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Disseminated histoplasmosis associated with acquired hemophagocytic lymphohistiocytosis
Ashish Rajput1, Isabelle Bence-Bruckler2, Lothar Huebsch2
1Division of Hematopathology, The Ottawa Hospital Ottawa, Ontario, Canada ; Eastern Ontario Regional Laboratory Association Ottawa, Ontario, Canada.
Abstract:
Hemophagocytic lymphohistiocytosis (HLH) is a potentially life-threatening clinical syndrome caused by uncontrolled activation of lymphocytes and histiocytes resulting in high levels of cytokines. Acquired HLH occurs in autoimmune, inflammatory, infectious, and immunosuppressive disorders. Prompt identification and treatment of an underlying triggering cause improves clinical outcome.
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