Cordier J F, Faure M, Hermier C, Brune J
Dept. of Pneumology, Hôpital Louis Pradel, Université Claude Bernard, Lyon, France.
Eur Respir J. 1990 Jan;3(1):115-8.
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.
我们报告了一名患有特发性嗜酸性粒细胞增多综合征的患者，其表现为双侧嗜酸性胸腔积液。他还患有持久性隆起性红斑，这是一种罕见的血管炎型皮肤病。未出现心肌病。经长期皮质类固醇治疗后，胸腔积液、皮肤病变和血液嗜酸性粒细胞增多均消失。
