MacKenzie J, Chitayat D, McLorie G, Balfe J W, Pandit P B, Blecher S R
Department of Pediatrics, Hospital for Sick Children, Guelph, Ontario, Canada.
Am J Med Genet. 1994 Jan 1;49(1):103-7. doi: 10.1002/ajmg.1320490120.
We report on a boy born with complete penoscrotal transposition, normal scrotum, twisted penile shaft with hypoplastic penile urethra, meatal stenosis, normal bladder, and bilateral cystic dysplastic kidneys. The patient died of renal failure at 2.5 months. This is the 13th reported case of complete penoscrotal transposition with normal scrotum. The possible pathogenesis is discussed and the literature is reviewed.
我们报告了一名出生时患有完全性阴茎阴囊转位、阴囊正常、阴茎干扭转伴阴茎尿道发育不全、尿道口狭窄、膀胱正常以及双侧多囊性发育不良肾的男婴。该患者在2.5个月时死于肾衰竭。这是第13例报告的伴有正常阴囊的完全性阴茎阴囊转位病例。本文讨论了可能的发病机制并对相关文献进行了综述。
