Hemophagocytic syndrome with erythrocyte phagocytosis by the myeloid precursors in a patient with AML-M2

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dc.contributor.authorYilmaz M.
dc.contributor.authorVural F.
dc.contributor.authorTöbü M.
dc.contributor.authorErtan Y.
dc.contributor.authorBüyük F.
dc.date.accessioned2019-10-26T23:57:19Z
dc.date.available2019-10-26T23:57:19Z
dc.date.issued2008
dc.departmentEge Üniversitesien_US
dc.description.abstractHemophagocytic syndrome is characterized by fever, fatigue, weight loss, lymphadenopathy, and laboratory abnormalities including pancytopenia, liver dysfunction, hypertriglyceridemia and hyperfibrinemia. Histopathologically, lesions are characterized by mononuclear cell infiltration with marked histiocyte proliferation and phagocytosis of erythrocytes, leukocytes, platelets and their precursors by activated macrophages in the reticuloendothelial tissues. Hemophagocytic syndrome may develop from strong immunological stimuli such as severe infection, malignancy and autoimmune diseases. We present a 73-year-old man with acute myeloblastic leukemia FAB M2 type (AML M2) whose bone marrow histology showed unusual hemophagocytosis by myeloid cells and myeloblasts. © Turkish Society of Hematology.en_US
dc.identifier.endpage44en_US
dc.identifier.issn1300-7777
dc.identifier.issue1en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage42en_US
dc.identifier.urihttps://hdl.handle.net/11454/20991
dc.identifier.volume25en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Hematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcute myeloblastic leukemiaen_US
dc.subjectAMLen_US
dc.subjectHemophagocytic syndromeen_US
dc.titleHemophagocytic syndrome with erythrocyte phagocytosis by the myeloid precursors in a patient with AML-M2en_US
dc.typeArticleen_US

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