结果大鼠实验性肺纤维化模型成功；
Results: The rat model of pulmonary fibrosis was established.
在减轻放射性肺纤维化等晚反应方面两组相似。
It was similar to the two groups in late reaction to radioactive pulmonary fibrosis.
主要病变为弥漫性肺纤维化，有纤维细胞结节形成。
The main histopathological changes were diffuse pulmonary fibrosis and deposition of large amount of dust.
以尘斑伴灶周肺气肿为主，可有轻度弥漫性肺纤维化。
By dust spot with focal weeks emphysema is given priority to, with mild diffuse pulmonary fibrosis.
病理组织学检查亦表明，姜黄素明显改善实验性肺纤维化。
Results: Curcumin significantly reduced the elevate levels of Hyp, MDA in pulmonary tissue.
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.
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).
肺结构变形、蜂窝状囊性变、牵引性支扩和肺纤维化。
Lung distortion, honeycomb cysts, traction bronchiectasis and pulmonary fibrosis.
这句话本意是讲肺功能测定这样一个限制性通气模式的变化是因为肺纤维化改变。
The changes corresponding to fibrosis would attribute to the spirometry results a rather restrictive pattern of changes.
肺纤维化是指多种原因导致的，以弥漫性肺间质组织增生为特征的疾病。
Pulmonary fibrosis is caused by many factors and shows diffuse interstitial tissue hyperplasia.
肺纤维化是一种由多种因素引起的间质性肺疾病。
AimPulmonary fibrosis is a pulmonary interstitial disease, which is induced by many factors.
肺纤维化是一种由多种因素引起的间质性肺疾病。
AimPulmonary fibrosis is a pulmonary interstitial disease, which is induced by many factors.
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