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Title: [Leucocytoclastic eosinophilic vasculitis with Löffler syndrome]. Author: Sator PG, Feldmann R, Wanke T, Gschnait F, Breier F. Journal: Hautarzt; 2007 May; 58(5):440, 442-4. PubMed ID: 17066281. Abstract: Histologically, leukocytoclastic vasculitis (LV) presents with neutrophilic granulocytes with leukocytoclasia and erythrocyte extravasation, associated with variable counts of lymphocytes, plasma cells and eosinophilic granulocytes. The association of a LV with eosinophilic granulocytes and eosinophilic pneumonia was first described by Chan et al. in 1982. Our case represents the second report in the literature of this rare disease: a 85 year old patient with LV and numerous eosinophilic granulocytes in association with intermittent blood eosinophilia and Löffler syndrome (eosinophilic pulmonary infiltrates). The recurrent episodes were treated successfully with oral corticosteroids.[Abstract] [Full Text] [Related] [New Search]