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巨尿道:四例报告并文献复习

Megalourethra: a report of four cases and review of the literature.

作者信息

Sharma A K, Shekhawat N S, Agarwal R, Upadhyay A, Mendoza W X, Harjai M M

机构信息

Department of Pediatric Surgery, S.P.M. Child Health Institute, S.M. S. Medical College, Jaipur-302 004, India.

出版信息

Pediatr Surg Int. 1997 Jul;12(5-6):458-60. doi: 10.1007/BF01076969.

Abstract

Megalourethra is a rare congenital anomaly characterized by severe dilatation of the penile urethra. Four cases of congenital megalourethra were seen at Sir Padampat Mother and Child Health Institute, Jaipur, during the last 10 years. Three cases of scaphoid megalourethra had no other associated congenital anomalies and were treat-ed successfully without any complications, while one patient with a fusiform megalourethra had severe associated congenital anomalies and died. These cases are reported with a review of the literature.

摘要

巨尿道是一种罕见的先天性异常,其特征为阴茎尿道严重扩张。在过去10年中,斋浦尔的帕丹帕特母婴健康研究所共收治了4例先天性巨尿道患者。3例舟状巨尿道患者无其他相关先天性异常,治疗成功且无任何并发症,而1例梭形巨尿道患者伴有严重的相关先天性异常并死亡。现报告这些病例并对文献进行综述。

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