双阴茎伴直肠肛门畸形病例报告。

Diphallus with anorectal malformation-case report.

机构信息

Department of Paediatric Surgery, B.J. Wadia Hospital for Children, Parel, Mumbai, India.

出版信息

J Pediatr Surg. 2010 Mar;45(3):632-4. doi: 10.1016/j.jpedsurg.2010.01.003.

DOI:10.1016/j.jpedsurg.2010.01.003

PMID:20223333

Abstract

Diphallus is a very rare condition. We report a case of a newborn with absent anal opening and duplication of external genitalia. Examination of the external genitalia showed two well formed penises with fully descended testis within each of the separate hemiscrotums along with soft tissue mass resembling accessory buttock behind the hemiscrotum. Staged reconstruction of duplicated genitalia and anorectal malformation was done. We achieved excellent cosmetic and functional external genitalia.

摘要

双阴茎是一种非常罕见的情况。我们报告了一例新生儿肛门闭锁和外生殖器重复的病例。对外部生殖器的检查显示，两个发育良好的阴茎，每个阴茎都有完全下降的睾丸，位于单独的阴囊内，阴囊后面有类似于附属臀部的软组织肿块。对重复的生殖器和肛门直肠畸形进行了分期重建。我们实现了出色的外生殖器美容和功能。