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- The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF). 最可能的诊断是特发性肺纤维化（IPF）。
- Objective: Acute idiopathic pulmonary fibrosis (AIPF) is a rare disease. 目的：急性特发性肺间质纤维化是少见疾病。
- These morphologic changes provide basis for formation of idiopathic pulmonary fibrosis. 上述形态学改变对特发性肺纤维化的形成提供了一些依据。
- Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis. 目的观察特发性肺纤维化的超微结构变化并探讨其发病机理。
- Diagnosis: Idiopathic pulmonary fibrosis, with intralobular interstitial thickening. 诊断：特发性肺纤维化并小叶间质增厚。
- Abstract: Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis. 文摘:目的观察特发性肺纤维化的超微结构变化并探讨其发病机理。
- Conclusions Mutations in the genes encoding telomerase components can appear as familial idiopathic pulmonary fibrosis. 结论：端粒酶组分的编码基因发生突变时，能以家庭性特发性肺纤维变性的形式出现。
- Background Bloemycin(BLM) induced pulmonary fibrosis(BPF) is most widely used animal model for idiopathic pulmonary fibrosis. 博莱霉素(BLM)所致的肺纤维化(BPF)模型是最常用的研究特发性肺纤维化的动物模型。
- Objective To investigate the level of DcR 3 gene expression in peripheral blood mononuclear cells (PBMC) and its relation to idiopathic pulmonary fibrosis (IPF). 目的 探讨外周血单核细胞 (PBMC)中DcR3基因表达水平与特发性肺间质纤维化 (IPF)的关系。
- Idiopathic Pulmonary Fibrosis (IPF), also known as Cryptogenic fibrosing alveolitis, is a chronic progressive interstitial lung disease of unknown cause. 什么是'特发性肺纤维化-慢性间质性肺疾病没有明显原因'?
- UIP associated with progressie systemic sclerosis follows a less progressie course and has a better long term prognosis than UIP associated with idiopathic pulmonary fibrosis. 全身性硬皮病常合并间质性肺炎，进展缓慢，预后好于特发性纤维化伴间质性肺炎。
- UIP associated with progressive systemic sclerosis follows a less progressive course and has a better long term prognosis than UIP associated with idiopathic pulmonary fibrosis. 全身性硬皮病常合并间质性肺炎，进展缓慢，预后好于特发性纤维化伴间质性肺炎。
- 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. 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。
- Lung transplants are a common therapy for many end-stage lung diseases such as chronic obstructive pulmonary disease, cystic fibrosis, pulmonary hypertension, idiopathic pulmonary fibrosis and other diseases. 肺移植是许多终末期肺病的普遍治疗方法，例如慢性阻塞性肺病、性纤维病、动脉高血压、发性肺纤维化等疾病。
- Methods The ET1 activities in the serum and BALF from 10 patients with sarcoidosis, 7 with idiopathic pulmonary fibrosis (IPF) and 8 normal subjects nonsmokers were determined using the radioimmunoassay. 方法利用同位素放射免疫直接测定法，检测10例肺结节病和8例特发性肺纤维化（IPF）患者外周血和支气管肺泡灌洗液（BALF）中内皮素1（ET?1）的活性，并与8名健康非吸烟者进行对照。
- Idiopathic pulmonary fibrosis(IPE) is a chronic inflammatory interstitial lung disease which has no definite pathogeny.The state of disease which has a bad prognosis aggravates continuously. 特发性肺纤维化是一种病因不明的慢性炎症性间质性肺疾病,病情呈持续进展,最终因呼吸衰竭而死亡,预后差。
- idiopathic pulmonary fibrosis (IPF) 特发性肺纤维化
- idiopathic pulmonary fibrosis(IPF) 特发性肺纤维化
- Diffuse idiopathic pulmonary fibrosis 弥漫性特发性肺纤维化
- Keywords Fluimucil;idiopathic pulmonary fibrosis;pulmonary function; 富露施;特发性肺间质纤维化;肺功能;
