Description

Criteria for the diagnosis of cutaneous leukocytoclastic angiitis were proposed at an International Consensus Conference held at the University of North Carolina, Chapel Hill, North Carolina.


 

NOTE: The term "hypersensitivity vasculitis" was not used at the conference. This was felt to represent either microscopic polyangiits or cutaneous leukocytoclastic angiitis rather than a separate entity (page 191).

 

Lesion: vasculitis affecting small blood vessels

Vessel

Involvement

venules

yes

capillaries

yes

arterioles

yes

small arteries

no

medium-sized arteries

no

large arteries

no

 

The only manifestation should be skin involvement.

 

The presence of glomerulonephritis or systemic involvement suggests another form of vasculitis. Occasionally a systemic vasculitis will first present with cutaneous involvement, with vasculitis in other organs appearing later.

 

Differential diagnosis:

(1) Henoch Schonlein purpura - IgA immune deposits

(2) microscopic polyangiitis - no or rare immune deposits, ANCA positive

(3) serum sickness - immune complex deposits

(4) SLE - high serum titers to ANA

(5) Wegener's granulomatosis - granulomatous inflammation, ANCA positive

(6) Churg-Strauss syndrome -eosinophilia and asthma, ANCA positive

(7) essential cryoglobulinemia - cryoglobulin deposits

 


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