15 results
diagnosis lupus signs syndrome arteritis druginduced giantcell pmr polymyalgia rheumatica sle temporal treatment activation algorithm behcet classification comparison dequervains dermatology
Clinical Disease Characteristics and Suggested Algorithm for Diagnostic Evaluation of Patients With Symptoms of Polymyalgia Rheumatica #Diagnosis
Clinical Disease ... Patients With Symptoms ... #Diagnosis #Rheumatology ... #Algorithm #GCA ... GiantCell #Temporal #Arteritis
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... Behcet syndrome (Clinical ... Syndrome #diagnosis #management ... #signs #symptoms ... #rheumatology #
Eichhoff's Test in de Quervain's Tenosynovitis 1) Patient makes a fist with fingers wrapped around the thumb 2)
ulnar deviates ... reproduction of patient's symptoms ... Tenosynovitis #clinical ... #orthopedics #rheumatology ... #wrist
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 Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
arteritis (GCA) ... Diagnosis = clinical ... the “Chewing gum test ... them, but urgent rheumatology ... #Diagnosis #Management
Rheumatoid arthritis (RA): Pathogenesis and Joint diseases features • RA affects 1% of population, women >
Rheumatoid arthritis ... Joint diseases ... boggy" joints, esp carpal ... Boutonniere's ulnar ... pathophysiology #signs #symptoms
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
often causes arthritis ... branches • GCA ... Presentation - Systemic Symptoms ... retinopathy Lab Tests ... differential #diagnosis #rheumatology
Polymyalgia Rheumatica (PMR) Diagnosis and Management Summary WHAT? • Polymyalgia rheumatica (PMR) is a common systemic inflammatory
Management Summary ... CLINICAL: • Physical ... for giant cell arteritis ... diagnosed based on clinical ... #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 ... Liver function tests ... Syndrome #Diagnosis #Management ... #Hematology #Rheumatology
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
) Suspect: Clinical ... Non-autoimmune rheumatologic ... lymphoproliferative syndrome Clinical ... pain • Swan neck/Ulnar ... Induced Lupus: • Symptoms
IgG4-Related Disease Clinical history: Man, 60 years, multiorgan involvement, unique or multiple inflammatory pseudotumor 4 phenotypes: •
IgG4-Related Disease ... Clinical history ... specific laboratory tests ... #diagnosis #management ... workup #treatment #rheumatology
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