Carvalho A P, Ramires R, Soares J, Carvalho La Fuente, Filinto M
Servicio de Urologia, Hospital General de Santo António, Oporto, Portugal.
Actas Urol Esp. 2008 Oct;32(9):941-4. doi: 10.1016/s0210-4806(08)73965-2.
Penile duplication is a rare anomaly with an incidence of 1 in 5,500,000. It is almost associated with other malformations like double bladder, presence of the cloaca, imperforate anus, duplication of the recto sigmoid and vertebral deformities. The authors present the surgical technique to resolve a rare case of complete penile duplication in a 4 years old child, without any other malformation.
阴茎重复畸形是一种罕见的异常情况，发病率为1/5500000。它几乎总是与其他畸形相关，如双膀胱、泄殖腔存在、肛门闭锁、直肠乙状结肠重复以及脊柱畸形。作者介绍了一种手术技术，用于解决一名4岁儿童罕见的完全性阴茎重复畸形病例，该患儿无任何其他畸形。
