Recognition of hemophagocytic lymphohistiocytosis in sickle cell vasoocclusive crises is a potentially lifesaving diagnosis.

Orly Leiva,Lillian McMahon,J Mark Sloan,John Lee,Adam Lerner

HAEMATOLOGICA（2019）

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摘要

Hemophagocytic lymphohistiocytosis (HLH) is a rare but aggressive and potentially life-threatening syndrome caused by a hyperinflammatory response leading to organ damage.[1][1],[2][2] It is characterized by fevers, cytopenias, hepatosplenomegaly, hyperferritinemia, hypertriglyceridemia and

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Laboratory Hematology,Red Cells,hemophagocytic lymphohistiocytosis,sickle cell disease

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