A Rare Case of Persistent Mullerian Duct Syndrome and Review of Literature

被引:4
|
作者
Ahadi, Mahsa [1 ,2 ]
Soleimantabar, Hussein [3 ]
Javanmard, Babak [4 ,5 ]
Zahedifard, Sara [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Canc Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Fac Med, Dept Pathol, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Imam Hussein Hosp, Fac Med, Dept Radiol, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, LAMSRC, Tehran, Iran
[5] Shahid Beheshti Univ Med Sci, Shohada E Tajrish Hosp, Dept Urol, Tehran, Iran
关键词
Anti-Mullerian Hormone; Cryptorchidism; Persistent Mullerian Duct Syndrome; MIILLERIAN DUCT;
D O I
10.5812/ijcm.99102
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Persistent Mullerian duct syndrome (PMDS) is a scarce type of male pseudohermaphroditism due to anti-Mullerian hormone dysfunction. So, Mullerian duct derivatives such as the uterus, cervix, fallopian tubes, and two-thirds of the vagina are seen in a normal phenotypic and genotypic male. Considering and assessing the clinical manifestations, associated diseases, histopathology, and imaging findings can be clues in the management of such cases. Case Presentation: Here, we describe a case of PMDS with left inguinal hernia and bilateral cryptorchidism and discuss the management and review of the literature. Also, the case has a history of brain mass with a pathologic diagnosis of ganglioneuroma. Is there a correlation between PMDS and extragenital neoplasm? it needs more investigation in the future. Conclusions: Bilateral cryptorchidism could provide us with a hint toward PMDS diagnosis. However, genetic counseling will be required, particularly in parental consanguinity.
引用
收藏
页数:6
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