Colorectal Disease. 2006;8:10-3.
Leffler KS, Thompson JR, Cundiff GW et al: Attachment of the rectovaginal septum to the pelvic sidewall. Am J Obstet Gynecol 2001; 185:41–43.
Mellnick VM, Balfe DM, Peterson CM (2015). Anatomy and Imaging of the Peritoneum and Retroperitoneum. Saunders (4th ed.), Textbook of Gastrointestinal Radiology (pp 1983-2005).
Auh, Y. H., Lim, J. H., & Kung, S. T. (2010). The Extraperitoneal Pelvic Compartments. In Meyers’ Dynamic Radiology of the Abdomen (pp. 203-221). Springer, New York, NY.
Kim SW, Kim HC, Yang DM, Min GE. The prevesical space: anatomical review and pathological conditions. Clinical radiology. 2013;68(7):733-40
Vaccaro JP, Brody JM. CT cystography in the evaluation of major bladder trauma. Radiographics. 2000;20(5):1373-81.
Chen N, Min PQ, Liu ZY, Wu B, Yang KQ, Lu CY. Radiologic and anatomic study of the extraperitoneal space associated with the rectum. American Journal of Roentgenology. 2010;194(3):642-52.
Mirilas P, Skandalakis JE. Surgical anatomy of the retroperitoneal spaces part II: the architecture of the retroperitoneal space. The American surgeon. 2010;76(1):33-42.
Kelley MP, Efron J, Fang SH, et al (2019). Operative Anatomy of the Colon, Rectum and Anus. In Shackelford’s Surgery of the Alimentary Tract 8th ed (pp 1662-1675). Elsevier Health Sciences.
Mastromatteo JF, Mindell HJ, Mastromatteo MF, Magnant MB, Sturtevant NV, Shuman WP. Communications of the pelvic extraperitoneal spaces and their relation to the abdominal extraperitoneal spaces: helical CT cadaver study with pelvic extraperitoneal injections. Radiology. 1997;202(2):523-30.
Peters 3rd WA, Thornton Jr WN. Surgical anatomy of the perirectal fascia: a gynecologic perspective. Obstetrical & gynecological survey. 1987;42(10):605.
Grabbe E, Lierse W, Winkler R. The perirectal fascia: morphology and use in staging of rectal carcinoma. Radiology. 1983;149(1):241-6.
Tan CH, Vikram R, Boonsirikamchai P, Faria SC, Charnsangavej C, Bhosale PR. Pathways of extrapelvic spread of pelvic disease: imaging findings. Radiographics. 2011;31(1):117-33.
Trerotola SO, Kuhlman JE, Fishman EK. CT and anatomic study of postcatheterization hematomas. Radiographics. 1991;11(2):247-58.
Loukas M, Myers C, Shah R, Tubbs RS, Wartmann C, Apaydin N, Betancor J, Jordan R. Arcuate line of the rectus sheath: clinical approach. Anatomical science international. 2008;83(3):140-4.
Pannu HK, Oliphant M. The subperitoneal space and peritoneal cavity: basic concepts. Abdominal imaging. 2015;40(7):2710-22.
Aikawa H, Tanoue S, Okino Y, Tomonari K, Miyake H. Pelvic extension of retroperitoneal fluid: analysis in vivo. AJR. American journal of roentgenology. 1998;171(3):671-7.
Mauro MA. Can hyperplastic prostate follow uterine fibroids and be managed with transcatheter arterial embolization? Radiology 2008; 246:657–658
Babaev A, Jhaveri RR. Angiography and endovascular revascularization of pudendal artery atherosclerotic disease in patients with medically refractory erectile dysfunction. J Invasive Cardiol 2012; 24:236–240
Kim KR. Embolization Treatment of High-Flow Priapism. Semin Intervent Radiol. 2016;33(3):177–181.
Yamaki K, Saga T, Doi Y, et al. A statistical study of the branching of the human internal iliac ar- tery. Kurume Med J 1998; 45:333–340
Bilhim T, Casal D, Furtado A, Pais D, O’Neill JE, Pisco JM. Branching patterns of the male internal iliac artery: imaging findings. Surgical and radiologic anatomy. 2011;33(2):151-9.
Bilhim T, Pereira JA, Fernandes L, Tinto HR, Pisco JM. Angiographic anatomy of the male pelvic arteries. American Journal of Roentgenology. 2014;203(4):W373-82.
Pereira JA, Bilhim T, Rio Tinto H, Fernandes L, Martins Pisco J. Goyri-O’Neill J. Radiologic anatomy of arteriogenic erectile dysfunction: a systematized approach. Acta Med Port 2013; 26:219–225
Mostafa T, Labib I, El-Khayat Y, El-Shahat AE, Gadallah A. Human testicular arterial supply: gross anatomy, corrosion cast, and radiologic study. Fertility and sterility. 2008;90(6):2226-30.
Bilhim T, Pisco JM, Furtado A, Casal D, Pais D, Pinheiro LC, O’Neill JE. Prostatic arterial supply: demonstration by multirow detector angio CT and catheter angiography. European radiology. 2011;21(5):1119-26.
Blue RC, Fischman AM, Rastinehad AR. Selective Arterial Prostate Embolization. Smith’s Textbook of Endourology. 2019 30:1488-94.
Chorney ET, Ramchandani P, Jaffe WI, Siegelman ES. CT and MR imaging features of artificial urinary sphincters, penile prostheses, and other devices in the male lower genitourinary tract. RadioGraphics. 2018;38(3):794-805.
Tappouni RF, Sarwani NI, Tice JG, Chamarthi S. Imaging of unusual perineal masses. American Journal of Roentgenology. 2011;196(4):W412-20.
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Luk, L., Taffel, M.T. Cross-sectional anatomy of the male pelvis. Abdom Radiol 45, 1951–1960 (2020). https://doi.org/10.1007/s00261-019-02369-6
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DOI: https://doi.org/10.1007/s00261-019-02369-6