全直肠系膜切除相关盆自主神经的解剖学观察

目的：阐述全直肠系膜切除术相关盆自主神经的局部解剖学特点，探讨盆自主神经保留的部位和对策。方法：对20具男性盆腔固定标本进行解剖观察。结果：腹主动脉丛远离肠系膜下动脉起点；上腹下丛贴近骶岬表面；腹下神经部分毗邻输尿管；盆内脏神经伴行直肠中动脉外侧部；下腹下丛位于直肠系膜后外侧；其直肠侧支走行于直肠侧韧带内，直肠前支向前穿过Denonvilliers筋膜后叶；勃起神经位于Denonvilliers筋膜前叶外侧部。结论：盆自主神经保留的部位是：离断肠系膜下血管时的腹主动脉丛左干，直肠后分离时的上腹下丛和腹下神经，直肠侧面分离时的下腹下丛和盆内脏神经，直肠前分离时的勃起神经。共同原则是：在直肠后间隙中贴近直肠系膜操作；直视下操作；避免过度牵引直肠系膜。     

Topography of the pelvic autonomic nervous system and its potential impact on surgical intervention in the pelvis

Bladder, bowel, and sexual dysfunction caused by iatrogenic lesions of the inferior hypogastric plexus (IHP) are well known and commonly tolerated in pelvic surgery. Because the pelvic autonomic nerves are difficult to define and dissect in surgery, and their importance often ignored, we conducted a gross anatomic study of 90 adult and four fetal hemipelves. Using various non-surgical approaches, the anatomic relations and pathways of the IHP were dissected. The IHP extended from the sacrum to the genital organs at the level of the lower sacral vertebrae. It originated from three different sources: the hypogastric nerve, the sacral splanchnic nerves from the sacral sympathetic trunk (mostly the S2 ganglion), and the pelvic splanchnic nerves, which branched primarily from the third and fourth sacral ventral rami. These fibers converge to form a uniform nerve plate medial to the vascular layer and deep to the peritoneum. The posterior portion of the IHP supplied the rectum and the anterior portion of the urogenital organs; nerve fibers traveled directly from the IHP to the anterolateral wall of the rectum and to the inferolateral and posterolateral aspects of the urogenital organs. The autonomic supply from the IHP was supplemented by nerves accompanying the ureter and the arteries. An understanding of the location of the autonomic pelvic network, including important landmarks, should help prevent iatrogenic injury through the adoption of surgical techniques that reduce or prevent postoperative autonomic dysfunction.     

An anatomical investigation on the muscles of the pelvic outlet in crab-eating monkey (Macaca irus) and Japanese monkey (Macaca fuscata) with special reference to their nerve supply

For a fuller understanding of the nerve supply to the muscles of the pelvic outlet in man, 4 pelvic-halves of crab-eating monkeys and 6 pelvic-halves of Japanese monkeys were minutely dissected. 1) The composition of the pudendal plexus tends to be limited to 2 segments, S1 and S2. 2) If we consider the origin of the nerves, the pudendal plexus is divided into 2, the first or medial and the second or lateral parts. From the first part arise the pelvic splanchnic nerves, the nerve to the iliopubocaudalis and the nerve to the ischiocaudalis. From the second part the dorsal nerve of the penis or clitoris, the perineal nerve and the inferior rectal nerve originate. 3) A laminate arrangement exists among the 3 nerves from the first part at their origin; the pelvic splanchnic nerves are situated ventrally, and the nerve to the ischiocaudalis dorsally, with the nerve to the iliopubocaudalis in between. No obvious laminate arrangement exists among the 3 nerves from the second part. 4) The part of the iliopubocaudalis, contiguous with the rectal wall but without attaching to it, has no branches of supply from the perineal nerve and the inferior rectal nerve. 5) A detailed discussion of our findings in relation to man, is given below.     

