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特发性肺纤维化与肺动脉高压 被引量：1

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摘要 特发性肺纤维化（idiopathic pulmonary fibrosis,IPF）是指原因不明并以普通型间质性肺炎（usual interstitial pneumonia,UIP）为特征性病理改变的一种慢性炎症性间质性疾病，主要表现为弥漫性肺泡炎、肺泡单位结构紊乱和肺纤维化。病情多呈进行性发展，晚期可出现发绀、肺动脉高压（pulmonary arterial hypertension, PAH）、肺源性心脏病、右心功能不全等。
作者 李惠萍
机构地区 同济大学附属上海市肺科医院呼吸科
出处 《内科理论与实践》 2008年第6期382-386,共5页 Journal of Internal Medicine Concepts & Practice
关键词 特发性肺纤维化 肺动脉高压 发病机制
分类号 R563.9 [医药卫生—呼吸系统] R543.2 [医药卫生—内科学]
  • 相关文献

参考文献13

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二级参考文献47

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共引文献16

同被引文献29

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内科理论与实践
2008年 第6期

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