O'Donnell Anne-Marie, Puri Prem
National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin 12, Ireland.
Pediatr Surg Int. 2010 Nov;26(11):1065-9. doi: 10.1007/s00383-010-2692-4.
Hirschsprung's disease is characterised by the congenital absence of ganglion cells beginning in the distal rectum and extending proximally for varying distances. 'Zonal aganglionosis' is a phenomenon involving a zone of aganglionosis occurring within normally innervated intestine. 'Skip segment' Hirschsprung's disease (SSHD) involves a 'skip area' of normally ganglionated intestine, surrounded proximally and distally by aganglionosis. While Hirschsprung's disease is believed to be the result of incomplete craniocaudal migration of neural crest-derived cells, the occurrence of SSHD has no clear embryological explanation. The aim of this study was to perform a systematic review of SSHD, reported in the literature between 1954 and 2009, in order to determine the clinical characteristics of this rare entity and its significance.
The first reported case of SSHD was published in 1954. A systematic review of SSHD cases in the literature, from 1954 to 2009, was carried out using the electronic database 'Pubmed'. Detailed information was recorded regarding the age, gender, presenting symptoms and location of the skip segment in each patient.
24 cases of SSHD have been reported in the literature to date. 18/24 (75%) of these cases were males and 6/24 (25%) were females. Of these, 22/24 (92%) were cases of total colonic aganglionosis (TCA), and 2/24 (8%) were rectosigmoid Hirschsprung's disease. Of the 22 TCA cases, 9 (41%) had a skip segment in the transverse colon, 6 (27%) in the ascending colon, 2 (9%) in the caecum and 5 (23%) had multiple skip segments. In both rectosigmoid Hirschsprung's disease cases, the skip segment was in the sigmoid colon. Overall, the length of the skip segment was variable, with the entire transverse colon ganglionated in some cases.
SSHD occurs predominantly in patients with TCA. The existence of a skip area of normally innervated colon in TCA may influence surgical management, enabling surgeons to preserve and use the ganglionated skip area during pull-through operations.
先天性巨结肠症的特征是从直肠远端开始先天性缺乏神经节细胞,并向近端延伸不同距离。“节段性无神经节症”是一种在正常神经支配的肠段内出现无神经节症区域的现象。“跳跃段”先天性巨结肠症(SSHD)涉及一段正常有神经节的肠段(“跳跃区”),其近端和远端均被无神经节症所包围。虽然先天性巨结肠症被认为是神经嵴衍生细胞头尾向迁移不完全的结果,但SSHD的发生尚无明确的胚胎学解释。本研究的目的是对1954年至2009年文献中报道的SSHD进行系统综述,以确定这种罕见疾病的临床特征及其意义。
第一例SSHD病例于1954年发表。使用电子数据库“PubMed”对1954年至2009年文献中的SSHD病例进行系统综述。记录了每位患者的年龄、性别、主要症状和跳跃段的位置等详细信息。
迄今为止文献中已报道24例SSHD。其中18/24(75%)为男性,6/24(25%)为女性。其中,22/24(92%)为全结肠无神经节症(TCA)病例,2/24(8%)为直肠乙状结肠型先天性巨结肠症。在22例TCA病例中,9例(41%)在横结肠有跳跃段,6例(27%)在升结肠,2例(9%)在盲肠,5例(23%)有多个跳跃段。在两例直肠乙状结肠型先天性巨结肠症病例中,跳跃段均在乙状结肠。总体而言,跳跃段的长度各不相同,在某些情况下整个横结肠都有神经节。
SSHD主要发生在TCA患者中。TCA中存在正常神经支配的结肠跳跃区可能会影响手术管理,使外科医生在拖出手术中能够保留并利用有神经节的跳跃区。