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diagnosis management hemophagocytic lymphohistiocytosis gastroenterology hemeonc hemochromatosis hepatology rheumatology summary treatment
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
) Pathophysiology ... , Hb), Hepatic dysfunction ... Drugs, Unknown cause ... inhibitors under evaluation ... treatment #summary #rheumatology
Algorithm regarding the diagnosis and treatment of Hereditary Hemochromatosis HH. Step 1: In the patient with
Algorithm regarding ... normal, further evaluation ... C282Y homozygote, evaluation ... including liver and hematologic ... hemochromatosis #algorithm
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
cytopenias and organ dysfunction ... hyperinflammatory syndrome caused ... Persistent fever, organ dysfunction ... Pathophysiology ... Diagnosis #Management #Hematology
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