Article ID Journal Published Year Pages File Type
3968508 Progresos de Obstetricia y Ginecología 2015 4 Pages PDF
Abstract

ResumenLos tumores de Sertoli-Leydig son un tipo infrecuente de tumor de ovario de estirpe no epitelial; concretamente, pertenecen al grupo de los tumores de los cordones sexuales-estroma, con una incidencia aproximada de un 2-5% de todas las neoplasias ováricas malignas.Presentamos el caso de una paciente de 42 años intervenida de un tumor de Sertoli con focos sarcomatoides. El diagnóstico de estos tumores es difícil de establecer prequirúrgicamente, y debido a la escasez de publicaciones, existe mucha controversia acerca de la estadificación quirúrgica idónea y sobre la conveniencia de realizar o no tratamiento adyuvante.

Sertoli-Leydig cell tumors are a rare type of non-epithelial ovarian cancer; these tumors belong to the group of sex cord-stromal tumors and account for approximately 2-5% of all malignant ovarian tumors.We report the case of a 42-year-old woman who underwent surgery for a Sertoli tumor with sarcomatoid foci. Diagnosis of these tumors is difficult before surgery and, due to the scarcity of publications on the topic, there is controversy about the appropriate surgical staging and the role of adjuvant therapy in the management of this entity.

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Health Sciences Medicine and Dentistry Obstetrics, Gynecology and Women's Health
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