Steroid cell tumor of the ovary associated with endometrial adenocarcinoma-a rare case report

dc.contributor.authorAydin, A.
dc.contributor.authorOzkanli, S.
dc.contributor.authorZemheri, E.
dc.contributor.authorGirgin, B.
dc.contributor.authorGuzin, K.
dc.contributor.authorGocmen, A.
dc.date.accessioned2025-05-10T15:24:14Z
dc.date.issued2015
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractEndometrial carcinoma is the most common invasive neoplasm of the female genital tract and is associated to the elevated levels of unopposed estrogen, especially in postmenopause. Ovarian Steroid cell tumors are rare tumors and they are named according to the origin of cell. The most common cancer of the female genital tract is the endometrial adenocarcinoma and it accounts for 7% of all invasive cancers in women. In the present case report, the authors present a 59-year-old multiparous woman with a postmenopausal bleeding complaint and they discuss the case of ovarian steroid cell tumor associated with endometrioid adenocarcinoma of endometrium. Endometrial adenocarcinoma is the most common cancer of female genital tract and its contemporarity with an ovarian steroid cell tumor is extremely rare.
dc.identifier.doi10.12892/ejgo2597.2015
dc.identifier.endpage350
dc.identifier.issn0392-2936
dc.identifier.issue3
dc.identifier.pmid26189269
dc.identifier.scopus2-s2.0-84931067238
dc.identifier.scopusqualityN/A
dc.identifier.startpage348
dc.identifier.urihttps://doi.org/10.12892/ejgo2597.2015
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6648
dc.identifier.volume36
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherS.O.G. CANADA Inc.
dc.relation.ispartofEuropean Journal of Gynaecological Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250302
dc.subjectAdenocarcinoma; Endometrium; Ovary; Steroid cell tumor
dc.titleSteroid cell tumor of the ovary associated with endometrial adenocarcinoma-a rare case report
dc.typeArticle

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