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
相关论文
共 50 条
  • [31] Persistent Mullerian duct syndrome
    Dekker, HM
    de Jong, IJ
    Sanders, J
    Wolf, RFE
    RADIOGRAPHICS, 2003, 23 (02) : 309 - 313
  • [32] Persistent Mullerian duct syndrome
    Rizk, DEE
    Ezimokhai, M
    Hussein, AS
    Gerami, S
    Deb, P
    ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 1998, 261 (02) : 105 - 107
  • [33] Persistent Mullerian Duct Syndrome: 8 New Cases in Southern California and a Review of The Literature
    Salehi, Parisa
    Koh, Chester J.
    Pitukcheewanont, Pisit
    Trinh, Lein
    Daniels, Mark
    Geffner, Mitchell
    PEDIATRIC ENDOCRINOLOGY REVIEWS PER, 2012, 10 (02) : 226 - 233
  • [34] PERSISTENT MULLERIAN DUCT SYNDROME - A CASE-REPORT
    BUSSLINGER, MIC
    KUHLMANN, B
    KAISER, G
    INAEBNIT, D
    ZUPPINGER, K
    EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 : S79 - S79
  • [35] Persistent Mullerian Duct Syndrome: An interesting case report
    Farag, S.
    Sutton, P.
    Leow, K. S.
    Kosai, N. R.
    Razman, J.
    Hanafiah, H.
    Das, S.
    CLINICA TERAPEUTICA, 2013, 164 (04): : 323 - 326
  • [36] US and MRI in a case of persistent Mullerian duct syndrome
    Di Cesare, E
    De Vincentiis, VD
    Maffey, MV
    Splendiani, A
    Masciocchi, C
    PEDIATRIC RADIOLOGY, 1998, 28 (11) : 865 - 867
  • [37] Laparoscopically assisted treatment of transverse testicular ectopia with persistent Mullerian duct syndrome: a case report and review of the literature
    Valioulis, I
    Simaioforidis, V
    Syllas, K.
    HIPPOKRATIA, 2016, 20 (01) : 88 - 89
  • [38] Persistent Mullerian Duct Syndrome Caused by a Novel Mutation of an Anti-Mullerian Hormone Receptor Gene: Case Presentation and Literature Review
    Elias-Assad, Ghadir
    Elias, Marwan
    Kanety, Hannah
    Pressman, Asher
    Tenenbaum-Rakover, Yardena
    PEDIATRIC ENDOCRINOLOGY REVIEWS PER, 2016, 13 (04) : 731 - 740
  • [39] Testicular tumor in a case of, undescended testes, persistent mullerian duct syndrome and transverse testicular ectopia: Report of a case and review of the literature
    Araibi, Haytham
    UROLOGY CASE REPORTS, 2024, 56
  • [40] A rare form of male pseudohermaphroditism-Persistent Mullerian Duct Syndrome
    Ramzan, Raazia
    Khan, Naveed Ali
    Khalique, Abdul
    Aziz, Munira Abdul
    JOURNAL OF SURGICAL CASE REPORTS, 2022, 2022 (12):