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diagnosis lymphohistiocytosis management hematology hemeonc rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Hemophagocytic Lymphohistiocytosis ... →Activation of CD8 ... Purtilo (XLP) Acquired ... #Hemophagocytic ... #summary #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
Hemophagocytic Lymphohistiocytosis ... HLH is a critical ... • Secondary (Acquired ... Clinical Presentation ... #HLH #Hemophagocytic
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