RHeumatology
study of connective tissue diseases
Immunology Dx
Chronic pain syndromes
Complex regional pain syndrome
Fibromyalgia
Growing pains
Myopathies
Metabolic myopathies
Idiopathic inflammatory myopathies
Juvenile arthritis
Juvenile idiopathic arthritis
Polyarticular juvenile idiopathic arthritis
Psoriatic juvenile idiopathic arthritis:
Spondyloarthritis (seronegative ie rheumatoid-factor negative) but associated with human-leukocyte antigen (HLA)-B27
Vasculitis
Large-vessel vasculitis
Periodic fever syndromes
Systemic lupus erythematosus
Scleroderma
Raynaud phenomenon (Cold fingers)
Sjögren's syndrome (dry eyes and mouth)
Sarcoidosis
Acute Rheumatic Fever
Immunology Dx
Chronic pain syndromes
Complex regional pain syndrome
Fibromyalgia
Growing pains
Myopathies
Metabolic myopathies
Idiopathic inflammatory myopathies
- Juvenile dermatomyositis
- Polymyositis
Juvenile arthritis
Juvenile idiopathic arthritis
- Systemic JIA
- Polyarticular JIA
- Oligoarticular JIA
Polyarticular juvenile idiopathic arthritis
Psoriatic juvenile idiopathic arthritis:
Spondyloarthritis (seronegative ie rheumatoid-factor negative) but associated with human-leukocyte antigen (HLA)-B27
- Enthesitis-related arthritis (ERA)
- Juvenile ankylosing spondylitis (JAS)
- Psoriatic JIA
- Reactive arthritis
- Inflammatory bowel disease (IBD)-associated arthritis
Vasculitis
Large-vessel vasculitis
- Giant cell (temporal) arteritis (not seen in children)
- Takayasu arteritis
- Polyarteritis nodosa
- Kawasaki disease
- Primary angiitis of the central nervous system
- Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitides (AAV)
- granulomatosis with polyangiitis (GPA, previously Wegener's Granulomatosis) (c-ANCA) + associated with antiproteinase 3 Ab
- Microscopic polyangiitis (MPA) including renal-limited vasculitis (RLV) (p-ANCA) + associated with antimyeloperoxidase Ab
- Eosinophilic granulomatosis with polyangiitis (EGPA, previously Churg-Strauss)
- (All have similar features on renal histology: a focal necrotizing, often crescentic, pauci-immune glomerulonephritis)
- Immune complex small-vessel vasculitis
- Antiglomerular basement membrane disease (Goodpasture's syndrome)
- Cryoglobulinemic vasculitis
- Henoch-Schönlein purpura (IgA vasculitis)
- Hypocomplementemic urticarial vasculitis
- Behçet's syndrome
- Cogan's syndrome
- Single-organ vasculitis
- Secondary Vasculitis
- Vasculitis associated with probable etiology
- Monogenic Vasculitis
Periodic fever syndromes
Systemic lupus erythematosus
Scleroderma
Raynaud phenomenon (Cold fingers)
Sjögren's syndrome (dry eyes and mouth)
Sarcoidosis
Acute Rheumatic Fever