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Classification of congenital pouch colon based on anatomic morphology

机译:先天性袋状结肠的解剖形态分类

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摘要

Background and aims Congenital pouch colon (CPC) is an extremely rare variant of anorectal malformation (ARM), in which varying lengths of the colon is replaced by a dilated pouch accompanied by a fistula communicating with the genitourinary tract. The aim of this study was to determine the incidence and prevalence of various forms of CPC and to classify it according to anatomic localization of malformation.
机译:背景与目的先天性袋结肠(CPC)是肛门直肠畸形(ARM)的一种极为罕见的变体,其中,不同长度的结肠被扩张的袋所替代,并伴有与泌尿生殖道相通的瘘管。这项研究的目的是确定各种形式的CPC的发生率和患病率,并根据畸形的解剖学位置对其进行分类。

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