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"Persistent mullerian duct syndrome with ovarian endometriosis- a rare case report."

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dc.contributor.author Savitri Mallikarjun Nerune, Surekha B Hippargi Namrata B Mestri Nikhil M Mehrotra
dc.date.accessioned 2019-11-06T10:58:13Z
dc.date.available 2019-11-06T10:58:13Z
dc.date.issued 2016
dc.identifier.issn 2249782X
dc.identifier.uri http://hdl.handle.net/123456789/1149
dc.description.abstract Persistent Mullerian Duct Syndrome (PMDS) is a rare form of internal male pseudohermaphroditism, characterised by presence of Mullerian duct derivatives in a genotypic and phenotypic male. It is caused by absence of anti- Mullerian hormone or defective functioning of its receptors. We report a case of 19-year-old cryptorchid male with history of orchideopexy who was clinically and radiologically diagnosed as left sided chylocele. A definitive diagnosis of PMDS with ovarian endometriosis was made on histopathological examination which is important for genetic counselling and to reduce complications like infertility and neoplastic transformation. We report this case of PMDS with ovary showing evidence of endometriosis for its rarity. en_US
dc.language.iso en en_US
dc.publisher BLDE(Deemed to be University) en_US
dc.subject Anti-Mullerian hormone, Male pseudohermaphrodite, Orchideopexy en_US
dc.title "Persistent mullerian duct syndrome with ovarian endometriosis- a rare case report." en_US
dc.type Article en_US


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