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特发性肺间质纤维化的治疗进展 被引量:8

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摘要 特发性肺纤维化(diopathicpulmonaryfibrosis,IPF)是一种原因不明的间质性肺疾病,其特征性病理改变为普通型间质性肺炎(usual interstial pneumonia,UIP),临床表现为进行性加重的呼吸困难伴刺激性咳嗽。诊断后的中位生存时间为3年,目前尚无有效的治疗方法。本文重点介绍该病的药物治疗进展。
出处 《江西医药》 CAS 2011年第2期191-193,共3页 Jiangxi Medical Journal
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参考文献15

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