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先天性阴茎尿道皮肤瘘:一种罕见的异常情况及文献综述

Congenital penile urethrocutaneous fistula: A rare anomaly and review of literature.

作者信息

Shukla Ram Mohan, Mukhopadhyay Biswanath, Mandal Kartik Chandra, Barman Shib Sankar

机构信息

Department of Pediatric Surgery, Nil Ratan Sircar Medical College and Hospital, Kolkata, India.

出版信息

Urol Ann. 2011 Sep;3(3):161-3. doi: 10.4103/0974-7796.84953.

DOI:10.4103/0974-7796.84953
PMID:21976932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3183711/
Abstract

Congenital penile urethrocutaneous fistula is described as an unusual developmental anomaly in children who present with an abnormal opening on the ventral aspect of penis with a normal foreskin and an absence of chordee and hypospadias. The authors present a discussion on the etiology, embryology, and management of this entity along with a description of three cases. We emphasize meticulous clinical examination for the diagnosis and to rule out other associated anomalies.

摘要

先天性阴茎尿道皮肤瘘被描述为一种儿童罕见的发育异常,表现为阴茎腹侧有异常开口,包皮正常,无阴茎下弯和尿道下裂。作者对该疾病的病因、胚胎学及治疗进行了讨论,并描述了三例病例。我们强调细致的临床检查对于诊断及排除其他相关异常的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/76ff602b9992/UA-3-161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/10a4e56cfb72/UA-3-161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/2e4f0d4d95b9/UA-3-161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/76ff602b9992/UA-3-161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/10a4e56cfb72/UA-3-161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/2e4f0d4d95b9/UA-3-161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3740/3183711/76ff602b9992/UA-3-161-g003.jpg

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本文引用的文献

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Congenital anterior penile isolated urethrocutaneous fistula: a case report.
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Isolated congenital urethrocutaneous fistula.孤立性先天性尿道皮肤瘘
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