特发性肺纤维化(Idiopathic Pulmonary Fibrosis)是一种原因不明且致死率高的肺间质性肺炎，通常特征会有肺上皮细胞的损伤、肺水肿、免疫细胞的浸润、纤维母细胞的增生以及肺纤维...
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特收性肺纤维化(idiopathicpulmonaryfibrosis，IPF)是一种缘由不明、以洋溢性肺泡炎和肺泡构造杂治最末致使肺间量纤维化为特点的疾病，按病程有急性、亚急性和...
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特发性肺纤维化 Idiopathic Pulmonary Fibrosis ; IPF ; idiopathic pulmonary fibrothersis ; idiopathelloc pulmonary fibrosis
慢性肺纤维化 chronic pulmonary fibrosis
小儿特发性肺纤维化 idiopathic pulmonary fibrosis
放射性肺纤维化 radiation pulmonary fibrosis
家族性肺纤维化症 familiar pulmonary fibrosis
老年人特发性肺纤维化 senile idiopathic pulmonary interstitial fibrosis
间质性肺纤维化 Interstitial pulmonary fibrosis
囊性肺纤维化 Cystic pulmonary fibrosis
发性肺纤维化 idiopathic pulmonary fibrosis ; IPF
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.
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