RADIOLOGICAL FINDINGS IN 3 CASES OF PERSISTENT MULLERIAN DUCT SYNDROME

被引：22

作者：

ADAMSBAUM, C ^{[1
]}

ROLLAND, Y ^{[1
]}

JOSSO, N ^{[1
]}

KALIFA, G ^{[1
]}

机构：

[1] ECOLE NORM SUPER,INSERM,UNITE RECH ENDOCRINOL DEV,MONTROUGE,FRANCE

来源：

PEDIATRIC RADIOLOGY | 1993年 / 23卷 / 01期

关键词：

D O I：

10.1007/BF02020225

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

We report three cases of persistent Mullerian duct syndrome, which is a rare form of inherited male pseudohermaphroditism characterized by the presence of a uterus and tubes in otherwise normally virilized 46,XY males. We emphasize the usefulness of ultrasonographic study of the pelvis and inguinal areas in the preoperative diagnosis, which is difficult. We recommend that ultrasound be performed routinely in bilaterally cryptorchid patients.

引用

页码：55 / 56

页数：2

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