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1
Case report: congenital urethrocutaneous fistula.病例报告：先天性尿道皮肤瘘
J Anat. 1997 Jan;190 ( Pt 1)(Pt 1):155-6. doi: 10.1046/j.1469-7580.1997.19010155.x.
2
Congenital urethrocutaneous fistula: a case report and literature review, with a nomenclature proposal.先天性尿道皮肤瘘：一例病例报告及文献综述，并提出命名建议。
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3
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引用本文的文献

1
Congenital anterior urethrocutaneous fistula: A systematic review.先天性前尿道皮肤瘘：一项系统综述。
Afr J Paediatr Surg. 2018 Apr-Jun;15(2):63-68. doi: 10.4103/ajps.AJPS_97_17.
2
A congenital anterior urethrocutaneous fistula in a boy whose mother was exposed to ionizing radiations: case report and literature review.一名母亲曾暴露于电离辐射下的男孩患先天性前尿道皮肤瘘：病例报告及文献综述
Case Rep Urol. 2013;2013:525386. doi: 10.1155/2013/525386. Epub 2013 Feb 26.

病例报告：先天性尿道皮肤瘘

Case report: congenital urethrocutaneous fistula.

作者信息

Barwell J, Harris D

出版信息

J Anat. 1997 Jan;190 ( Pt 1)(Pt 1):155-6. doi: 10.1046/j.1469-7580.1997.19010155.x.

DOI:10.1046/j.1469-7580.1997.19010155.x
PMID:9034892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1467594/
Abstract

A 2-year-old boy presented with a suspected urethrocutaneous fistula. He had been born at 26 wk gestation and spent 14 wk in the special care baby unit with severe respiratory problems and an episode of meningitis. He had not had a urinary catheter in situ or urinary tract infections. Bilateral inguinal hernias had been repaired. At presentation he was below the 3rd centile for height and weight but had reached all other developmental milestones.

摘要

一名2岁男孩因疑似尿道皮肤瘘前来就诊。他在孕26周时出生，因严重呼吸问题和一次脑膜炎发作在特殊护理婴儿病房住了14周。他未曾留置过导尿管，也没有尿路感染史。双侧腹股沟疝已修复。就诊时，他的身高和体重低于第3百分位，但已达到所有其他发育里程碑。