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management diagnosis hematology syndrome hivaids infections opportunistic pharmacology prevention chronic oncology stills adultonset aosd cll hemophagocytic hlh leukemia lupus lymphocytic
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's ... Disease Clinical ... autoinflammatory diseases ... diagnosis #management #treatment ... #rheumatology
IDSA 2017 CDiff Guidelines - Table 1. Recommendations for the Treatment of Clostridium difficile Infection in Adults #Management
IDSA 2017 CDiff ... Guidelines - Table ... Recommendations for the Treatment ... difficile Infection in Adults ... IDSA2017 #Guidelines #Adults
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's ... Disease (AOSD) ... synovitis (40%) Treatment ... AdultOnset #Stills #Disease ... #AOSD #rheumatology
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
common leukemia in adults ... Affects mainly older adults ... cells can indicate disease ... microglobulin Treatment ... workup #oncology #hematology
Susac Syndrome - Clinical Triad - Central nervous system dysfunction - Branch retinal artery occlusion -
- Recurrent disease ... flares - 2-year ... arterioles - Treatment ... Diagnosis #Management #Rheumatology
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Adult Onset Still's ... Treatment - Mild ... : NSAIDS Treatment ... anti-lL6R, anti-ILI #Adult ... AOSD #diagnosis #rheumatology
Chronic Lymphocytic Leukemia (CLL) - Summary Overview: • Most common leukemia in adults • Disorder of
common leukemia in adults ... transformation) Treatment ... chemotherapy for low-risk disease ... AIHA, PRCA) • Treatment ... Leukemia #oncology #hematology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
• Autoimmune diseases ... : SLE+++, Adult-onset ... Still disease, ... Unknown cause Treatment ... #summary #rheumatology
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
Kawasaki Disease ... Summary Kawasaki Disease ... rarely occurs in adults ... KD #vasculitis #rheumatology ... diagnossi #management #treatment
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
Syndrome Systemic disease ... Epidemiology: • Young adults ... Arthritis, AS Treatment ... signs #symptoms #rheumatology ... #disease
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