Suppr超能文献

双阴茎伴尿道重复:一例罕见病例。

Diphallus with urethral duplication: a rare case.

作者信息

Mutlu N, Baykal M, Merder E, Culha M, Canbazoglu N

机构信息

Medical Faculty, Kocaeli University, Turkey.

出版信息

Int J Clin Pract. 1997 Nov-Dec;51(8):525-6.

PMID:9536611
Abstract

We report on a case of glandular diphallus with incomplete urethral duplication associated with rotation anomaly in the right kidney, and a bifid pelvis and an ectopic ureteral orifice in the left kidney. The bladder was single with good sphincter control. At operation, the hipoplasic glans was resected and the urethra which opened into this glans anastomosed alongside the other urethra. Diphallus and incomplete urethral duplication are discussed.

摘要

我们报告一例伴有右肾旋转异常、双叶骨盆和左肾异位输尿管口的腺性双阴茎合并不完全尿道重复畸形病例。膀胱单一,括约肌控制良好。手术时,切除发育不全的龟头,并将开口于该龟头的尿道与另一尿道吻合。对双阴茎和不完全尿道重复畸形进行了讨论。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验