Persistent Müllerian Ducts Syndrome: A Case Report

International Journal of Medical Science
© 2019 by SSRG - IJMS Journal
Volume 6 Issue 4
Year of Publication : 2019
Authors : Hadeel A. Yasseen, Mahdi A Hama, Ghasak Ghazi Faisal
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How to Cite?

Hadeel A. Yasseen, Mahdi A Hama, Ghasak Ghazi Faisal, "Persistent Müllerian Ducts Syndrome: A Case Report," SSRG International Journal of Medical Science, vol. 6,  no. 4, pp. 1-3, 2019. Crossref, https://doi.org/10.14445/23939117/IJMS-V6I4P101

Abstract:

Persistent mullerian duct syndrome (PMDS) is usually an accidental finding during routine inguinal hernia repair in male patients. Intraoperatively, mullerian remnants consisting of an infantile uterus and fallopian tubes are usually found. Herein we report a case of PMDS in a 3-year-old boy presenting with unilateral undescended testes.The right testis was not palpable and the diagnostic ultrasound shows a non-visualized right testis neither in scrotum nor in the right inguinal region.

Keywords:

Persistent mullerian duct syndrome, Hernia uteri inguinale, anti-mullerian hormone, cryptorchidism.

References:

[1] R. Payan-Carreira, M. A. Pires and J. Robalo Silva. Sex Chromosomes: Genetics, Abnormalities, and Disorders. XY Male Pseudohermaphroditism, 2009, chapter 9, Editor: C. N. Weingarten and S. E. Jefferson, Nova Science Publishers Inc: pp 165-190
[2] Miller A, Hong MK, Hutson JM: The broad ligament: a review of its anatomy and development in different species and hormonal environments. ClinAnat.2004;17: 244–251.
[3] Robboy SJ, Bentley RC, Russell P, Anderson P. Fox H, Wells M. Haines and Taylor-Obstetrical and Gynecological Pathology. 5th ed. United Kingdom: Churchill Livingstone Elsevier; 2003. Pathology of abnormal sexual development; pp. 1209–32.
[4] Jean-Yves Picard a–c Richard L. Cate d Chrystèle Racine a–c Nathalie Josso. The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases. Sex Dev 2017;11:109–125
[5] Belville C, Josso N, Picard JY. (1999). Persistence of Müllerian derivatives in males. Am J Med Genet. 89,218-23.
[6] Hunter RHF. (1995). Sex Determination Differentiation and Intersexuality in PlacentalMammals. Cambridge University Press, Cambridge, pp. 310.
[7] Josso N, Belville C, di Clemente N, Picard JY. (2005). AMH and AMH receptor defects in persistent Müllerian duct syndrome. Hum Reprod Update. 11,351-6.
[8] Abduljabbar M, Taheini K, Picard JY, Cate RL, Josso N: Mutations of the AMH type II receptor in two extended families with persistent Mullerian duct syndrome: lack of phenotype/ genotype correlation. Horm Res Paediatr.2012;77: 291–297
[9] Manjunath BG, Shenoy VG, Raj P. Persistent müllerian duct syndrome: How to deal with the müllerian duct remnants- A review. Indian J Surg. 2010;72:16–9. [PMC free article] [PubMed]
[10] Farag TI: Familial persistent Mullerian duct syndrome in Kuwait and neighboring populations. Amer J Med Genet.1993;47: 432–434.
[11] Modi J, Modi D, Bachani L: Acute urinary retention caused by seminoma in a case of persistent Mullerian duct syndrome. Indian J PatholMicrobiol. 2015;58: 83–85.