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pubmed-article:19554151pubmed:dateCreated2009-6-25lld:pubmed
pubmed-article:19554151pubmed:abstractTextExtraskeletal Ewing's sarcoma (EES) is a rare, soft tissue, malignant neoplasm histologically similar to skeletal Ewing's sarcoma. It occurs mainly in adolescents and young adults, and affects extremities in 36% of cases and central locations (commonly paravertebral regions) in the remainder. The differential diagnosis includes other small, blue, round cell tumours. A clinical case of EES involving a great toe in a young boy is reported. EES diagnosis was confirmed by features of histological analysis and immunohistochemistry, and by the presence of the t(11;22) chromosomal translocation.lld:pubmed
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pubmed-article:19554151pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:19554151pubmed:issn1195-2199lld:pubmed
pubmed-article:19554151pubmed:authorpubmed-author:MeilikBenjami...lld:pubmed
pubmed-article:19554151pubmed:authorpubmed-author:ZukerRonald...lld:pubmed
pubmed-article:19554151pubmed:authorpubmed-author:CypelTatiana...lld:pubmed
pubmed-article:19554151pubmed:issnTypePrintlld:pubmed
pubmed-article:19554151pubmed:volume15lld:pubmed
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pubmed-article:19554151pubmed:pagination165-8lld:pubmed
pubmed-article:19554151pubmed:year2007lld:pubmed
pubmed-article:19554151pubmed:articleTitleExtraskeletal Ewing's sarcoma in a great toe of a young boy.lld:pubmed
pubmed-article:19554151pubmed:affiliationThe Hospital for Sick Children, Toronto, Ontario.lld:pubmed
pubmed-article:19554151pubmed:publicationTypeJournal Articlelld:pubmed