31 results
disease lupus treatment sle arteritis erythematosus syndrome gca signs symptoms temporal stills adultonset algorithm aosd classification druginduced hematology neurology rheumatoid
Giant Cell (Temporal) Arteritis Dr. Ann Marie Kumfer @AnnKumfer #GiantCell #Temporal #Arteritis #Diagnosis #Management #GCA #rheumatology
Cell (Temporal) Arteritis ... @AnnKumfer #GiantCell ... #Temporal #Arteritis ... #Diagnosis #Management ... #GCA #rheumatology
Clinical Disease Characteristics and Suggested Algorithm for Diagnostic Evaluation of Patients With Symptoms of Polymyalgia Rheumatica #Diagnosis
Clinical Disease ... Algorithm for Diagnostic ... #Rheumatology # ... Polymyalgia #Rheumatica #GiantCell ... #Temporal #Arteritis
Temporal (Giant cell) Arteritis Risk Factors: • Age (almost never occurs before age 50) Clinical: •
Temporal (Giant cell) Arteritis ... before age 50) Clinical ... #Temporal #GiantCell ... #Arteritis #Diagnosis ... #Rheumatology #
Giant Cell Arteritis (GCA) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Visual Symptoms/Loss or
Giant Cell Arteritis ... ) - Vasculitis Management ... @MithuRheum #GiantCell ... #Arteritis #GCA ... Guidelines #algorithm #rheumatology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... w/differential diagnosis ... them, but urgent rheumatology ... #GiantCell #arteritis ... #Management
Clinical Features of Systemic Lupus (SLE) General: Fever (50%), Depression, Fatigue (75%), Weight loss (50%) Eye: Sjögrens (15%) Skin
Clinical Features ... of Systemic Lupus ... of hip (rare), Arthritis ... signs #symptoms #diagnosis ... #rheumatology
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... Fever, Arthralgia/arthritis ... solid cancers • Systemic ... #management #treatment ... #rheumatology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
fever syndromes Clinical ... Fever is the main clinical ... Activation #Syndrome #Diagnosis ... #Management #Hematology ... #Rheumatology
Antinuclear Antibodies (ANA) ANA or Anti-NucIear Antibody refers to antibodies against antigens in the nucleus → like
likely it will be clinically ... Juvenile Idiopathic Arthritis ... Juvenile Idiopathic Arthritis ... ANA #patterns #rheumatology ... #diagnosis #differential
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
maculopapular rash, arthritis ... episode (30%) Systemic ... low ferritin, arthritis ... Disease #AOSD #rheumatology ... #diagnosis #management
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