The vascular and neuronal composition of the lateral ligament of the rectum and the rectosacral fascia

Summary Detailed dissections were performed on 83 pelvic halves from 45 cadavers in order to obtain more accurate data on the composition of the lateral ligament of the rectum and the rectosacral fascia. The middle rectal artery was observed in only 18 out of 81 spcimens (22.2%). The lateral ligament of the rectum was divided into lateral and medial portions, according to the positional relationship to the pelvic plexus. The lateral part consisted of a superoanterior and an inferoposterior subdivision. The main component of the former was the middle rectal artery, while the pelvic splanchnic nerves were contained in the latter. Both components can be considered to contribute to the formation of the medial part, although the middle rectal vessels were not always present. The medial part consisted of the rectal branches from the pelvic plexus and their connective tissue. The rectosacral fascia was formed by dense connective tissue between the posterior wall of the rectum and the third and fourth sacral vertebrae. The main components of the fascia were branches of the lateral and median sacral vessels and the sacral splanchnic nerves which arose directly from the sacral sympathetic ganglia.

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La structure du ligament latéral du rectum et du fascia recto sacré

Résumé La dissection de 83 hémibassins provenant de 45 cadavres a été réalisée pour préciser la structure du ligament latéral du rectum et du fascia recto sacré. L'artère rectale moyenne (ARM) a été observée seulement sur 18 specimens (22,2 %). Le ligament latéral du rectum a été divisé en portion latérale et médiale, en fonction des rapports topographiques avec le plexus pelvien. La partie latérale présente une portion antérosupérieure contenant l'ARM et une portion postéro-inférieure contenant les nerfs splanchniques pelviens (NSP). Ces deux composants (ARM et NSP) contribuent à la formation de la partie médiale bien que les vaisseaux rectaux moyens ne soient pas toujours présents. La partie médiale répond aux branches rectales du plexus pelvien et à leurs tissus conjonctifs environnants. Le fascia sacro-rectal est formé de tissu conjonctif dense, tendu de la paroi postérieure du rectum aux 3e et 4e vertèbres sacrées. Les principaux composants de ce fascia sont les branches latérales et médiales des vaisseaux sacrés et les nerfs splanchniques sacrés arrivant directement des ganglions sympathiques sacrés.

     

Extrinsic innervation of the pelvic organs in the lesser pelvis of human embryos

Realistic models to understand the developmental appearance of the pelvic nervous system in mammals are scarce. We visualized the development of the inferior hypogastric plexus and its preganglionic connections in human embryos at 4–8 weeks post-fertilization, using Amira 3D reconstruction and Cinema 4D-remodelling software. We defined the embryonic lesser pelvis as the pelvic area caudal to both umbilical arteries and containing the hindgut. Neural crest cells (NCCs) appeared dorsolateral to the median sacral artery near vertebra S1 at ~5 weeks and had extended to vertebra S5 1 day later. Once para-arterial, NCCs either formed sympathetic ganglia or continued to migrate ventrally to the pre-arterial region, where they formed large bilateral inferior hypogastric ganglionic cell clusters (IHGCs). Unlike more cranial pre-aortic plexuses, both IHGCs did not merge because the 'pelvic pouch', a temporary caudal extension of the peritoneal cavity, interposed. Although NCCs in the sacral area started to migrate later, they reached their pre-arterial position simultaneously with the NCCs in the thoracolumbar regions. Accordingly, the superior hypogastric nerve, a caudal extension of the lumbar splanchnic nerves along the superior rectal artery, contacted the IHGCs only 1 day later than the lumbar splanchnic nerves contacted the inferior mesenteric ganglion. The superior hypogastric nerve subsequently splits to become the superior hypogastric plexus. The IHGCs had two additional sources of preganglionic innervation, of which the pelvic splanchnic nerves arrived at ~6.5 weeks and the sacral splanchnic nerves only at ~8 weeks. After all preganglionic connections had formed, separate parts of the inferior hypogastric plexus formed at the bladder neck and distal hindgut.     

