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儿童完全性尿道重复畸形：一例报告

Complete Urethral Duplication in Children: A Case Report.

作者信息

Roshanzamir Fatollah, Mirshemirani Alireza, Ghoroubi Javad, Mahdavi Alireza, Mohajerzadeh Leily, Sarafi Mehdi

机构信息

Pediatric Surgery Research Center, Shahid Beheshti University of Medial Sciences, Tehran, IR Iran.

Department of Pediatric Anesthesiology, Shahid Beheshti University of Medial Sciences, Tehran, IR Iran.

出版信息

Iran J Pediatr. 2016 Mar 5;26(2):e3620. doi: 10.5812/ijp.3620. eCollection 2016 Apr.

DOI:10.5812/ijp.3620
PMID:27307964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4906148/
Abstract

INTRODUCTION

Urethral duplication (UD) is a rare congenital anomaly with multiple anatomical variants.

CASE PRESENTATION

In this article we present a four year-old child with complete UD. The patient was admitted for hypospadias repair, in evaluation we found type IIA1 UD according to Effmann classification. Patient underwent hypospadias repair saving complete UD.

CONCLUSIONS

After one year follow-up he has normal and continent urination.

摘要

引言

尿道重复畸形（UD）是一种罕见的先天性异常，具有多种解剖学变异。

病例报告

在本文中，我们介绍了一名患有完全性UD的4岁儿童。该患者因尿道下裂修复入院，在评估中我们根据埃夫曼分类法发现为IIA1型UD。患者接受了尿道下裂修复术，同时保留了完整的UD。

结论

经过一年的随访，他排尿正常且能自主控制排尿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/32779cc86486/ijp-26-02-3620-i004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/46cff43a5a48/ijp-26-02-3620-i001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/d0acb59458f7/ijp-26-02-3620-i002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/96602e8e0764/ijp-26-02-3620-i003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/32779cc86486/ijp-26-02-3620-i004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/46cff43a5a48/ijp-26-02-3620-i001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/d0acb59458f7/ijp-26-02-3620-i002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/96602e8e0764/ijp-26-02-3620-i003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7281/4906148/32779cc86486/ijp-26-02-3620-i004.jpg

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本文引用的文献

1
Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly.伴有尿道重复的腺体双阴茎：一种罕见先天性异常的传统治疗技术。
Indian J Urol. 2015 Oct-Dec;31(4):369-71. doi: 10.4103/0970-1591.166458.
2
Urethral duplication: a rare cause of recurrent urinary infection.尿道重复畸形：复发性尿路感染的罕见病因。
J Pak Med Assoc. 2015 Jan;65(1):90-2.
3
Urethral duplication in a 15-year-old: case report with review of the literature.一名15岁男性的尿道重复畸形：病例报告并文献复习
Rev Urol. 2014;16(3):149-51.
4
Urethral duplication in a 12-year-old child.一名12岁儿童的尿道重复畸形。
Afr J Paediatr Surg. 2011 Sep-Dec;8(3):313-6. doi: 10.4103/0189-6725.91667.
5
Urethral duplication in children: our experience of eight cases.儿童尿道重复畸形：我们的8例经验
J Pediatr Urol. 2009 Oct;5(5):363-7. doi: 10.1016/j.jpurol.2009.01.006. Epub 2009 Feb 23.
6
Urethral duplication in males: our experience in ten cases.男性尿道重复畸形：我们的10例经验
Pediatr Surg Int. 2007 Aug;23(8):789-94. doi: 10.1007/s00383-007-1967-x. Epub 2007 Jun 19.
7
Y-type urethral duplication in the male.男性Y型重复尿道
BJU Int. 2006 Mar;97(3):597-602. doi: 10.1111/j.1464-410X.2006.06025.x.
8
A new case of male Y-type urethral duplication and review of literature.男性Y型重复尿道一例并文献复习
J Pediatr Surg. 2006 Jan;41(1):e69-71. doi: 10.1016/j.jpedsurg.2005.10.084.
9
Complete duplication of urinary bladder and urethra: prenatal sonographic features.膀胱和尿道完全重复畸形：产前超声特征
Ultrasound Obstet Gynecol. 2004 Sep;24(4):464-6. doi: 10.1002/uog.1093.
10
[Urethral sagittal duplication in children. Report of 7 cases].[儿童尿道矢状面重复畸形。7例报告]
Prog Urol. 2002 Feb;12(1):77-83.