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diagnosis management behcet classification disease hematology hemophagocytic hodgkins lymphohistiocytosis oncology signs summary symptoms syndrome treatment
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
accumulation of clinical ... • Clinical: fever ... , B-cell lymphoma ... diseases: SLE+++, Adult-onset ... treatment #summary #rheumatology
Hodgkin's Lymphoma Overview Hodgkin's lymphoma (HL) is an uncommon hematological malignancy arising from mature B cells. It
history • Young adults ... - Clinical Presentation ... Immunohistochemical studies (to differentiate ... HL from other lymphomas ... classification #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Epidemiology: • Young adults ... association • M > F Clinical ... Behcet disease) Differential ... Ischemia, Leukemia, Lymphoma ... signs #symptoms #rheumatology
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