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儿童胃肠动力障碍的组织病理学

The histopathology of gastrointestinal motility disorders in children.

作者信息

Feichter Sonja, Meier-Ruge William A, Bruder Elisabeth

机构信息

Department of Pediatric Surgery, Hospital Lucerne, Lucerne, Switzerland.

出版信息

Semin Pediatr Surg. 2009 Nov;18(4):206-11. doi: 10.1053/j.sempedsurg.2009.07.002.

Abstract

Gastrointestinal motility disorders and chronic constipation are common pediatric problems. Symptoms of abdominal discomfort are frequently encountered in the daily practice of pediatricians and pediatric surgeons. Normal peristalsis depends on the interaction between muscles, nerve cells, and tendinous connective tissue of muscularis propria. Malfunction of any of these components results in a motility disorder. Aganglionosis, typically of the left distal colon, is the cause of Hirschsprung disease. Hypoganglionosis constitutes another gastrointestinal motility disorder. In hypoplastic hypoganglionosis, the number of nerve cells and the size of ganglia of the enteric nervous system are reduced, resulting in symptoms similar to aganglionosis. In intestinal neuronal dysplasia type B, submucous plexus development is disturbed. Immaturity of the enteric nervous system, but also ganglioneuromatosis, can be the underlying cause of chronic constipation. Chronic constipation may be caused by a myopathy. Aplasia or atrophy of the tendinous connective tissue of muscularis propria may cause desmosis, which may result in an aperistaltic syndrome. In severe chronic constipation, a histopathological diagnosis of the underlying cause is useful. In the diagnostic approach for most of these causes of chronic constipation, enzyme histochemistry is an efficient tool to complement conventional immunohistochemical and selected molecular technologies. An interdisciplinary approach of a gastrointestinal working group is beneficial in the management of these difficult patients.

摘要

胃肠动力障碍和慢性便秘是常见的儿科问题。腹部不适症状在儿科医生和小儿外科医生的日常诊疗中经常遇到。正常蠕动依赖于固有肌层的肌肉、神经细胞和腱性结缔组织之间的相互作用。这些组成部分中的任何一个出现故障都会导致动力障碍。神经节缺如,通常发生在左半结肠远端,是先天性巨结肠病的病因。神经节减少症是另一种胃肠动力障碍。在发育不全性神经节减少症中,肠神经系统的神经细胞数量和神经节大小减少,导致与神经节缺如相似的症状。在B型肠道神经元发育异常中,黏膜下神经丛发育受到干扰。肠神经系统不成熟以及神经节瘤病都可能是慢性便秘的潜在原因。慢性便秘可能由肌病引起。固有肌层腱性结缔组织发育不全或萎缩可能导致腱膜病,进而可能导致无蠕动综合征。在严重慢性便秘中,对潜在病因进行组织病理学诊断很有用。在诊断大多数这些慢性便秘病因时,酶组织化学是补充传统免疫组织化学和特定分子技术的有效工具。胃肠工作组的多学科方法有助于管理这些难治性患者。

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