结果大鼠实验性肺纤维化模型成功；
Results: The rat model of pulmonary fibrosis was established.
肺纤维化治疗困难，预后差。
Pulmonary fibrosis is difficult to cure and has a bad prognosis.
特发性肺纤维化；肺痿；中医临床研究。
Idiopathic Pulmonary Fibrosis; Lung paralysis; TCM clinical study.
目的研究纤维连接蛋白在肺纤维化中的作用。
Objective To study the roles of fibronectin played in rat pulmonary fibrosis.
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.
方法小鼠气管内注入BLM复制肺纤维化模型。
Method A single dose of BLM was intratracheally injected to induce pulmonary fibrosis of mice.
肺纤维化所致呼吸循环衰竭是致死的主要原因。
Pulmonary fibrosis caused by respiratory and circulatory failure is the main cause of death.
仅有大约1%的这种病人出现明显的肺纤维化。
Only about 1% of such persons get a significant degree of 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.
目的：探讨矽肺纤维化同生物活性介质之间的关系。
Objective: To study the relation of pulmonary fibrosis and bioactivity mediums.
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.
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.
三色染色把肺纤维化病人的结缔组织中的胶原纤维染成蓝色。
A trichrome stain highlights the collagenous connective tissue of pulmonary fibrosis in blue.
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.
结论：益阴活血汤通过抑制肺纤维化细胞因子产生肺纤维化作用。
Conclusion: the Decoction for Supplementing Yin and Activating Blood Circulation can reduce the degree of fibrosis of the lungs by checking fibrosis cell factor.
目的：观察中药肺宁对博莱霉素诱导的大鼠肺纤维化早期的防治作用。
AIM: To study the effect of Chinese medicine Feining on early experimental pulmonary fibrosis in rats induced by bleomycin.
该文就近年来关于百草枯所致肺纤维化发生机制的研究进展进行综述。
Recent studies on the pathogenesis of paraquat-induced pulmonary fibrosis are reviewed in this paper.
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.
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.
目的：观察雾化吸入布地奈德对大鼠肺纤维化的干预作用并探讨其作用机制。
Objective: to observe the effect of inhaled budesonide on pulmonary fibrosis induced by bleomycin in rats and to explore its mechanism.
该药能使导致肺纤维化的炎症得以减轻，在过去10年里被应用于硬皮病患者。
The drug decreases the inflammation that causes pulmonary fibrosis and has been used on scleroderma patients for the last 10 years.
目的研究昆布提取物j201对大鼠肺纤维化的治疗作用及其可能的作用机制。
AIM: To investigate the protective effect of Okam extract J201 on bleomycin induced pulmonary fibrosis in rats and the underlying mechanism.
高浓度中，它可导致显著的急性肺水肿，相反慢性暴露在低浓度中可以导致显著的肺纤维化。
At high concentrations, it can cause significant acute disease with pulmonary edema, whereas chronic exposures at lower concentrations can lead to significant 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.
硬皮病其他常见的影像学表现包括：肺纤维化、消化道蠕动异常（最常见于食管）。
Other common radiologic findings in scleroderma include pulmonary fibrosis and dilation and dysmotility of the gastrointestinal tract (most commonly affecting the esophagus).
接触石棉也能引起其他疾病，如石棉肺(肺纤维化)、胸膜斑、胸膜增厚和胸腔积液。
Asbestos exposure is also responsible for other diseases, such as asbestosis (fibrosis of the lungs), pleural plaques, thickening and effusions.
结论肺纤维化并非PHT发生的决定因素，但同时合并有肺纤维化的患者预后不良。
Conclusion the incidence of PHT is often latent, and has no relation with disease duration. Pulmonary fibrosis is a very important risk factor for the prognosis of SSc.
前言：目的：从形态学及肺功能研究肺纤维化的形成过程，为治疗肺纤维化提供依据。
Objective: to study the formation of pulmonary fibrosis from morphological and functional aspects and to offer therapy for pulmonary fibrosis.
前言：目的：从形态学及肺功能研究肺纤维化的形成过程，为治疗肺纤维化提供依据。
Objective: to study the formation of pulmonary fibrosis from morphological and functional aspects and to offer therapy for pulmonary fibrosis.
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