Rhabdomyosarcoma in an adult hand

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dc.contributor.authorSeyhan, Nevra
dc.contributor.authorKeskin, Mustafa
dc.contributor.authorTosun, Zekeriya
dc.contributor.authorSavaci, Nedim
dc.date.accessioned2020-03-26T18:43:13Z
dc.date.available2020-03-26T18:43:13Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractRhabdomyosarcoma (RMS) is a malign tumour which arises from cells committed to a skeletal muscle lineage. It constitutes 4%-8% of all childhood malignancies but is rare in adults. The rare pleomorphic subtype occurs almost exclusively in adults and most often involves the extremities. RMS of the hand or foot comprise a minority of extremity cases. An adult patient with rhabdomyosarcoma in the hand, which is very rare, is presented in this article. General characteristics of the tumour and the treatment strategies are discussed.en_US
dc.identifier.doi10.3109/2000656X.2012.731580en_US
dc.identifier.endpage424en_US
dc.identifier.issn2000-656Xen_US
dc.identifier.issue5en_US
dc.identifier.pmid23356943en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage422en_US
dc.identifier.urihttps://dx.doi.org/10.3109/2000656X.2012.731580
dc.identifier.urihttps://hdl.handle.net/20.500.12395/29791
dc.identifier.volume47en_US
dc.identifier.wosWOS:000324533400017en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherINFORMA HEALTHCAREen_US
dc.relation.ispartofJOURNAL OF PLASTIC SURGERY AND HAND SURGERYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectRhabdomyosarcomaen_US
dc.subjectadulten_US
dc.subjecthanden_US
dc.titleRhabdomyosarcoma in an adult handen_US
dc.typeArticleen_US

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