Karen A Francolla

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Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially fatal disorder. It is characterized by excessive proinflammatory cytokine release and proliferation of activated macrophages and lymphocytes that phagocytose erythrocytes, white blood cells, and platelets in the bone marrow. Clinically, it presents with high persistent fever and(More)
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