Systematization of the vesical and uterovaginal efferences of the female inferior hypogastric plexus (pelvic): applications to pelvic surgery on women patients

Objective To locate and describe the various efferences of the plexus in order to make it easier to avoid nerve lesions during pelvic surgery on women patients through a better anatomical knowledge of the inferior hypogastric plexus (IHP). Materials and methods We dissected 27 formalin embalmed female anatomical subjects, none of which bore any stigmata of subumbilical surgery. The dissection was always performed using the same technique: identification of the inferior hypogastric plexus, whose posterior superior angle follows on from the hypogastric nerve and whose top, which is anterior and inferior, is located exactly at the ureter’s point of entry into the base of the parametrium, underneath the posterior layer of the broad ligament. Results The IHP is located at the level of the posterior floor of the pelvis, opposite to the sacral concavity. Its top, which is anterior inferior, is at the point of contact with the ureter at its entry into the posterior layer of the broad ligament. The uterovaginal, vesical and rectal efferences originate in the paracervix. Three efferent nerves branch, two of them from its top and the third from its inferior edge: (1) A vaginal nerve, medial to the ureter, follows the uterine artery and divides into two groups: anterior thin, heading for the vagina and the uterus; posterior, voluminous, heading in a superior rectal direction (=superior rectal nerve). (2) A vesical nerve, lateral to the ureter, divides into two groups, lateral and medial. (3) The inferior rectal nerve emerges from the inferior edge of the IHP, between the fourth sacral root and the ureter’s point of entry into the base of the parametrium. Conclusion The ureter is the crucial point of reference for the IHP and its efferences and acts as a real guide for identifying the anterior inferior angle or top of the IHP, the origin of the vaginal nerve, the level of the ureterovesical junction and the division of the vesical nerve into its two medial and lateral branches. Dissecting underneath and inside the ureter and the uterine artery involves a risk of lesion of the vaginal nerve and its uterovaginal branches. Further forward, between the intersection and the ureterovesical junction, dissecting and/or coagulating under the ureter involves a risk of lesions to the vesical nerve, which are likely to explain the phenomena of denervation of the anterior floor encountered after certain hysterectomies and/or surgical treatments of vesicoureteral reflux.     

Topological changes of the human autonomic cardiac nervous system in individuals with a retroesophageal right subclavian artery: two case reports and a brief review

The topological changes of the human autonomic cardiac nervous system in two cadavers with a retroesophageal right subclavian artery (Rersa) were compared with the normal autonomic cardiac nervous system. The following new results were obtained in addition to the conventional deficient finding of the right recurrent laryngeal nerve. (1) Right superior cardiac nerves arising from the superior cervical ganglion were consistently observed in both cadavers, in addition to the right thoracic cardiac nerves along the Rersa. (2) A segmental accompanying tendency of the right cardiac nerves was recognized: the cardiac nerves arising from the sympathetic trunk cranial to the middle cervical ganglia ran along with the right common carotid artery, whereas the cardiac nerves arising from the sympathetic trunk caudal to the vertebral ganglion ran along the Rersa. (3) The right thoracic cardiac nerves, which have never been observed to accompany the normal right subclavian artery, ran along the proximal part of the Rersa. According to previous reports of individuals with the Rersa, a thick right thoracic cardiac nerve is commonly observed instead of a right superior cardiac nerve. However, all the cardiac nerves were recognized in both the individuals described in the present report. Therefore, we strongly disagree with the previous idea that the origin of the right cardiac nerves from the sympathetic trunk and ganglia is shifted caudally in individuals with the Rersa. The topological changes of the autonomic cardiac nervous system in two cases of Rersa also reflected spatial changes of great arteries.     

腹腔镜入路骶神经电刺激器植入的解剖学特点及其临床意义

目的　讨论腹腔镜下骶前方植入骶神经电刺激电极手术入路解剖及手术可行性。 方法　在20具成人尸体标本上模拟腹腔镜下显露骶骨前第2~4骶神经前支手术,观察骶骨前方第2~4骶神经前支的形态特征和骶孔周围可能损伤重要血管的区域。 结果　第2~4骶神经前支出骶前孔至汇成骶丛的长度：S2左(32.62±3.15) mm,右(31.46±3.28) mm;S3左(21.96±2.59) mm,右(20.61±3.14) mm;S4左(15.04±1.64) mm,右(16.09±1.38) mm。骶外侧动脉的脊支动脉进入骶前孔的方位主要为内上象限。臀下动脉穿过神经时比较偏外侧靠近神经汇合处。骶椎旁静脉在第2~4骶前孔处与骶外侧动脉伴行,脊支静脉出骶前孔的位置与动脉一致。 结论　骶骨前方第2~4骶神经前支游离的长度能够达到硬膜外型骶神经电刺激器电极植入的要求。手术中骶前孔内侧为血管易损伤的危险区域。     

