Sertoli-Leydig Cell -A Rare Male Hormone Producing Ovarian Tumor

Khalida Nasreen; Rozina Mustafa

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dc.contributor.author	Khalida Nasreen
dc.contributor.author	Rozina Mustafa
dc.date.accessioned	2018-12-06T08:00:15Z
dc.date.available	2018-12-06T08:00:15Z
dc.date.issued	2013-01-01
dc.identifier.issn	2220-7562
dc.identifier.uri	http://hdl.handle.net/123456789/7950
dc.description.abstract	Sertoli-Leydig cell tumor (SLCT) of ovary is an unusual neoplasm that belongs to a group of sex cord-stromal tumors of ovary. It accounts for less than 0.5% of all primary ovarian neoplasms. We report a case of primary intermediate ovarian Sertoli-Leydig cell tumor (SLCT) involving the left ovary in a 32-year-old nulliparous woman who presented with history of secondary amenorrhea for 8 months, hirsutism, and voice changes.	en_US
dc.description.sponsorship	JBUMDC	en_US
dc.language.iso	en	en_US
dc.publisher	Bahria University Medical and Dental College Karachi	en_US
dc.relation.ispartofseries	3;1
dc.subject	Sertoli-leydig cell tumor, ovarian tumor, secondary amenorrhea.	en_US
dc.title	Sertoli-Leydig Cell -A Rare Male Hormone Producing Ovarian Tumor	en_US
dc.type	Article	en_US