| Literature DB >> 2178960 |
J F Cordier1, M Faure, C Hermier, J Brune.
Abstract
We report a patient with idiopathic hypereosinophilic syndrome presenting with bilateral eosinophilic pleural effusions. He also had erythema elevatum diutinum, a rare skin disease of the vasculitic type. No cardiomyopathy was present. Pleural effusions, skin lesions, and blood eosinophilia disappeared with prolonged corticosteroid treatment.Entities:
Mesh:
Year: 1990 PMID: 2178960
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671