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diagnosis hemophagocytic hlh lymphohistiocytosis management rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
→Activation of CD8 ... IFN-y) → Excessive activation ... adenopathies, confusion ... B-LNH), solid cancers ... #summary #rheumatology
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