扩大根治性直肠切除术的应用解剖

目的:为临床扩大根治性直肠切除术提供解剖学资料。方法:对８具成人尸体标本的直肠侧方淋巴结等进行解剖观察。结果:８具标本盆腔解剖结构辩认清楚,明确了直肠侧方各组淋巴结的解剖定位。侧方向淋巴结包括前、后、中、下组,分别沿相关的血管分布。在直肠周围脂肪与盆壁之间存在着直肠后间隙,脏层筋膜所包绕的直肠周围脂肪、血管及淋巴管即为直肠系膜。腹下神经沿输尿管和髂内动脉向侧、尾方走行,并于发自Ｓ２~４神经根的盆内脏神经在盆腔侧壁汇合成盆自主神经。结论:低位直肠癌的转移特点是直肠上方向和侧方向淋巴结转移,扩大根治性直肠切除术有助于降低低位直肠癌术后的局部复发,提高远期疗效。     

直肠癌手术相关腹膜后自主神经的筋膜解剖学观察

目的　从临床解剖学和组织学角度进一步阐明盆自主神经的筋膜层次。 方法　选取7具尸体标本和52例接受腹腔镜直肠癌切除手术的病人,观察其自主神经与肾前筋膜-骶前筋膜的关系。切取尸体降乙结肠系膜与主髂动脉之间、直肠系膜与骶骨骨膜之间的腹膜后组织做组织学检查。 结果　解剖学观察显示,腹主动脉丛、上腹下丛、腹下神经、下腹下丛位于肾前筋膜-骶前筋膜后外侧。组织学检查显示：神经纤维位于筋膜后,部分较细的纤维位于筋膜内。 结论　自主神经位于肾前筋膜-骶前筋膜后外侧。保持这一筋膜的完整性,是直肠癌手术中保护自主神经的解剖学基础和基本方法。     

The relationship of the posterior inferior cerebellar artery to cranial nerves VII-XII

The posterior inferior cerebellar artery (PICA) is the largest branch of the vertebral artery. It usually arises at the anterolateral margin of the medulla oblongata close to the lower cranial nerves. The PICA had the most complex relationship to the cranial nerves of any artery and it is frequently exposed in approaches directed to the fourth ventricle. The aim of this article is to describe the anatomical relationship of the PICA to the lower cranial nerves. In this study, 12.5% of PICAs passed between the glossopharyngeal and vagus nerves, 20% between the vagus and accessory nerves, and 65% through the rootlets of the accessory nerve. The lateral medullary segment of the PICA showed a lateral loop which in 20% specimens pressed against the inferior surfaces of the facial and vestibulocochlear nerves. The lateral medullary segment of the PICA in 20% specimens passed superior to the hypoglossal nerve, in 47.5% through the rootlets of the hypoglossal nerve, and in 30% inferior to the hypoglossal nerve. The findings on the relationship of the PICA to the lower cranial nerves could be helpful in microsurgery of this region.     

肠系膜下动脉根部自主神经保护的解剖学基础

目的　观察肠系膜下动脉（IMA）根部与其周围自主神经的解剖学关系,为肠系膜下动脉根部自主神经保护提供解剖学证据。 方法　7例10%福尔马林固定标本进行大体解剖及显微解剖;2例新鲜标本模拟腹腔镜下直肠癌D3根治术中肠系膜下动脉根部自主神经的显露和保护。 结果　上腹下丛(SHP)的左、右侧束及束间交通支与肠系膜下动脉根部关系密切。右侧束距离肠系膜下动脉根部较远,位于肾前筋膜下。以左侧束降支为界,其近端,上腹下丛左侧束、肠系膜下丛、腹主动脉丛紧贴肠系膜下动脉根部左侧壁并相互延续,其远端左侧束走行于肾前筋膜下。左侧束降支距离IMA起点的距离不恒定。 结论　在肾前筋膜前平面分离可有效保护上腹下丛右侧束及侧束间交通支;以SHP左侧束降支作为肠系膜下动脉根部离断的解剖学标志可以有效保护左侧束。     

