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dc.contributor.authorKavala, Mukaddes
dc.contributor.authorKoc, Melek
dc.contributor.authorBÜYÜKBABANİ, Nesimi
dc.contributor.authorKocaturk, Emek
dc.contributor.authorZindanci, Ilkin
dc.date.accessioned2022-02-18T09:22:41Z
dc.date.available2022-02-18T09:22:41Z
dc.date.issued2010
dc.identifier.citationZindanci I., Kavala M., BÜYÜKBABANİ N., Kocaturk E., Koc M., "Cutaneous CD4+/CD56 hematodermic neoplasm", INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, cilt.76, sa.6, 2010
dc.identifier.issn0378-6323
dc.identifier.otherav_356d626b-5788-4d86-bf59-f680000e9a5a
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177091
dc.identifier.urihttps://doi.org/10.4103/0378-6323.72471
dc.description.abstractCD4+/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.
dc.language.isoeng
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatology
dc.subjectDermatoloji
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.titleCutaneous CD4+/CD56 hematodermic neoplasm
dc.typeMakale
dc.relation.journalINDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY
dc.contributor.departmentGoztepe Training & Resach Hosp , ,
dc.identifier.volume76
dc.identifier.issue6
dc.contributor.firstauthorID3378238


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