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Récidive après dix ans de tumeur de granulosa de l’ovaire: à propos de deux cas et revue de la littérature

Granulosa Cell Tumors (GCT) of the ovary are rare tumors belonging to the group of sex cord stromal tumors. They represent 0.6 - 3% of all ovarian tumors and 5% of all malignant tumors. Two different types of GCT can be distinguished: juvenile granulosa cell tumor (JGT) which is characterized by its...

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Detalles Bibliográficos
Autores principales: Majdoul, Soufya, Tawfiq, Nezha, Bourhaleb, Zouhour, Naqos, Nora, Taleb, Amina, Bouchbika, Zineb, Benchakroun, Nadia, Jouhadi, Hassan, Sahraoui, Souha, Benider, Abdelatif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268813/
https://www.ncbi.nlm.nih.gov/pubmed/28154722
http://dx.doi.org/10.11604/pamj.2016.25.30.10433
Descripción
Sumario:Granulosa Cell Tumors (GCT) of the ovary are rare tumors belonging to the group of sex cord stromal tumors. They represent 0.6 - 3% of all ovarian tumors and 5% of all malignant tumors. Two different types of GCT can be distinguished: juvenile granulosa cell tumor (JGT) which is characterized by its aggressive potential and adult granulosa cell tumor (AGT) which is the most common and the least aggressive type. GCT of the ovary usually develops recurrences within 5 years of initial diagnosis but they rarely develop local or peritoneal metastases. Although treatment options including surgery with or without chemotherapy or radiation have been reported in treating GCT relapses, there are no standardized protocols for the treatment of relapses. We here present our therapeutic strategy in the treatment of longterm relapses of GCT peritoneal carcinomatosis occurring in two patients 10 years after the initial diagnosis and a review of the literature.