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diagnosis hematology syndrome symptoms activation anemia autoimmune behcet dermatology gca giantcell hemeonc hemolytic hemophagocytic hlh lymphohistiocytosis macrophage mas sapho temporal
Autoimmune Hemolytic Anemia (AIHA) Treatment Warm AIHA: 1) Steroids - 1-2 mg/kg prednisone daily • Until
- 1-2 mg/kg prednisone ... esp if severe disease ... Polyclonal: - Infection ... #Treatment #management ... #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
, AS Treatment: ... monoclonal TNF-aIpha ... Syndrome #diagnosis #management ... #signs #symptoms ... #rheumatology #
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
systemic sx + signs ... vasculitis vs infection ... Treatment of GCA ... them, but urgent rheumatology ... Symptoms #Diagnosis #Management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
idiopathic arthritis ... SLE], AOSD) • Infection ... Treatment: • Corticosteroids ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
nonerosive inflammatory arthritis ... causes such as infectious ... and lower jaw Treatment ... SAPHO #Syndrome #Rheumatology ... #diagnosis #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
Triggers: ▪ Infections ... ▪ Autoimmune diseases ... Presentation • Common Signs ... underlying trigger: Infections ... #Hematology #HemeOnc
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