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dc.contributor.authorKefeli, Mehmet
dc.contributor.authorBaris, Sancar
dc.contributor.authorAydin, Oguz
dc.contributor.authorYildiz, Levent
dc.contributor.authorYamak, Seda
dc.contributor.authorKandemir, Bedri
dc.date.accessioned2020-06-21T14:17:56Z
dc.date.available2020-06-21T14:17:56Z
dc.date.issued2012
dc.identifier.issn0256-4947
dc.identifier.urihttps://doi.org/10.5144/0256-4947.2012.23.5.1111
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16355
dc.descriptionWOS: 000311585200019en_US
dc.descriptionPubMed: 22634486en_US
dc.description.abstractLeiomyoma is the most common uterine neoplasm. It has several histological variants such as atypical, cellular, myxoid, and epithelioid. Leiomyoma with heterologous elements is a rare variant of leiomyoma, which may contain heterologous elements such as fat, skeletal muscle, and chondroid and osseous tissues. The heterologous sarcomatous differentiation is also rarely seen. We report on a 53-year-old woman who was admitted with abnormal vaginal bleeding and symptoms related to an abdominal mass. She had a huge uterine leiomyoma that contained osteosarcomatous differentiation in several foci. Although malignant progression for leiomyoma is exceedingly rare, when it occurs it may result not only in a leiomyosarcoma but also in a heterologous sarcomatous differention. We have reported histopathological, immunohistochemical, and clinical features of this rare case and reviewed the published studies.en_US
dc.language.isoengen_US
dc.publisherK Faisal Spec Hosp Res Centreen_US
dc.relation.isversionof10.5144/0256-4947.2012.23.5.1111en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleAn unusual case of an osteosarcoma arising in a leiomyoma of the uterusen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume32en_US
dc.identifier.issue5en_US
dc.identifier.startpage544en_US
dc.identifier.endpage546en_US
dc.relation.journalAnnals of Saudi Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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