Gavali J S, Deshpande A V, Sanghani H H, Hirugade S T, Talpallikar M C, Borwankar S S
Department of Paediatric Surgery, Seth G.S. Medical College and K.E.M. Hospital, Parel, Mumbai, Maharashtra 400 012, India.
Pediatr Surg Int. 2002 Jan;18(1):70-1. doi: 10.1007/s003830200018.
An unusual case of a 5-year-old boy with duplication of the glans, a rare variety of diphallia, is reported. The two glandes were arranged one above the other, the dorsal glans had only a blind pit while the ventral glans had a patent urethra with glanular hypospadias. The child also had right renal agenesis and a posterior urethral stricture.
报道了一例5岁男孩阴茎头重复的罕见病例,这是双阴茎的一种罕见类型。两个阴茎头上下排列,背侧阴茎头只有一个盲孔,而腹侧阴茎头有一个开放的尿道并伴有阴茎头型尿道下裂。该患儿还伴有右肾缺如和后尿道狭窄。