Primer cardiac rhabdomyosarcoma: A rare case

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dc.authorscopusid6603461324
dc.authorscopusid55576085900
dc.authorscopusid12762573100
dc.authorscopusid6602622196
dc.contributor.authorOkur F.F.
dc.contributor.authorUyar I.S.
dc.contributor.authorKocatürk H.
dc.contributor.authorÇolak M.C.
dc.date.accessioned2024-08-04T20:02:17Z
dc.date.available2024-08-04T20:02:17Z
dc.date.issued2011
dc.departmentİnönü Üniversitesien_US
dc.description.abstractRhabdomyosarcoma accounts for almost 20% of all primary malignant neoplasms of the heart. Left atrial mass was detected by transthoracic and transesophageal echocardiography, but only histopathology confirmed the nature of the lesion. Although rhabdomyosarcomas of the heart are highly lethal, operation is indicated in order to clarify the diagnosis, relieve symptoms, and improve short-term survival. We report on a case of left atrial rhabdomyosarcoma that required emergency surgery.en_US
dc.identifier.endpage59en_US
dc.identifier.issn1306-8814
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84855449403en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage57en_US
dc.identifier.urihttps://hdl.handle.net/11616/91543
dc.identifier.volume5en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofAnatolian Journal of Clinical Investigationen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectLeft atriumen_US
dc.subjectRhabdomyosarcomaen_US
dc.titlePrimer cardiac rhabdomyosarcoma: A rare caseen_US
dc.title.alternativePrimer kardiyak rabdomyosarkom: Nadir gör?len bir olguen_US
dc.typeArticleen_US

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