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Assessment of the Metabolic Profile of Primary Leukemia Cells
Published on: November 21, 2018
Hemophagocytic Lymphohistiocytosis Associated with Natural T-cell Leukemia
Frank R Ricaurte1, Tariq Kewan2, Pravallika Chadalavada3
1Hematology and Oncology, Cleveland Clinic - Fairview Hospital, Cleveland, USA.
Abstract:
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening syndrome of excessive immune activation. It can be triggered by a variety of events that disrupt immune homeostasis, infection being the most common of them. We report a case of a 36-year-old male diagnosed with HLH associated with natural T-cell leukemia. The purpose of this report is to call attention to the clinical presentation, diagnosis, and treatment of HLH.
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