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持续性苗勒管综合征的MRI表现:一例罕见病例报告

MRI findings of Persistent Mullerian Duct Syndrome: A Rare Case Report.

作者信息

Singh Rambir, Kumar Sunil D, Aggarwal Nidhi

机构信息

Assistant Professor, Department of Radiology, American International Institute of Medical Sciences, Udaipur, Rajasthan, India.

Resident, Department of Radiology, Rnt Medical College, Udaipur, Rajasthan, India.

出版信息

J Clin Diagn Res. 2017 Jun;11(6):TD05-TD06. doi: 10.7860/JCDR/2017/27467.10113. Epub 2017 Jun 1.

Abstract

Embryologically mullerian duct derivatives lead to formation of female genitalia and wolffian duct derivatives to male genitalia. Presence of mullerian duct derivatives in a chromosomally normal male (XY) leads to male pseudohermaphroditism and is referred to as Persistent Mullerian Duct Syndrome (PMDS). A young male patient with bilateral cryptorchidism presented to our hospital who was subsequently imaged. There are many case reports of persistent mullerian duct syndrome but they focus mainly on surgical aspects. In this article, MRI features of persistent müllerian duct syndrome are presented.

摘要

在胚胎学上,苗勒管衍生物导致女性生殖器的形成,而沃尔夫管衍生物导致男性生殖器的形成。染色体正常的男性(XY)体内存在苗勒管衍生物会导致男性假两性畸形,这被称为持续性苗勒管综合征(PMDS)。一名患有双侧隐睾症的年轻男性患者前来我院就诊,随后接受了影像学检查。虽然有许多关于持续性苗勒管综合征的病例报告,但主要集中在手术方面。本文介绍了持续性苗勒管综合征的MRI特征。

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引用本文的文献

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