Hutson J M, Chow C W, Borg J
F. Douglas Stephens Surgical Research Unit, Royal Children's Hospital, Melbourne, Australia.
J Pediatr Surg. 1996 Apr;31(4):580-3. doi: 10.1016/s0022-3468(96)90501-1.
After Hirschsprung's disease was ruled out for 25 children who had severe chronic constipation, the authors studied the distribution of immunoreactivity for substance P (SP) and vasoactive intestinal peptide (VIP) in the intestinal wall, using immunofluorescence. SP and VIP immunoreactivity identify excitatory and inhibitory nerve fibres, respectively. Full-thickness rectal biopsy specimens were unsatisfactory, so seromuscular biopsies of the caecum, transverse colon, and sigmoid colon were obtained (by laparoscopy and laparotomy; n = 10 patients). SP-immunoreactive fibres were markedly reduced in seven, with concomitant reduction of VIP-immunoreactive fibres in four. In two other patients, there was no obvious reduction in SP- or VIP-immunoreactive fibres. In a patient who subsequently was found to have multiple endocrine neoplasia type 2b, the myenteric plexus was markedly hyperplastic, with an increase in nerve cells and nerve fibres. VIP-immunoreactive fibres were increased, but SP-immunoreactive fibres were markedly decreased. Surgical options included proximal stoma, Malone operation, and subtotal colectomy with preservation of the rectum. Three children with subtotal colectomy have had improvement over short-term follow-up. The combination of seromuscular laparoscopic biopsies and immunofluorescence demonstration of neuropeptides may identify new variants of intestinal neuronal dysplasia than can be treated successfully with surgery.
在排除了25例患有严重慢性便秘儿童的先天性巨结肠病后,作者采用免疫荧光法研究了肠壁中P物质(SP)和血管活性肠肽(VIP)的免疫反应性分布。SP和VIP免疫反应性分别识别兴奋性和抑制性神经纤维。全层直肠活检标本不理想,因此获取了盲肠、横结肠和乙状结肠的浆肌层活检标本(通过腹腔镜检查和剖腹手术;n = 10例患者)。7例患者的SP免疫反应性纤维明显减少,其中4例患者的VIP免疫反应性纤维也随之减少。另外2例患者的SP或VIP免疫反应性纤维没有明显减少。在1例随后被发现患有2b型多发性内分泌腺瘤的患者中,肌间神经丛明显增生,神经细胞和神经纤维增多。VIP免疫反应性纤维增加,但SP免疫反应性纤维明显减少。手术选择包括近端造口术、马龙手术以及保留直肠的结肠次全切除术。3例接受结肠次全切除术的儿童在短期随访中病情有所改善。浆肌层腹腔镜活检与神经肽免疫荧光显示相结合,可能会识别出可通过手术成功治疗的肠道神经元发育异常的新变体。