Sahay Shailesh C, Dogra P N, Rai Pramod K
Department of Urology, All India Institute of medical sciences, New Delhi, India.
Indian J Urol. 2012 Jul;28(3):357-8. doi: 10.4103/0970-1591.102729.
We present the case of a 24 year old man who presented with acute urinary retention and found to have diphallus with vertical duplication of penis. Superior phallus was well developed without any urethral meatus whereas inferior phallus was rudimentary but with patent urethra. History of erection was present in superior phallus only whereas patient was voiding urine from inferior phallus. It was associated with anorectal malformation and bilateral pelvic ectopic kidneys. Patient was managed by suprapubic catheter placement and planned for penile and urethral reconstructive surgery. Diphallus very rarely present in adulthood and vertical duplication is very unusual.
我们报告了一名24岁男性的病例，该患者出现急性尿潴留，经检查发现患有阴茎双体畸形，阴茎呈垂直重复。上方阴茎发育良好，无尿道口，而下方阴茎发育不全，但尿道通畅。只有上方阴茎有勃起功能，而患者通过下方阴茎排尿。该病例伴有肛门直肠畸形和双侧盆腔异位肾。患者接受了耻骨上导管置入治疗，并计划进行阴茎和尿道重建手术。阴茎双体畸形在成年期极为罕见，垂直重复则非常少见。
