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signs management vasculitis differential disease syndrome arteritis behcet classification criteria gca giantcell pan pathophysiology polyarteritisnodosa polychondritis primary relapsing scleroderma sclerosis
Behcet's Syndrome - Diagnosis Diagnostic Criteria for Behget's Syndrome (International Study Group for Behget's Disease): • Recurrent,
- Diagnosis Diagnostic ... idiopathic oral ulcers ... Recurrent genital ulcers ... test Most Common Clinical ... #criteria #rheumatology
Primary Syphilis Usually, a single ulcer (chancre) appears at the site where the bacteria entered the body.
Usually, a single ulcer ... nodes near the ulcer ... weeks ▪ Multiple lesions ... #Diagnosis #Clinical ... #Photo
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... meningitis), MCC CNS symptoms ... syndrome (Clinical ... management #signs #symptoms ... #rheumatology #
Systemic Sclerosis (Scleroderma) Multi-system autoimmune disease characterized by vasculopathy and progressive fibrosis of skin and internal organs 3
and pepper" skin changes ... Raynaud's, digital ulcers ... Scleroderma #SSc #rheumatology ... #diagnosis #signs ... #symptoms #testing
Polyarteritis Nodosa (PAN): Pathogenesis and Clinical Findings Medical Comorbidities Malignancies (most commonly hairy-cell leukemia) Immunogenetic Predisposition: patient is
Pathogenesis and Clinical ... Hypertension - Renal Insufficiency ... Peripheral sensory changes ... Pathophysiology #Diagnosis ... #Signs #Symptoms
Vasculitis - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions • Mononeuritis multiplex • Hematuria, proteinuria,
Presentation: Systemic Symptoms ... • Progressive symptoms ... and gray matter changes ... vasculitis • Behcet ... #Rheumatology
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
livedo reticularis, ulcers ... VASCULITIS: • Behçet ... genital aphthous ulcers ... Presentation - Systemic Symptoms ... #rheumatology #
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
Diagnosis = clinical ... headaches, vision changes ... them, but urgent rheumatology ... absence of visual symptoms ... Temporal #Signs #Symptoms
Relapsing Polychondritis What is it? Recurrent inflammation of the cartilage in the body (Autoimmune disorder) Who? • Most frequently: 40
ethnicities Symptoms ... + Nonspecific symptoms ... failure • Renal insufficiency ... Sarcoidosis • Behcet ... Polychondritis #rheumatology
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