Kobayashi Hiroyuki, Yamataka Atsuyuki, Lane Geoffrey J, Miyano Takeshi
Department of Pediatric Surgery, Juntendo University School of Medicine, Tokyo, Japan.
J Pediatr Surg. 2004 Feb;39(2):152-6; discussion 152-6. doi: 10.1016/j.jpedsurg.2003.10.008.
The aim of this study was to clarify the pathogenesis of intestinal neuronal dysplasia (IND).
The bowel habits of 36 postoperative HD patients were assessed retrospectively. Twenty-five had no complaints. Seven had persistent enterocolitis and were the focus of our study. They were divided into group A (n = 2) if they were severe and had associated postoperative surgical complications, and group B (n = 5) if they were mild. The histological changes were assessed.
The 7 patients who had persistent enterocolitis postoperatively had no AchE activity in the mucosa, and there was normal distribution of submucosal and myenteric ganglia in the proximal resection margin. Rectal biopsies performed postoperatively for investigation of persistent enterocolitis in group A showed inflammatory changes and typical histopathologic features of IND such as abundant acetylcholinesterase (AchE)-positive nerve fibers in the lamina propria associated with giant submucosal ganglia and hyperganglionosis, and in group B there was increased AchE activity without hyperganglionosis or giant ganglia.
This is the first report of histopathologic changes typical of IND occurring in response to persistent enterocolitis related to postoperative complications of surgery for HD.
本研究旨在阐明肠道神经元发育异常(IND)的发病机制。
回顾性评估36例术后先天性巨结肠(HD)患者的排便习惯。25例无不适主诉。7例患有持续性小肠结肠炎,是我们研究的重点。若病情严重且伴有术后手术并发症,则分为A组(n = 2);若病情较轻,则分为B组(n = 5)。评估组织学变化。
术后患有持续性小肠结肠炎的7例患者黏膜中无乙酰胆碱酯酶(AchE)活性,近端切除边缘黏膜下和肌间神经节分布正常。为调查A组持续性小肠结肠炎而在术后进行的直肠活检显示有炎症变化以及IND的典型组织病理学特征,如固有层中大量乙酰胆碱酯酶(AchE)阳性神经纤维伴巨大黏膜下神经节和神经节增生,而B组AchE活性增加,但无神经节增生或巨大神经节。
这是首次报道与HD手术术后并发症相关的持续性小肠结肠炎引发的IND典型组织病理学变化。