Recent research progress and therapeutic condition of Idiopathic Pulmonary Interstitial Fibrosis(IPIF) were reviewed.
就近来对特发性肺间质纤维化的研究进展及治疗现状进行分析。
Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.
与矽肺的发病相似，特发性肺纤维化(IPF)也是以肺成纤维细胞大量增殖为主要特征的肺纤维化疾病。
Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.
与矽肺的发病相似，特发性肺纤维化(IPF)也是以肺成纤维细胞大量增殖为主要特征的肺纤维化疾病。
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