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dc.contributor.authorEsmaili, HA
dc.contributor.authorNiknejad, MT
dc.contributor.authorMohajeri, S
dc.date.accessioned2018-08-26T07:44:11Z
dc.date.available2018-08-26T07:44:11Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/48144
dc.description.abstractEwing's sarcoma is one of the most common primary bone tumors of childhood. The tumor is almost always metaphyseal or diaphyseal, within long, bones. In children; lesions of the epiphysis are often benign, with the most common diagnosis being chondroblastoma. Rarely, 1%-2% of Ewing sarcomas may involve epiphysis. We present a case of Ewing's sarcoma of the proximal humeral epiphysis in a 13-year-old boy: This case adds to previously reported cases of epiphyseal Ewing sarcoma and suggests that the diagnosis should be considered: for pediatric epiphyseal lesions.
dc.language.isoEnglish
dc.relation.ispartofARCHIVES OF IRANIAN MEDICINE
dc.subjectEpiphysis
dc.subjectEwing's sarcoma
dc.subjectprimary malignant bone tumor
dc.titleEwing's Sarcoma of Proximal Humeral Epiphysis
dc.typeArticle
dc.citation.volume18
dc.citation.issue2
dc.citation.spage133
dc.citation.epage134
dc.citation.indexWeb of science


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