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Sex Cord-Stromal Ovarian Tumors is a topic covered in the Pediatric Surgery NaT.

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Sex cord-stromal tumors account for 5.7 to 17% of malignant tumors in series of ovarian neoplasms in children [1]. They arise from uncommitted mesenchymal stem cells that reside below the surface epithelium of the urogenital ridge [2][3]. This totipotential tissue has the potential to differentiate into several different cell lines including granulosa-theca cells in the ovary and the Sertoli-Leydig cells in the testicular interstitium. Sex cord-stromal tumors are referred to as functioning ovarian tumors as they have systemic hormonal effects. Before nine years of age, most sex cord-stromal tumors are feminizing. After nine years of age there is a predominance of virilizing neoplasms [4].

see also Ovarian Tumors

Content in these topics is referenced in SCORE Ovarian and Adnexal Problems overview

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Last updated: August 21, 2017


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TY - ELEC T1 - Sex Cord-Stromal Ovarian Tumors ID - 829128 A1 - Burnweit,Cathy,MD AU - Fallat,Mary,MD AU - von Allmen,Daniel,MD ED - Hirschl,Ron, ED - Powell,David, ED - Waldhausen,John, Y1 - 2017/08/21/ BT - Pediatric Surgery NaT UR - https://www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829128/all/Sex_Cord_Stromal_Ovarian_Tumors PB - American Pediatric Surgical Association DB - APSA Webapp DP - Unbound Medicine ER -