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pubmed-article:21079332pubmed:dateCreated2010-11-16lld:pubmed
pubmed-article:21079332pubmed:abstractTextCD4+/CD56+ hematodermic neoplasm, formerly known as blastic NK cell lymphoma, is a rare and aggressive neoplasm with a high incidence of cutaneous involvement, risk of leukemic dissemination and poor prognosis. The characteristic features are expression of the T helper inducer cell marker CD4 and the NK-cell marker CD56 in the absence of other T cell or NKcell specific markers. Because of the rarity of this disease, we describe a 48 year old woman suffering from CD4+/CD56+ hematodermic neoplasm on her cheek without leukemic infiltration.lld:pubmed
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pubmed-article:21079332pubmed:authorpubmed-author:KavalaMukadde...lld:pubmed
pubmed-article:21079332pubmed:authorpubmed-author:ZindanciIlkin...lld:pubmed
pubmed-article:21079332pubmed:authorpubmed-author:KocaturkEmekElld:pubmed
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pubmed-article:21079332pubmed:articleTitleCutaneous CD4+/CD56+ hematodermic neoplasm.lld:pubmed
pubmed-article:21079332pubmed:affiliationDepartment of Dermatology, Goztepe Training and Resach Hospital, Istanbul, Turkey. ilkin.dr@gmail.comlld:pubmed
pubmed-article:21079332pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21079332pubmed:publicationTypeCase Reportslld:pubmed