Essential anatomy for lateral lymph node dissection
Article information
Abstract
In Western countries, the gold-standard therapeutic strategy for rectal cancer is preoperative chemoradiotherapy (CRT) following total mesorectal excision (TME), without lateral lymph node dissection (LLND). However, preoperative CRT has recently been reported to be insufficient to control lateral lymph node recurrence in cases of enlarged lateral lymph nodes before CRT, and LLND is considered necessary in such cases. We performed a literature review on aspects of pelvic anatomy associated with rectal surgery and LLND, and then combined this information with our experience and knowledge of pelvic anatomy. In this review, drawing upon research using a 3-dimensional anatomical model and actual operative views, we aimed to clarify the essential anatomy for LLND. The LLND procedure was developed in Asian countries and can now be safely performed in terms of functional preservation. Nonetheless, the longer operative time, hemorrhage, and higher complication rates with TME accompanied by LLND than with TME alone indicate that LLND is still a challenging procedure. Laparoscopic or robotic LLND has been shown to be useful and is widely performed; however, without a sufficient understanding of anatomical landmarks, misrecognition of vessels and nerves often occurs. To perform safe and accurate LLND, understanding the landmarks of LLND is essential.
INTRODUCTION
After abdominoperitoneal resection for rectal cancer was introduced in 1908 by Miles [1] to improve patients’ prognosis, extended resection accompanied by the dissection of both aortic and lateral lymph nodes (LLNs) was performed by Sauer and Bacon [2], Bacon et al. [3], and Stearns and Deddish [4] in the 1950s. However, this strategy resulted in hemorrhage and adverse effects on urinary and sexual function, and was performed less frequently. In 1982, the principle of total mesorectal excision (TME) was proposed [5], and TME was reported to reduce local recurrence [6, 7]. In addition, during the 2000s, several studies demonstrated that TME combined with preoperative chemoradiotherapy (CRT) dramatically decreased local recurrence [8–12]. Consequently, TME with CRT has become the gold-standard treatment for clinical stage II and III rectal cancers in Western countries.
In Eastern countries, the treatment of rectal cancer is different. As advanced rectal cancer below the peritoneal reflection has a higher risk of spreading to LLNs, for clinical T3 and T4 lower rectal cancer, the treatment strategy of resection combined with TME and prophylactic LLN dissection (LLND) without preoperative CRT has been developed [13–15]. This surgical approach for advanced rectal cancer has been reported to have a local recurrence rate comparable to that of TME with CRT [16]. As a result, TME with LLND without preoperative CRT has become the standard treatment for clinical stage II and III rectal cancers in Eastern countries.
However, in recent years, LLND and CRT have come to be considered not as independent treatment modalities, but as treatments that can be combined in some cases. LLND without CRT has recently been reported to reduce lateral pelvic recurrence but not central pelvic local recurrence. Therefore, in higher risk cases of rectal cancer (e.g., bulky tumors with deep penetration or threatening circumferential margins), LLND with preoperative CRT should be considered [17, 18]. On the contrary, recent studies have demonstrated that when enlarged LLNs were present in pre-CRT situations, CRT was insufficient to control LLN recurrence; in those cases, LLND with CRT has been considered to achieve local control [19–24]. From this standpoint, the combination of CRT and LLND has become an important future therapeutic strategy for advanced rectal cancer, and training in LLND has become necessary for colorectal surgeons in both Western and Eastern countries.
As aforementioned, extended resection including LLNs resulted in increased postoperative dysfunction [2–4]. In an attempt to improve this, an autonomic nerve preservation technique was developed in Japan [25]. Consequently, LLND can be safely performed in terms of function preservation. A randomized controlled trial in Japan comparing LLND and non-LLND for clinical stage II or III rectal cancer showed comparable rates of postoperative sexual and urinary dysfunction [17]. However, LLND remains challenging because of a longer operative time, higher risk of hemorrhage, and a marginally higher rate of grade III or IV complications with LLND than without LLND [17]. Laparoscopic and robotic surgery has recently become popular worldwide, and LLND has gradually evolved from an open technique to a laparoscopic or robotic approach. The safety and feasibility of these minimally invasive approaches for LLND have been demonstrated [26, 27]. The laparoscopic magnified view enables surgeons to identify small vessels, nerves, and fascial laminations invisible to the naked eye in conventional open surgery; however, without a sufficient understanding of anatomical landmarks, misrecognition of vessels and nerves often occurs. Therefore, in this review, we aimed to clarify the essential anatomy for LLND drawing upon research using a 3-dimensional anatomical model and actual operative views from our institution, The University of Tokyo (Tokyo, Japan).