A review of the thoracic splanchnic nerves and celiac ganglia

Anatomical variation of the thoracic splanchnic nerves is as diverse as any structure in the body. Thoracic splanchnic nerves are derived from medial branches of the lower seven thoracic sympathetic ganglia, with the greater splanchnic nerve comprising the more cranial contributions, the lesser the middle branches, and the least splanchnic nerve usually T11 and/or T12. Much of the early anatomical research of the thoracic splanchnic nerves revolved around elucidating the nerve root level contributing to each of these nerves. The celiac plexus is a major interchange for autonomic fibers, receiving many of the thoracic splanchnic nerve fibers as they course toward the organs of the abdomen. The location of the celiac ganglia are usually described in relation to surrounding structures, and also show variation in size and general morphology. Clinically, the thoracic splanchnic nerves and celiac ganglia play a major role in pain management for upper abdominal disorders, particularly chronic pancreatitis and pancreatic cancer. Splanchnicectomy has been a treatment option since Mallet‐Guy became a major proponent of the procedure in the 1940s. Splanchnic nerve dissection and thermocoagulation are two common derivatives of splanchnicectomy that are commonly used today. Celiac plexus block is also a treatment option to compliment splanchnicectomy in pain management. Endoscopic ultrasonography (EUS)‐guided celiac injection and percutaneous methods of celiac plexus block have been heavily studied and are two important methods used today. For both splanchnicectomies and celiac plexus block, the innovation of ultrasonographic imaging technology has improved efficacy and accuracy of these procedures and continues to make pain management for these diseases more successful. Clin. Anat. 23:512–522, 2010. © 2010 Wiley‐Liss, Inc.     

Exposure of the Middle Rectal Artery and Lateral Ligament of the Rectum Following the Gate Approach during Total Mesorectal Excision

Controversial surgical anatomical landmarks in the deep pelvis can be visualized and identified using current technologies. Performing the gate approach technique during deep lateral dissection for total mesorectal excision facilitates visualization of the pelvic neurovascular structures following simple dissection steps to preserve the pelvic autonomic nerves and avoid accidental vascular injuries. Here, we discuss laparoscopic exposure of an infrequent disposition of the middle rectal artery anterior to the lateral ligament of the rectum while performing the gate approach.     

Nerve contributions to the pelvic plexus and the umbilical cord

Serial sections of human embryos and fetuses reveal that the sacral nerves which contribute fibers to the pelvic plexus often have dorsal, ventral, and oblique communicating rami. The ventral rami resemble the white rami of upper thoracic nerves and some of their fibers pass close by or through the chain ganglia and into the pelvic plexus. The sizes of the ventral rami are often in inverse proportion to that of the pelvic splanchnic nerves. That is, when the pelvic splanchnic nerves are poorly developed, the ventral rami are large, and conversely, when the pelvic splanchnic nevers are well developed, these rami are small. The pelvic plexus was found to receive fibers from the sympathetic trunk and its ganglia in addition to those from the hypogastric plexus and the pelvic splanchnic nerves. Analysis of the observations made in this study together with a review of the literature in light of the present day classification of nerve fibers raises serious doubts concerning the limits set for the outflow of preganglionic nerve fibers from the spinal cord and the distribution of gray and white rami as described in recent textbooks in terms of their histological and physiological significance. Nerve fibers from the pelvic plexus can be traced along the walls of the bladder and the urachus and along the umbilical arteries into the umbilical cord. In embryos, only a few scattered nerve fibers were found distal to the umbilicus, but in fetuses at term, distinct nerve bundles were identified in the cord. These bundles sent branches to the walls of the umbilical arteries; other branches terminated as “end-nets” in Wharton's jelly. These nets appeared as fine fibers with nodular swellings at irregular intervals. Innervation of the umbilical arteries was richest within the first few inches of the cord. Beyond this region, the nerves rapidly decreased in number. “End-nets” were present as far as four inches from the umbilicus. Granular cells resembling Langerhans' cells were found in the cord. Often these cells were closely associated with fine nerve fibers.     

