结直肠错构瘤表现为会阴肿块的男孩近端尿道下裂。

Pub Date : 2020-01-01 Epub Date: 2020-09-18 DOI:10.1055/s-0040-1715182
Katja P Wolffenbuttel, Cornelius E J Sloots
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引用次数: 1

摘要

先天性会阴病变是罕见的,可与其他出生缺陷如肛门直肠畸形(ARMs)和泌尿生殖器异常一起发生。结直肠错构瘤合并无ARM的泌尿生殖器异常是极为罕见的。我们最近治疗了一个新生儿后尿道下裂和会阴实性肿块,诊断为结直肠错构瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Colorectal Hamartoma Presenting As a Perineal Mass in a Boy with Proximal Hypospadias.

Congenital perineal lesions are rare and can occur along with other birth defects such as anorectal malformations (ARMs) and urogenital anomalies. A colorectal hamartoma associated with a urogenital anomaly without ARM is extremely rare. We recently treated a newborn with posterior hypospadias and a solid perineal mass diagnosed as a colorectal hamartoma.

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