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先天性前尿道皮肤瘘合并阴茎下弯:一例报告。

Congenital anterior urethrocutaneous fistulas with chordee: A case report.

作者信息

Siregar Safendra, Albert Albert

机构信息

Department of Urology, Hasan Sadikin Hospital, Bandung, West Java 40161, United States of America.

Department of Urology, Hasan Sadikin Hospital, Bandung, West Java 40161, United States of America.

出版信息

Int J Surg Case Rep. 2022 Oct;99:107561. doi: 10.1016/j.ijscr.2022.107561. Epub 2022 Aug 27.

Abstract

Congenital anterior urethrocutanous fistula is a rare genitourinary malformation with unknown etiology and may present as an isolated form or in association with hypospadias or chordee. We describe a case of congenital anterior urethrocutanous fistula with chordee variants in a 5-year-old boy. The patient successfully underwent chordectomy and urethroplasty with no adverse outcomes. We report a review of the literature about the etiology and surgical intervention especially with chordee variants. The congenital anterior urethrocutanous fistula is a rare anomaly with unkown etiopathogenesis.

摘要

先天性前尿道皮肤瘘是一种病因不明的罕见泌尿生殖系统畸形,可单独出现,也可与尿道下裂或阴茎弯曲合并存在。我们描述了一名5岁男孩患有先天性前尿道皮肤瘘合并阴茎弯曲变异的病例。该患者成功接受了阴茎弯曲矫正术和尿道成形术,未出现不良后果。我们报告了一篇关于病因及手术干预尤其是阴茎弯曲变异的文献综述。先天性前尿道皮肤瘘是一种病因发病机制不明的罕见畸形。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef7a/9568707/2c162c025e4c/gr1.jpg

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