The posterior sacral foramina: an anatomical study

The vascular and nervous structures and their relations with the spinal nerve roots were examined in the 2nd, 3rd and 4th posterior sacral foramina in relation to percutaneous needle insertion for neuromodulation. A foraminal branch provided by the lateral sacral artery to each foramen entered the inferior lateral quadrant of each foramen, adjacent to the nerve root medially. Facing the posterior sacral aperture and around the sacral nerves, there was no venous plexus. A venous plexus was sometimes present near the median line, and always around the proximal part of the spinal ganglion. The sacral nerve roots, especially the 3rd, had a long extradural course in the foramen, presenting a potential risk of nerve lesions during procedures involving needle insertion.     

Anatomy and blood supply of the coeliac-superior mesenteric ganglion complex of the rat

Summary The anatomy of the coeliac-superior mesenteric ganglion (CSMG) complex of 28 female Wistar rats was studied by serial paraffin sections and found to be consistent in composition and in relations. The CSMG comprises two suprarenal ganglia in continuity with the major splanchnic nerves, these continuing as splanchnic trunks into paired coeliac ganglia. The left coeliac ganglion is larger than the right as it has a superior mesenteric component related to the artery of that name. Lastly, intermesenteric ganglia are related to the renal and ovarian arteries and to the origin of the intermesenteric nerves.Ink injections and microvascular casts indicate that the main extrinsic blood supply to the CSMG is derived from the inferior phrenic artery, a branch of which enters the complex at the suprarenal ganglia and supplies the CSMG via the splanchnic trunks. Also, recurrent branches of the ovarian arteries enter the intermesenteric nerves to supply the complex at its caudal pole. A few small arteries not associated with nerves and probably derived from lumbar arteries also supply the CSMG complex. The two major postganglionic nerve trunks have an abundant vasculature in continuity with that of the CSMG but whose origin and direction of blood flow has yet to be determined.     

An anomalous case of the thoracic cardiac nerve in the Japanese monkey

A rare case of an anomalous right thoracic cardiac nerve that directly distributed to the left ventricle and left coronary artery was observed in a Japanese monkey. Its nerve arose from 4th and 5th thoracic ganglia on the right sympathetic trunk, descended obliquely along the thoracic vertebra toward the thoracic aorta at the level of the body of 7th thoracic vertebra. After reaching the aorta, it reflected upward and ascended along the medial-ventral surface of the aorta. Thereafter, it received a cardiac branch arising from the vagus nerve in the upper part of the thoracic aorta, and ran to the left-lateral aspect of the heart. Finally, it gave off main branches to the terminal part of the left coronary artery and the left ventricle, and small branches to the proximal part of the left coronary artery. In a human dissection, similar nerves (the thoracic splanchnic nerve or thoracic pulmonary nerve) originating at the thoracic ganglia and reaching to the lung, have also been observed. The superior, middle and inferior cervical cardiac nerves can easily reach the heart along the common carotid artery, the brachiocephalic artery and subclavian artery. But it is not easy for the thoracic cardiac nerve to reach the heart because of the topographical relationship of its thoracic origin and the peripheral distributions of the left side of the heart. Therefore, the thoracic cardiac nerve would have to run a complicated course.     

Access of autonomic nerves through the optic canal, and their orbital distribution in man

The notion that autonomic nerves from the internal carotid plexus are transmitted to the orbit with the ophthalmic artery through the optic canal has been variously assumed, disregarded, or denied, but never demonstrated. The objective of this study was to examine the contents of the canal, identify any autonomic nerves, and follow their passage within the orbit. The soft tissues of the optic canal, and the apical tissues of the orbit were removed and examined histologically using 10 cadaver preparations. Additionally, tissues from an orbital exenteration and 10 ocular enucleation or donor specimens were prepared. Some of the latter material was examined with an electron microscope. Numerous autonomic nerves (four to 25, ranging in diameter from 23 to 130 microm) entered the orbit from the internal carotid plexus in the periosteum of the optic canal, the optic nerve dura mater, or the adventitia of the ophthalmic artery. In the orbit they advanced in the loose connective tissue covering the optic nerve dura and joined ciliary nerves close to the eye or entered the eye directly. None were observed to penetrate the dura, apart from a nerve accompanying the central retinal artery. Others were distributed with the ophthalmic artery and its branches. It is concluded that the optic canal is a regular, and often major, route for autonomic nerve distribution to the eye and orbit.