特发性肺纤维化
医学
肺纤维化
肺
发病机制
病因学
病理
纤维化
内科学
作者
Moisés Selman,Mayra Mejía,Annie Pardo
出处
期刊:Springer eBooks
[Springer Nature]
日期:2007-11-24
卷期号:: 41-45
被引量:495
标识
DOI:10.1007/978-1-84628-326-0_6
摘要
Idiopathic pulmonary fibrosis (IPF) (or cryptogenic fibrosing alveolitis) is an archetypal example of lung fibrosis. Although it is the most frequent of all, its etiology is not known, its pathogenesis only partially resolved, and its therapy quite inadequate and inefficient.KeywordsIdiopathic Pulmonary FibrosisInterstitial Lung DiseaseConnective Tissue Growth FactorUsual Interstitial PneumoniaOpen Lung BiopsyThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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