• Hautarzt · May 2007

    [Leucocytoclastic eosinophilic vasculitis with Löffler syndrome].

    • P-G Sator, R Feldmann, T Wanke, F Gschnait, and F Breier.
    • Dermatologische Abteilung, Krankenhaus Hietzing mit Neurologischem Zentrum Rosenhügel, 1130, Wien. paul.sator@wienkav.at
    • Hautarzt. 2007 May 1;58(5):440, 442-4.

    AbstractHistologically, 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.

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