特发性肺纤维化；肺痿；中医临床研究。
Idiopathic Pulmonary Fibrosis; Lung paralysis; TCM clinical study.
最可能的诊断是特发性肺纤维化（IPF）。
The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF).
特发性肺纤维化预后怎么样？具体的我们来看下。
Idiopathic pulmonary fibrosis prognosis? Specific we look at.
特发性肺纤维化以进行性肺损伤、炎症、肺组织纤维化为特征。
IPF is characterized by progressive injury, inflammation, and fibrosis of the lung parenchyma.
现结合有关文献对特发性肺纤维化的诊断和相关研究作一综述。
The literature about diagnosis and correlative study on IPF is reviewed.
最常见的药物性肺损伤表现是肺纤维化，这不足以与特发性肺纤维化鉴别。
The most common pattern seen on HRCT in patients with drug induced lung injury is that of fibrosis, indistinguishable from the appearance of idiopathic pulmonary fibrosis.
特发性肺纤维化的常见症状是咳嗽、咳痰，来说说特发性肺纤维化的病因。
Idiopathic pulmonary fibrosis of common symptom is a cough, sputum, say the cause of idiopathic pulmonary fibrosis.
方法：应用自制的生存质量测评表对36例特发性肺纤维化患者中医药干预前后的生存质量进行分析比较。
Methods: Applying the self-made life quality evaluating list, life qualities of 36 cases of IPF patients were analyzed and compared before and after the intervention of traditional Chinese medicine.
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.
方法采用酶联免疫吸附法对40例特发性肺纤维化患者和30例健康人血清基质金属蛋白酶- 9进行测定。
Methods The serum level of MMP-9 in 40 patients with IPF and 30 healthy subjects was measured by ELISA.
目的提高对CA19 9显著升高的特发性肺纤维化（IPF）的认识，评价CA19 9的升高与IPF进展的相关性。
Objective To highlight the characteristics of Idiopathic pulmonary fibrosis(IPF) with marked elevated serum carbohydrate antigen sialyl Lewis(a)(CA19-9).
目的提高对CA19 9显著升高的特发性肺纤维化（IPF）的认识，评价CA19 9的升高与IPF进展的相关性。
Objective To highlight the characteristics of Idiopathic pulmonary fibrosis(IPF) with marked elevated serum carbohydrate antigen sialyl Lewis(a)(CA19-9).
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