37 results
diagnosis rheumatology disease vasculitis differential giantcell lupus rheumatoid algorithm aosd autoimmune dermatology druginduced gca hemophagocytic hlh lymphohistiocytosis myositis neurology oncology
Giant Cell (Temporal) Arteritis: Pathogenesis and investigations Risk Factors: - Unclear environmental triggers (may be viral, not
Cell (Temporal) Arteritis ... environmental triggers ... yrs old; F>M Signs ... GiantCell #Temporal #Arteritis ... #Pathophysiology
Rheumatoid Arthritis Summary MCP and PIP Involvement, Spares DIP, Carpal Tunnel, Sicca Syndrome, Epi/Scleritis, Heart Disease, Rheumatoid
Rheumatoid Arthritis ... Tunnel, Sicca Syndrome ... #Rheumatoid #Arthritis ... RA #diagnosis #rheumatology ... #signs #symptoms
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
myocarditis, coronary arteritis ... SLE, Reactive arthritis ... Ocular melanoma • Arthritis ... SLE, Reactive Arthritis ... #signs #symptoms
Leukostasis vs Tumor Lysis Syndrome Leukostasis: • Pathophysiology: Large, immature blasts and high WBC count cause hyperviscosity
Leukostasis: • Pathophysiology ... • Triggers: Diuretics ... WBC >100k, + lab signs ... TLS #diagnosis #management ... #hematology
Primary Sjogren’s Syndrome: Pathogenesis and Clinical Findings • Primary Sjögren's is a solitary process whereas secondary Sjögren's
like rheumatoid arthritis ... / Symptoms: - ... #Pathophysiology ... #Diagnosis #Signs ... #Symptoms
Giant Cell Arteritis (GCA) - Vasculitis Management Algorithm - ACR/VF 2021 Guidelines • Visual Symptoms/Loss or
Giant Cell Arteritis ... ) - Vasculitis Management ... Without Visual Symptoms ... MithuRheum #GiantCell #Arteritis ... #Treatment #ACR2021
Autoimmune Myositis Necrotizing myopathy is associated with higher CK levels, greater level of muscle weakness, less systemic
less systemic symptoms ... , holster sign, ... anti-synthetase syndrome ... myositis, and arthritis ... after 2 years of treatment
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
susceptibility, infectious triggers ... maculopapular rash, arthritis ... low ferritin, arthritis ... #diagnosis #management ... #treatment
Sweet Syndrome Acute febrile neutrophilic dermatosis (Sweets Syndrome) is a skin condition characterized by fever and inflamed
of the joints (arthritis ... Episcleritis Signs ... of the joints (arthritis ... Neutrophilic rheumatoid arthritis ... Treatment: - Systemic
Approach to Headaches - Differential Diagnosis Algorithm Red flags (PHANTOMS): • Pattern change, progressively worse, papilledema •
papilledema • Horner syndrome ... artery tenderness, triggered ... ) • Systemic symptoms ... and signs (e.g. ... ) • Temporal arteritis
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