Vasculitis as a complication of lymphoproliferative diseases is relati
vely uncommon. Cutaneous vasculitis is most commonly necrotizing and l
eukocytoclastic. Granulomatous vasculitis occurs rarely with lymphopro
liferative diseases, and even less commonly T-cell lymphocytic vasculi
tis with eosinophilia, The most common systemic vasculitis is caused b
y cryoglobulinemia, due to either lymphocytic lymphoma or Waldenstrom'
s macroglobulinemia, Other unusual associations involving systemic vas
culitides include polyarteritis nodosa and hairy cell leukemia, Wegene
r's granulomatosis and Hodgkin's disease, granulomatous angiitis of th
e central nervous system and lymphoma, temporal arteritis and lymphoma
, and Henoch-Schonlein purpura and lymphoma. The vasculitis may predat
e the diagnosis of the lymphoproliferative disease, and patients with
vasculitis should be screened and monitored for lymphoproliferative di
seases. Copyright (C) 1996 hy W.B. Saunders Company