Three Cases with Langerhans Cell Histiocytosis with Sistemic Involvement [Sistemik Tutulum ile Giden Langerhans Hücreli Histiositozis'li Üç Vaka Sunumu]

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dc.contributor.authorKöksal Y.
dc.contributor.authorGülyüz A.
dc.contributor.authorÇalişkan Ü.
dc.contributor.authorReisli I.
dc.contributor.authorUçar C.
dc.date.accessioned2020-03-26T16:55:42Z
dc.date.available2020-03-26T16:55:42Z
dc.date.issued2004
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractHistiocytosis which is a proliferative process characterized by an accumulation of dentritic cells in various tissues and organs is a rare disease. It can occur as an isolated lesion or as widespread systemic disease involving virtually any body site. Langerhans cell histiocytosis was diagnosed by light microscopy in a 27-month-old boy and 16-month-old girl with anemia hepatosplenomegaly, exanthema and lesions on the skull and a 9-month-old girl with thymic and cutaneous involvement. Clinical and laboratory findings of the cases are discussed in the light of literature.en_US
dc.identifier.endpage51en_US
dc.identifier.issn1301-8825en_US
dc.identifier.issue1en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage47en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/19309
dc.identifier.volume14en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofTHOD - Turk Hematoloji-Onkoloji Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectChildhooden_US
dc.subjectLangerhans cell histiocytosisen_US
dc.subjectLiveren_US
dc.subjectLungen_US
dc.subjectThymusen_US
dc.titleThree Cases with Langerhans Cell Histiocytosis with Sistemic Involvement [Sistemik Tutulum ile Giden Langerhans Hücreli Histiositozis'li Üç Vaka Sunumu]en_US
dc.typeArticleen_US

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