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新生儿先天性巨结肠合并肛门闭锁:罕见关联

Hirschsprung's disease and imperforate anus in a new born: unusual assocation.

作者信息

Mengistu Azene Dessie

机构信息

Felege Hiwot Referal Hospital, Bahir Dar, Ethiopia.

出版信息

Ethiop Med J. 2006 Jan;44(1):81-3.

Abstract

The association of congenital aganglionic megacolon and imperforate anus is rare. Our patient was a male neonate who initially presented with intestinal obstruction due to imperforate anus without fistula. Intraoperative findings and colonic biopsy revealed the presence of concurrent Hirschsprung's disease (HD). A suspicision that these two disorders may coexist is mandatory for early correct diagnosis.

摘要

先天性无神经节细胞巨结肠与肛门闭锁的关联罕见。我们的患者是一名男性新生儿,最初因无瘘管型肛门闭锁出现肠梗阻。术中发现及结肠活检显示同时存在先天性巨结肠(HD)。对于早期正确诊断而言,必须怀疑这两种病症可能并存。

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