Ethics statement
The study was approved by the Institutional Review Board of The University of Tokyo (No. 3252-15). Written informed consents for publication of the research details were obtained.
DEFINITION OF LLN
In Japan, the Japanese Classification of Colorectal Carcinoma categorizes LLNs as internal iliac lymph nodes (#263), obturator lymph nodes (#283), external iliac lymph nodes (#293), common iliac lymph nodes (#273), aortic bifurcation lymph nodes (#280), and midline sacrum lymph nodes (#270) (Fig. 1) [28]. The metastasis rate in LLN-positive cases has been previously reported [29]. Among LLNs, the internal iliac lymph nodes showed the highest rate of metastasis. The metastasis rate differs on either side of the superior vesical artery, which is a branch of the internal iliac artery; the frequencies were 26% on the proximal side of the superior vesical artery and 47% on the distal side. The obturator lymph nodes are the second most common region of metastasis, which occurs in 38% of cases. The frequency of metastasis in other areas (e.g., the external iliac lymph nodes, common iliac lymph nodes, and aortic bifurcation/midline sacrum lymph nodes, was much lower, with a total frequency of 7.7%). Based on these data, the target lymph nodes for prophylactic LLND were defined in the Japanese Classification of Colorectal Carcinoma as internal iliac and obturator lymph nodes. Therefore, in this review, we describe the essential anatomy for resecting these 2 regions of lymph nodes.
ESSENTIAL LANDMARKS FOR LLND
Accurate and safe LLND requires an understanding of the lateral, internal, dorsal, and caudal planes of the LLN region. The anatomical structures that comprise these respective planes are as follows: lateral plane (external iliac artery and vein and internal obturator muscle), internal plane (pelvic plexus and bladder), dorsal plane (internal iliac artery and vein, piriform muscle, and sacral plexus), and caudal plane (coccygeal muscle and levator ani muscle).
Fig. 2A shows the anatomy of the lateral, dorsal, and caudal planes of the LLN region [30]. After giving rise to parietal branches, such as the superior and inferior gluteal arteries, and visceral branches, such as the umbilical and superior/inferior vesical arteries, the internal iliac artery flows into the Alcock canal as the internal pudendal artery. The branch patterns of the internal iliac artery are variegated [31]. The following is the most common type: the internal iliac artery first gives rise to the superior gluteal arteries and visceral arteries, before branching into the inferior gluteal artery and internal pudendal artery, which then exit the pelvis through the greater sciatic foramen and Alcock canal, respectively (Fig. 2A) [30]. In some cases, this branching to the inferior gluteal artery and internal pudendal artery occurs after the internal iliac artery flows out between the piriform and coccygeus muscles. When this happens, the gluteal-pudendal trunk comprises the dorsal plane of LLND. The Alcock canal is enclosed between the piriform and coccygeus muscles. Through the Alcock canal, the pudendal nerve, which is a branch of the sacral plexus, traces through the pelvis along with the internal pudendal artery. In the aforementioned figure, to clearly understand the lateral, dorsal, and caudal planes of the LLN region, the branches of the internal iliac artery, pelvic plexus, and ureter were eliminated. The levator ani, which comprises the caudal edge, and the internal obturator muscle, which comprises the lateral edge, are bounded by the tendinous arch of the levator ani. Fig. 2B [30] shows the lateral, dorsal, and caudal planes of the LLND.
The medial plane of the obturator lymph node region is the vesicohypogastric fascia, which means that the internal iliac and obturator lymph node regions are bounded by the vesicohypogastric fascia (Fig. 3A) [30]. Understanding the vesicohypogastric fascia is essential when performing LLND [32–34]. The vesicohypogastric fascia is a triangular fascia that stands out from the internal iliac artery along the umbilical artery and the lateral border of the bladder. It is a double-layer sheet surrounding the branches of the internal iliac artery, such as the umbilical, superior/inferior vesical, and uterine arteries (Fig. 3A) [30]. The vesicohypogastric fascia is united with the Gerota capsule in the cranial direction. The obturator artery, vein, and nerve are shown in Fig. 3B [30]. The fat tissue surrounded by the lateral plane (composed of the external iliac artery and vein and internal obturator muscle), the dorsal plane (composed of the internal iliac artery and vein, piriform muscle, and sacral plexus), and the medial plane (the vesicohypogastric fascia) should be dissected for the obturator lymph node. The obturator artery, vein, and nerve run through this region (Fig. 3B) [30].
