17 results
diagnosis management syndrome igg4 signs acr2021 activation adult algorithm aosd arteritis behcet behcets biliary cirrhosis classification diagnossi erythematosus gammopathy gca
Polyarteritis Nodosa (PAN) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Severe Disease → Remission
Nodosa (PAN) - Vasculitis ... • Non-Severe Disease ... immunosuppressive agent (e.g ... #Management #Treatment ... Guidelines #algorithm #rheumatology
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
Diagnosis Diagnostic Criteria ... the following 4 criteria ... Uveitis or retinal vasculitis ... retinal vasculitis ... #rheumatology
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
the most common vasculitis ... Diagnostic Criteria ... #KD #vasculitis ... #rheumatology # ... diagnossi #management #treatment
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
Summary Diagnostic Criteria ... When present, symptoms ... • "Vasomotor" symptoms ... von Willebrand disease ... #hematology
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
, small-vessel vasculitis ... meningitis), MCC CNS symptoms ... Arthritis, AS Treatment ... management #signs #symptoms ... #rheumatology #
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
the chest/trunk Symptoms ... Treatment - Mild ... : NSAIDS Treatment ... Prednisone 0.5-1mg/kg ... AOSD #diagnosis #rheumatology
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
IgG4-Related Disease ... No necrosis, No vasculitis ... Glucocorticoids (0.6 mg/kg ... IgG4 #Related #Disease ... #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
• Infection (eg ... Histopathologic criteria ... Treatment: • Corticosteroids ... Diagnosis #Management #Hematology ... #Rheumatology
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
Non-autoimmune rheumatologic ... . hematologic) ... vein thrombosis Hematologic ... Induced Lupus: • Symptoms ... Erythematosus #Diagnosis #Rheumatology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
systemic inflammatory vasculitis ... of the steroid treatment ... Treatment of GCA ... them, but urgent rheumatology ... Temporal #Signs #Symptoms
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