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结肠三联畸形合并双阴茎及膀胱和尿道完全重复畸形。

Triplication of colon with diphallus and complete duplication of bladder and urethra.

作者信息

Sarin Y K, Manchanda V, Sharma A, Singhal A

机构信息

Department of Pediatric Surgery, Maulana Azad Medical College, New Delhi 110002, India.

出版信息

J Pediatr Surg. 2006 Nov;41(11):1924-6. doi: 10.1016/j.jpedsurg.2006.06.002.

Abstract

Gastrointestinal duplications are a common type of congenital anomaly usually restricted to one part of the gut. Triplication of colon is a rare variation of duplication of the hindgut. Hindgut duplications are commonly associated with anomalies of other derivatives of the cloaca, namely, the lower genitourinary system. Here, we describe a child with triplication of colon with associated duplication of bladder and urethra and diphallus. The child described here is the only reported survivor with triplication.

摘要

胃肠道重复畸形是一种常见的先天性异常,通常局限于肠道的某一部分。结肠重复三联畸形是后肠重复畸形的一种罕见变异。后肠重复畸形通常与泄殖腔其他衍生物的异常有关,即下泌尿生殖系统。在此,我们描述一名患有结肠重复三联畸形并伴有膀胱、尿道重复及双阴茎的患儿。此处描述的患儿是唯一报道的结肠重复三联畸形幸存者。

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