Kameoka H, Yamada R, Sonoda T, Okuyama A
Department of Urology, Osaka University School of Medicine, Japan.
Urol Int. 1993;50(3):170-3. doi: 10.1159/000282477.
Splenic gonadal fusion is a rare anomaly that is frequently associated with skeletal abnormalities or occasionally with cryptorchism. But the case of this anomaly accompanied by male pseudohermaphroditism here represents, to our knowledge, the first report of splenic gonadal fusion with persistent müllerian duct syndrome.
脾性腺融合是一种罕见的异常情况，常与骨骼异常相关，偶尔也与隐睾症有关。但据我们所知，此处这种伴有男性假两性畸形的异常情况代表了首例伴有持续性苗勒管综合征的脾性腺融合报告。
