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一名年轻成人患持续性苗勒管综合征合并多囊卵巢:一例罕见病例报告。

Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report.

作者信息

Hamd Zuhal Y, Ali Muthab A Mohammed, Alorainy Amal I, Gareeballah Awadia, Hamdoun Anas, Manssor E, Alhomida Basim Abdullah

机构信息

Department of Radiological Sciences, College of Health and Rehabilitation Sciences, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.

Department of Medical Diagnostic Ultrasound, Alzaim Alazhari University, Khartoum, Sudan.

出版信息

Radiol Case Rep. 2023 Mar 5;18(5):1825-1829. doi: 10.1016/j.radcr.2023.02.015. eCollection 2023 May.

Abstract

Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudohermaphroditism that occurs in males. It is an autosomal recessive type of familial disease that is commonly associated with a history of consanguinity. We have documented this case of a 22-year-old adult male who came with acute right iliac pain; after an ultrasound scan and hormone investigations, he was diagnosed with polycystic ovarian syndrome (PCOS).

摘要

持续性苗勒管综合征(PMDS)是一种发生于男性的假性两性畸形。它是一种常染色体隐性遗传病,通常与近亲结婚史有关。我们记录了这例22岁成年男性患者,他因急性右下腹疼痛前来就诊;经超声扫描和激素检查后,被诊断为多囊卵巢综合征(PCOS)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5482/10008828/4e0f03a565b4/gr1.jpg

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