The internal plane of LLND, which is identical to the internal plane of the internal iliac lymph node region, comprises the ureterohypogastric fascia, which is also known as the prehypogastric nerve fascia [33, 34]. As its name suggests, tracing the fascia proximally and ventrally leads to the ureter. The ureterohypogastric fascia is the border between the mesorectum and LLN region. This fascia includes the hypogastric nerve and pelvic plexus and joins the Denonvilliers’ fascia at the anterolateral aspect (Fig. 4) [30]. At the anterolateral aspect, branches of the pelvic plexus, which run through the ureterohypogastric fascia, compose a bundle with genital blood vessels that run through the vesicohypogastric fascia. This bundle is called the neurovascular bundle (NVB). Similar to the vesicohypogastric fascia, the ureterohypogastric fascia is united with the Gerota capsule in the cranial direction. Both the fat tissue included in the vesicohypogastric fascia itself and that between the vesicohypogastric fascia and ureterohypogastric fascia include the internal iliac lymph nodes.
Considering the caudal plane of LLND, the tendinous arch of the pelvic fascia is also important. Little has been reported regarding the relationship between the vesicohypogastric fascia, ureterohyogastric fascia, and the tendinous arch of the pelvic fascia. Occelli et al. [35] described the tendinous arch of the pelvic fascia as a thickening of the fascia of the levator ani muscle, which extends from the internal end of the pubic insertion of the levator ani to the internal aspect of the ischiatic spine. They also mentioned that the posterior third of the tendinous arch of the pelvic fascia is fused with the posterior third of the tendinous arch of the levator ani. Pit et al. [36] explained that the tendinous arch of the pelvic fascia results from thickening of the endopelvic fascia, which is firmly attached to the posterolateral part of the ureter via fibrous tissues. This means that the ureterohypogastric fascia is fused with the tendinous arch of the pelvic fascia. The ureterohypogastic fascia, vesicohypogastric fascia, and mesorectal fascia unite below the S4 level [37]. From these anatomical studies, the tendinous arch of the pelvis is considered to be the fusion point of the ureterohypogatric fascia, vesicohypogastric fascia, mesorectal fascia, and the fascia of the levator ani (Fig. 2A) [30]. During LLND, surgeons dissect the fusion point to connect the dissection region of the lateral lymph node region to the dissection region of TME. Fig. 5 [30] shows the relationship between the vesicohypogastric fascia, ureterohypogastric fascia, obturator lymph node region, and internal iliac lymph node region.
NEUROVASCULAR BUNDLE
Understanding the anatomy of the NVB is essential both for LLND and rectal cancer surgery. Comprehension of the vesicohypogastric and ureterohypogastric fasciae leads to an understanding of the anatomy of the NVB. The hypogastric and pelvic nerves connect with each other in the ureterohypogastric fascia and form the pelvic plexus. The ureterohypogastric fascia fuses with Denonvilliers’ fascia on the anterolateral side of the rectum. Rectal branches from the pelvic plexus and occasionally the middle rectal artery run through this area to the rectum, forming the lateral ligament of the rectum [38–41]. However, in anatomical studies, the ligamentous component was not recognized, so the lateral ligament was considered to be a dense adhesion between the fascia, rectal branches of the pelvic plexus, and middle rectal artery [38–41]. After branching from the rectal branches, the pelvic plexus runs in 3 directions: ventrally (passing near the seminal vesicle and distributed throughout the bladder); runs ventrally and caudally (passing between the prostate and seminal vesicle, and distributed along the side wall of the prostate); and caudally (passing near the rectum and through the posterolateral side of the prostate, and distributed to the corpus cavernosum of the penis) (Fig. 6A) [30, 42]. This last branch of the pelvic plexus, jointly with small vessels of the genital branches of the internal iliac artery (distal branches of the superior and inferior vesicle artery), which run through the vesicohypogastric fascia, comprises the NVB (Fig. 6B) [30]. This means that the vesicohypogastric and ureterohypogastric fasciae fuse with each other and comprise the NVB at the anterolateral aspect of the rectum (Fig. 6C) [30]. These fused fasciae unite with the Denonvilliers’ fascia on the dorsal side of the prostate.
Understanding the essential anatomy of LLND is important for understanding the anatomy of rectal surgery. Fig. 7 shows the 3-dimensional printed pelvic anatomy of all structures except the pelvic plexus and hypogastric nerve [30, 43]. This anatomy should be understood to ensure safe and accurate LLND.
PROCEDURE FOR LLND
Using actual images from robotic surgery, the following section presents an explanation of the dissection procedure at our hospital and the landmarks of dissection. As aforementioned, complete LLND requires complete resection of the obturator (#283) and internal iliac (#263) lymph nodes. The choice of the first lymph node region to be dissected differs among institutions. At our institution, the obturator lymph node is dissected first.
