真性完全性双阴茎畸形
True complete diphallia.
作者信息
Zolfaghari A, Pourissa M, Hajialilou S, Amjadi M
机构信息
Department of Urology, Medical Sciences University of Tabriz, Iran.
出版信息
Scand J Urol Nephrol. 1995 Jun;29(2):233-5. doi: 10.3109/00365599509180570.
PMID:7569806
Abstract
In a case of true complete diphallia, the orthotopic penis was normal in length, shape and urethra, whereas the ectopic, perianal, penis had a blind-ending urethra, the significant distance between the two making the malformation of an extremely rare type. Right renal agenesis and orthopaedic malformations were also present.
摘要
在一例真正的完全性双阴茎病例中，原位阴茎在长度、形状和尿道方面均正常，而异位的肛周阴茎有一个盲端尿道，两者之间的显著距离使得这种畸形极为罕见。同时还存在右肾缺如和骨科畸形。
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