结肠闭锁伴肛门直肠畸形--罕见病例报告及文献综述

Ashoka Nand Thakur, Ankita Sharma
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引用次数: 0

摘要

结肠闭锁是一种罕见的肠道闭锁,每 20000 名活产婴儿中约有 1 例。[1]它可能表现为孤立的病变,也可能伴有其他先天性畸形,如赫氏病(hirschsprung'sdisease)、无孔肛门(imperforate anus)、外颅畸形(exomphalos)、多发性闭锁(multiple atresia)或结肠重复(colonic duplication)。当结肠闭锁伴有其他先天性畸形时,诊断难度很大。我们在此介绍一例肛门穿孔患者,他们是在外科医生的帮助下进行肛门修。闭锁的远端距脱垂部分约 ve 厘米。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COLONIC ATRESIA WITH ANORECTAL MALFORMATION — A RARE CASE REPORT WITH REVIEW OF LITERATURE
Colonic atresia is a rare form of intestinal atresia accounts for around 1 per 20000 live births. [1] It may present as isolated lesion or it may be associated with other congenital anomalies like hirschsprung's disease, imperforate anus, exomphalos, multiple atresia or colonic duplication. This is quite difcult to make diagnosis when colonic atresia is associated with other congenital anomalies. We are presenting a case of imperforate anus operated outside came to us for denitive repair. The distal atretic segment was about ve cm from prolapsed part.
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