Hosomi M, Miyake O, Matsumiya K, Oka T, Takaha M, Kurata A
Department of Urology, Osaka National Hospital.
Hinyokika Kiyo. 1989 Aug;35(8):1431-7.
A 13-year-old Korean boy is reported here as a case of mixed gonadal dysgenesis. The patient presented with perineal hypospadia. He had scrotal testis, epididymis, vas deferens on right side, and abdominal streak gonad, Fallopian tube on left side. He had also uterus and vagina. His chromosome was 46XY type. Among 59 reported cases in Japan, 12 had undergone plasty into male. All of them had hypospadia. In 51 cases, 17 had testes in scrotum. None of them had a testicular tumor. So we decided to do plasty in male, and to follow up his testis quite carefully.
本文报道了一名13岁的韩国男孩,为混合性性腺发育不全病例。该患者表现为会阴型尿道下裂。他右侧有阴囊内睾丸、附睾、输精管,左侧有腹部条索状性腺及输卵管。他还有子宫和阴道。其染色体为46XY型。在日本报道的59例病例中,12例已进行了男性化整形。他们均患有尿道下裂。在51例病例中,17例睾丸位于阴囊内。他们均未患睾丸肿瘤。因此,我们决定为其进行男性化整形,并对其睾丸进行密切随访。