持续性苗勒管综合征病例中的超声和磁共振成像
US and MRI in a case of persistent Müllerian duct syndrome.
作者信息
Di Cesare E, Di Bartolo De Vincentiis V, Maffey M V, Splendiani A, Masciocchi C
机构信息
Department of Radiology, University of L'Aquila, Ospedale SM di Collemaggio, I-67 100 L'Aquila, Italy.
出版信息
Pediatr Radiol. 1998 Nov;28(11):865-7. doi: 10.1007/s002470050484.
PMID:9799320
Abstract
We report the US and MR appearances in a case of persistent Müllerian duct syndrome, a rare form of inherited male pseudohermaphroditism characterised by the presence of uterus and fallopian tubes in a normally virilised 46XY male.
摘要
我们报告了一例持续性苗勒管综合征患者的超声和磁共振成像表现，这是一种罕见的遗传性男性假两性畸形，其特征是在正常男性化的46XY男性中存在子宫和输卵管。
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