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Rheumatology

Immune complex vasculitis and polyarteritis nodosa

The Chapel Hill 2012 map of vasculitis by vessel size. Immune complex small-vessel vasculitis (IgA vasculitis, cryoglobulinaemic, hypocomplementaemic urticarial, anti-GBM) and polyarteritis nodosa, with its microaneurysms, mononeuritis, hepatitis B link, DADA2 and treatment by Five-Factor Score.

Tier 2Condition

Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made

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At a glance

  • Chapel Hill 2012 names vasculitis by the largest vessel usually involved. This note covers medium-vessel PAN and the immune complex small-vessel group. ANCA vasculitis is in its own note; GCA in PMR and GCA.
  • Immune complex vasculitis deposits immunoglobulin and complement in vessel walls. Biopsy immunofluorescence shows it. Complement is often low (except IgA vasculitis).
  • PAN is necrotising arteritis of medium arteries, ANCA negative, with no glomerulonephritis. Think of it with mononeuritis multiplex, livedo, testicular pain and gut ischaemia.

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Sources

Last updated
14 November 2026
What changed
  • 14 November 2026 Personal emails, About story and Australian-style copy

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