先天性巨结肠症伴全结肠无神经节细胞症和肛门闭锁——病例报告及文献复习。

Hirschsprung disease associated with total colonic agenesis and imperforate anus--case report and review of the literature.

机构信息

Department of Pediatric Surgery, University Childrens Hospital, 72076 Tuebingen, Germany.

出版信息

J Pediatr Surg. 2010 Jan;45(1):252-4. doi: 10.1016/j.jpedsurg.2009.09.036.

DOI:10.1016/j.jpedsurg.2009.09.036

PMID:20105614

Abstract

We report a case of Hirschsprung disease associated with total colonic agenesis and high-type imperforate anus in a newborn girl. The patient also presented with uterus bicornis and a single kidney. The treatment procedure is presented together with a review of literature. The presented combination of pathologies has never been described before.

摘要

我们报告了一例先天性巨结肠症合并全结肠无神经节细胞症和高位肛门闭锁的新生儿病例。该患者还存在双角子宫和单侧肾脏畸形。本文介绍了该病例的治疗经过，并进行了相关文献复习。目前尚未检索到此类多系统先天畸形同时存在的报道。