Expose the lateral edge of the obturator lymph node region
LLND is performed after the completion of TME for the primary lesion. First, the ureter is taped, and the ureterohypogastric fascia is separated from the internal fatty tissue, which includes the internal lymph nodes, by retracting the taped ureter medially. The incision is extended caudally and medially until it joins the dissection part of TME. This maneuver is important for preserving the autonomic nerve and obtaining a sufficient surgical view for dissection of the obturator lymph nodes.
The dissection is then started lateral to the obturator nodes. The external iliac artery and vein are exposed. The external iliac vein is located on the dorsal side of the artery. After retracting the external iliac vein laterally with a blunt instrument, the fatty tissues are peeled from the psoas and internal obturator muscles. By continuing the dissection caudally, the internal obturator muscle, obturator foramen, and obturator artery, vein, and nerve that flow into the obturator foramen can be identified. The obturator artery and vein are then divided. When an accessory obturator vein flows into the external iliac vein, it is also divided (Fig. 8A) [30]. The dissection continues in a caudal direction until it reaches the tendinous arch of the levator ani and that of the pelvis fascia. Here, it denotes the caudal edge of the obturator lymph node region (Fig. 8B) [30].
Expose the dorsal and internal edges of the obturator lymph node region
The internal edge of the obturator lymph node region is the vesicohypogastric fascia. When identifying the umbilical artery and superior and inferior vesical artery, these arteries form a fascia-like structure. This is the vesicohypogastric fascia. Next, the umbilical or vesical artery is retracted medially and caudally, the fat tissue is separated from the vesicohypogastric fascia in line with the side wall of the bladder, and then the tendinous arch of the levator ani and that of the pelvic fascia, which form the caudal edge of the obturator lymph node, are reached (Fig. 8C) [30].
The dorsal edge of the obturator lymph node region is composed of the internal iliac artery and vein, piriform muscle, and sacral plexus. The fatty tissue is peeled away in line with the internal iliac artery, and then the obturator artery and vein, which branches from the internal iliac artery, is identified. The obturator artery and vein are divided for a second time at their origin. The obturator nerve is preserved, and dissection is continued along the sacral plexus and internal iliac artery to reach the Alcock canal. The obturator lymph nodes are completely removed from the obturator compartment. Fig. 8D [30] shows the completion of obturator lymph node dissection.
Expose the internal edge of the internal lymph node region
Internal lymph nodes exist between the vesicohypogastric fascia and ureterohypogastric fascia. To prevent injury to the hypogastric nerve, the ureterohypogastric fascia, including the ureter and hypogastric nerves, is first separated when LLND is performed (Fig. 9A) [30]. The ureter is retracted medially, the vesicohypogastric fascia is retracted laterally, and fatty tissues are peeled from the internal iliac artery branches (e.g., the umbilical artery and superior/inferior vesical artery) until the Alcock canal is observed. When lymph node metastasis is suspected between the vesicohypogastric fascia, the superior and inferior vesical arteries are divided with the lymph nodes. However, dissection of the vesical artery has been reported to increase the rate of postoperative urinary dysfunction [44]; therefore, if there is no apparent lymph node metastasis in the vesicohypogastric fascia, the vesical arteries are preserved. As aforementioned, among the LLNs, the internal iliac lymph nodes on the distal side of the superior vesical artery have a high metastasis rate; hence, complete resection of the fatty tissue in this region is important [28]. Fig. 9B [30] shows a view of completed dissection of the internal iliac lymph nodes.
CONCLUSION
We conducted a review of the essential anatomy of LLND. As the procedure poses challenges, it is crucial to achieving radical resection and preservation of genital function. Particularly in laparoscopic and robotic surgery, misunderstanding the anatomy for LLND easily leads to misrecognizing vessels and nerves. Therefore, to perform safe and accurate LLND, a thorough understanding of the landmarks for the LLND procedure is essential.
Notes
Conflict of interest
No potential conflict of interest relevant to this article was reported.
Funding
This work was supported by Grant-in-Aid for Scientific Research (C) (No. 18K07194, 19K09114, 19K09115, 20K09051), Grant-in-Aid for Challenging Research (Exploratory) (No. 20K21626), and Grant-in-Aid for Scientific Research (B) (No. 21H02778) from the Japan Society for the Promotion of Science. This work was also supported by the Project for Cancer Research and Therapeutic Evolution (P-CREATE) (No. JP 19cm0106502) from the Japan Agency for Medical Research and Development (AMED).
Author contributions
Conceptualization: YY, SI; Data curation: YY, HN, KS, KM, SE; Investigation: YY, HM, SA, YN, YY, TS, HS; Methodology: YY, DH; Project administration: SI; Writing-original draft: YY; Writing-review & editing: all authors. All authors read and approved the final manuscript.