Adult-type granulosa cell tumor with splenic metastasis: a rare case

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dc.authorid0000-0001-6768-1275
dc.authorid0000-0002-2507-0238
dc.authorid0000-0003-4096-4261
dc.contributor.authorDüzcü, Selma Erdoğan
dc.contributor.authorTunç, Nur
dc.contributor.authorBoran, Çetin
dc.date.accessioned2021-06-23T19:54:40Z
dc.date.available2021-06-23T19:54:40Z
dc.date.issued2020
dc.departmentBAİBÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.description.abstractTo the Editor, Granulosa cell tumors are rare malignant tumors defined by Rokitansky in 1855 and consist 2-3% of all ovarian tumors1. Incidence rate is 0.5-1.5/100.000 cases per year2. Characteristically it grows very slowly yet metastasizes years later after the curative tratment 1. The mean age is 50 years but it can be seen at any age after the menopause and patients admit to the clinics with complaints of uterine bleeding, pain and symptoms secondary to pressure2,3. A case with splenic metastasis after three years of the diagnosis of adult-type granulosa cell tumoen_US
dc.identifier.endpage1853en_US
dc.identifier.issn2602-3032
dc.identifier.issn2602-3040
dc.identifier.issue4en_US
dc.identifier.startpage1850en_US
dc.identifier.trdizinid1115845en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12491/10612
dc.identifier.urihttps://dergipark.org.tr/tr/download/article-file/1264748
dc.identifier.volume45en_US
dc.identifier.wosWOS:000609003200070en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.institutionauthorDüzcü, Selma Erdoğan
dc.institutionauthorTunç, Nur
dc.institutionauthorBoran, Çetin
dc.language.isoenen_US
dc.publisherCukurova Univ, Fac Medicineen_US
dc.relation.ispartofCukurova Medical Journalen_US
dc.relation.publicationcategoryEditöre Mektup - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAdult-type Granulosa Cell Tumoren_US
dc.titleAdult-type granulosa cell tumor with splenic metastasis: a rare caseen_US
dc.title.alternativeDalak metastazı gösteren erişkin tip granuloza hücreli tümör: nadir bir olguen_US
dc.typeLetteren_US

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