特发性肺纤维化严重程度分期的研究进展被引量：8

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摘要特发性肺纤维化（idiopathic pulmonary fibrosis,IPF）是一种特殊类型、原因不明的、发生于成人的、慢性进行性间质性肺病（interstitial lung disease,ILD）.影像学和（或）组织学符合寻常型间质性肺炎（usual interstitial pneumonia,UIP）,好发于老年人,目前尚缺乏有效的治疗药物,平均生存期仅为2.5～3.5年.

作者陈丹琦苏奕亮李惠萍

机构地区同济大学附属上海市肺科医院呼吸科浙江省宁波市鄞州区第二医院重症监护科

出处《中华结核和呼吸杂志》 CAS CSCD 北大核心 2018年第5期355-358,共4页 Chinese Journal of Tuberculosis and Respiratory Diseases

关键词特发性肺纤维化 PULMONARY PNEUMONIA 寻常型间质性肺炎分期间质性肺病平均生存期原因不明

分类号 R563 [医药卫生—呼吸系统]

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