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一名患有近端尿道下裂的男孩,以会阴肿物形式出现的大肠错构瘤

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

作者信息

Wolffenbuttel Katja P, Sloots Cornelius E J

机构信息

Department of Urology and Pediatric Urology, Erasmus MC Sophia, Rotterdam, The Netherlands.

Department of Pediatric Surgery, Erasmus MC Sophia, Rotterdam, The Netherlands.

出版信息

European J Pediatr Surg Rep. 2020 Jan;8(1):e71-e74. doi: 10.1055/s-0040-1715182. Epub 2020 Sep 18.

Abstract

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.

摘要

先天性会阴病变较为罕见,可与其他出生缺陷同时出现,如肛门直肠畸形(ARM)和泌尿生殖系统异常。与无ARM的泌尿生殖系统异常相关的结直肠错构瘤极为罕见。我们最近治疗了一名患有后尿道下裂和实性会阴肿物的新生儿,该肿物被诊断为结直肠错构瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bad/7500975/8ba195244d5d/10-1055-s-0040-1715182-i200524cr-1.jpg

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