Shijubo N, Fujishima T, Morita S, Nakata H, Satoh M, Uno E, Morikawa T, Abe S
Third Dept of Internal Medicine, Sapporo Medical University School of Medicine, Japan.
Eur Respir J. 1995 Feb;8(2):327-30. doi: 10.1183/09031936.95.08020327.
A 34 year old Japanese woman was referred to our university hospital due to pulmonary opacities and bilateral hilar lymphadenopathy on chest X-ray. She also had uveitis, erythematous skin nodules, and oral and genital ulcers. Laboratory data showed eosinophilia in the circulation and bronchoalveolar lavage fluid. Histological study revealed massive eosinophilic infiltration and noncaseating epithelioid granulomas in the lung and mediastinal lymph node, without evidence of vasculitis. Pulmonary opacities, lymphadenopathy, and blood eosinophilia promptly improved with corticosteroid therapy. In this patient, idiopathic chronic eosinophilic pneumonia overlapped with features of sarcoidosis and Behçet's disease.
一名34岁的日本女性因胸部X线显示肺部有阴影和双侧肺门淋巴结肿大而被转诊至我校医院。她还患有葡萄膜炎、皮肤红斑结节以及口腔和生殖器溃疡。实验室检查数据显示循环血液和支气管肺泡灌洗液中存在嗜酸性粒细胞增多。组织学研究显示肺部和纵隔淋巴结有大量嗜酸性粒细胞浸润和非干酪样上皮样肉芽肿,无血管炎证据。使用皮质类固醇治疗后,肺部阴影、淋巴结肿大和血液嗜酸性粒细胞增多迅速改善。该患者患有特发性慢性嗜酸性粒细胞性肺炎,同时具有结节病和白塞病的特征。