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直肠泌尿会阴瘘——一种独特的异常情况。

Rectourinary perineal fistula--a unique anomaly.

作者信息

Chatterjee Subir K, Basu Ashoke K, Chatterjee Uday Sankar

机构信息

Park Children's Center for Treatment and Research, 700017 Kolkata, India.

出版信息

J Pediatr Surg. 2005 Oct;40(10):1658-61. doi: 10.1016/j.jpedsurg.2005.06.009.

DOI:10.1016/j.jpedsurg.2005.06.009
PMID:16227003
Abstract

Two patients who presented with a unique anorectal malformation are described. They had what we have named rectourinary perineal fistula. The first patient had a more severe malformation, rectovesicoperineal fistula, and has been followed up for 28 years. The second, with a lesser malformation, rectourethroperineal fistula, has been followed up for 19 years.

摘要

本文描述了两名患有独特肛门直肠畸形的患者。他们患有我们命名的直肠泌尿会阴瘘。第一名患者畸形更为严重,为直肠膀胱会阴瘘,已随访28年。第二名患者畸形较轻,为直肠尿道会阴瘘,已随访19年。

相似文献

1
Rectourinary perineal fistula--a unique anomaly.直肠泌尿会阴瘘——一种独特的异常情况。
J Pediatr Surg. 2005 Oct;40(10):1658-61. doi: 10.1016/j.jpedsurg.2005.06.009.
2
[Incomplete duplication of the urethra with intra-rectal opening of the posterior chanel (author's transl)].尿道不完全重复伴后通道直肠内开口(作者译)
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[Congenital entero-urinary fistulas].
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[Exstrophy of rectal duplication associated with anorectal malformation and penoscrotal transposition with perineal hypospadias. A case report].[直肠重复畸形外翻合并肛门直肠畸形及阴茎阴囊转位伴会阴型尿道下裂。病例报告]
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[Complete duplication of the urethra and bladder].
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Laparoscopic management of congenital H-type urethroanal fistula.先天性H型尿道肛门瘘的腹腔镜治疗
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J Urol (Paris). 1980;86(9):681-3.
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Rectourethroperineal Fistula Associated with an Atretic Bulbomembranous Urethra: Successful Staged Management of a New Variant of an Extremely Rare Anorectal Malformation.与闭锁性球膜部尿道相关的直肠尿道会阴瘘:一种极其罕见的肛门直肠畸形新变体的成功分期治疗
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Cloaca-Like Anomalies in the Male: A Report on Two Cases.
男性泄殖腔样畸形:两例报告
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Cloacal malformation variants in male.男性泄殖腔畸形变体
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