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Autor:
Tasaduq Fazili, Dorothy C Garner, Ekta Bansal, Vijayendra Bajwa, Charles Schleupner, Harpreet Kaur
Publikováno v:
American Journal of Medical Case Reports. 9:557-563
Introduction: Hemophagocytic lymphohistiocytosis (HLH) is an uncommon condition characterized by abnormal, excessive immune activation resulting in severe cytopenias from an uncontrolled inflammatory response. It can be primary/ familial or secondary