Juvenile granulosa cell tumor and high blood Ca-125 levels in children with Pseudo-Meigs syndrome [Juvenile granüloza hücreli tümörü ve Psödo Meig sendromlu çocukda yüksek kan Ca-125 düzeyi]

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dc.contributor.authorCiftci I.
dc.contributor.authorOzgur Pirgon M.
dc.contributor.authorUnlu Y.
dc.date.accessioned2020-03-26T18:44:43Z
dc.date.available2020-03-26T18:44:43Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractOvarian tumors and cysts are rarely seen in children. They constitute 1-2% of solid tumors among children. Over tumors are categorized into three main groups: epithelial, embrionic, and sex cord-stromal tumors. Sex cord-stromal tumors arise from primordial cell cords that are located in the center of the ovary during embriological development. We have detected a patient who was diagnosed with a juvenile granulosa cell tumor (JGCT) at two years of age after presenting with excessive breast enlargement during the past month. She had a large mass in the abdomen, ascites, and marked pleural effusion in the right hemithorax. This association was Pseudo-Meigs syndrome. The association of JGCT and Pseudo-Meigs syndrome is a considerably rare event. Moreover, since the patient was the youngest among all previously reported cases in existing literature, our observations indicate that a juvenile granulosa cell tumor may occur at an early age.In conclusion, Pseudo-Meigs syndrome with JGCT shouldn't forget, even in young children.en_US
dc.identifier.endpage242en_US
dc.identifier.issn1304-3889en_US
dc.identifier.issue4en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage239en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/30040
dc.identifier.volume10en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofEuropean Journal of General Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectCa-125en_US
dc.subjectChilden_US
dc.subjectGranulosa cell tumoren_US
dc.subjectMeigs syndromeen_US
dc.titleJuvenile granulosa cell tumor and high blood Ca-125 levels in children with Pseudo-Meigs syndrome [Juvenile granüloza hücreli tümörü ve Psödo Meig sendromlu çocukda yüksek kan Ca-125 düzeyi]en_US
dc.typeArticleen_US

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