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双阴茎合并异位肠段:一例报告

Diphallus with ectopic bowel segment: a case report.

作者信息

Priyadarshi Shivam

机构信息

Department of Urology, S.M.S. Medical College Hospital, C-80, Gole Market, Jawahar Nagar, Jaipur 302004, India.

出版信息

Pediatr Surg Int. 2005 Aug;21(8):681-3. doi: 10.1007/s00383-005-1441-6. Epub 2005 Oct 13.

Abstract

A 1-year-old boy presented with complete duplication of the penis, with an ectopic bowel segment as an associated anomaly. The boy had duplicated epispadiac urethras. The right one ended blindly whereas the left one was patent, leading into the bladder. There was separation of the symphysis pubis and bifid scrotum. Investigations revealed no other anomalies. A review of the literature concerning diphallus showed a preponderance of associated anomalies such as exstrophy, bladder duplication, ureteral or renal defects, and imperforate anus, but no cases with an ectopic bowel segment. We report this case because of its extreme rarity.

摘要

一名1岁男童出现阴茎完全重复畸形,伴有异位肠段这一相关异常。该男童有重复的尿道上裂尿道。右侧尿道盲端终止,而左侧尿道通畅,通向膀胱。存在耻骨联合分离和阴囊分裂。检查未发现其他异常。关于双阴茎的文献回顾显示,伴有诸如膀胱外翻、膀胱重复畸形、输尿管或肾脏缺陷以及肛门闭锁等相关异常较为常见,但没有伴有异位肠段的病例。我们报告此病例是因其极为罕见。

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