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。
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