脾性腺融合伴持续性苗勒管综合征。
Splenic gonadal fusion with persistent müllerian duct syndrome.
作者信息
Kameoka H, Yamada R, Sonoda T, Okuyama A
机构信息
Department of Urology, Osaka University School of Medicine, Japan.
出版信息
Urol Int. 1993;50(3):170-3. doi: 10.1159/000282477.
PMID:8465485
Abstract
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.
摘要
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。
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