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Hemophagocytic Lymphohistiocytosis Associated with Anaplasmosis
Tamara M Johnson1,2, Melinda S Brown1,2, Mohamed Rabbat1,3
1Department of Medicine, New York Medical College, School of Medicine, Valhalla, NY, USA.
Abstract:
Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome characterized by unregulated macrophage and T-lymphocyte activation resulting in cytokine overproduction and subsequent histiocytic phagocytosis. Variant infections, particularly viruses have been postulated as the inciting factor for this potentially fatal disease. Herein, we will report a case of HLH associated with anaplasmosis.
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