Kaneko Y, Matsuki H, Yoshida K, Sanma S, Ijuin M, Okajima E
Hinyokika Kiyo. 1983 Feb;29(2):207-14.
A case of prepenile scrotum associated with hypospadias and syndactyly is reported. The patient was a full-termed first baby of the 25-year-old mother who had no history of congenital malformation. The clinical laboratory study including chromosomal check and I.V.P. revealed no abnormalities. Two-step operative repair was performed scrotoplasty at 2 years old and urethroplasty at 4 years old. As far as we have reviewed, 18 reports of this malformation have been published in Japan.
本文报告一例阴茎前阴囊合并尿道下裂及并指畸形的病例。该患者为一名25岁母亲的足月头胎婴儿，其母亲无先天性畸形病史。包括染色体检查和静脉肾盂造影在内的临床实验室检查均未发现异常。分两期进行手术修复，2岁时行阴囊成形术，4岁时行尿道成形术。据我们查阅，日本已发表了18例关于这种畸形的报告。
