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1 Introduction Hemophagocytic syndrome, also known as hemophagocytic lymphohistiocytosis (HLH), is a life-threatening inflammatory condition driven by an overactive immune response that can severely impair organ function (1). Clinically, HLH is characterized by persistent fever, elevated ferritin levels, splenomegaly, cytopenias, and coagulopathy (2, 3). Liver involvement is especially prevalent, typically manifesting as liver injury.
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