ANCA-associated vasculitides

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ANCA-associated vasculitides (AAV) are diseases caused by vasculitis in which antineutrophil cytoplasmic antibodies (ANCAs) can be detected in the blood.^[1]^[2]

Types

Three AAVs are Churg-Strauss syndrome, microscopic polyangiitis and Wegener's granulomatosis. All feature a small-vessel vasculitis.

Polyarteritis also presents with ANCA.^[3]

References

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Systemic CT disorders (M32-M36, 710)

General

Systemic lupus erythematosus: Drug-induced SLE · Libman-Sacks endocarditis

Inflammatory myopathy/Myositis: Dermatopolymyositis (Dermatomyositis/Juvenile dermatomyositis, Polymyositis) · Inclusion body myositis

Scleroderma: Systemic scleroderma (Progressive systemic sclerosis, CREST syndrome)

Overlap syndrome / Mixed connective tissue disease

Other hypersensitivity/autoimmune

Sjögren's syndrome

Other

Behçet's disease · Polymyalgia rheumatica · Eosinophilic fasciitis · Eosinophilia–myalgia syndrome · fibrillin (Marfan syndrome, Congenital contractural arachnodactyly)

M: MUS, DF+DRCT

anat (h/n, u, t/d, a/p, l)/phys/hist

noco(m, s, c)/cong(d)/tumr, sysi/epon, injr

proc, drug (M1A/3)

pt:Vasculites associadas ao ANCA

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