pulmonary fibrosis

A stain highlights the collagenous connective tissue of pulmonary fibrosis in blue.

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.

Idiopathic pulmonary fibrosis: acting or waiting?

特发性肺纤维化: 治疗还是等待?

Objective : To report a case of single lung transplantation in therapy of end-stage pulmonary fibrosis.

目的报告山东省首例单肺移植术治疗终末期肺纤维化.

Objective : To explore the effect and molecular mechanism of Qidankeli in the treatment of pulmonary fibrosis.

目的探讨芪丹颗粒治疗肺间质纤维化的效果及分子作用机制.

Experimental Study of Pulmonary Fibrosis Disease by Hua Xian Jiao Nang

化纤胶囊治疗肺间质纤维化的实验研究

Objective To evaluate the effect of dipyridamole ( DPM ) and adenosine ( ADO ) on interstitial pulmonary fibrosis in mice.

目的　通过腺苷 ( ADO ) 受体拮抗剂茶碱(TH),探讨ADO、双哌达莫 ( DPM ) 对小鼠肺间质纤维化过程的干预作用.

There was statistical significance of moist rales 、 tubbiness thorax 、 lung boundary descend ( P < 0.05); Results: ( 1) Clinical characteristics of PF-COPD were between COPD and pulmonary fibrosis.

结果：（1）PF-COPD的临床表现介于上述两种疾病之间。双肺湿罗音、桶状胸、肺界下移、肺心病体征2组差异有统计学意义（p<0.05）；

Pulmonary fibrosis is an important toxic effect of paraquat.

在各种肺组织损伤中又以肺纤维化损伤最为突出.

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.

The X-ray changes of 10 cases of pathologically proved cryptogenic diffuse interstitial pulmonary fibrosis are reported.

本文报道经肺活检证实的10例隐原性弥漫性肺间质纤维化的X线改变。

Rationale: Idiopathic pulmonary fibrosis ( IPF), which is the most common idiopathic interstitial lung disease, has the worse prognosis, with a median survival of only 3 to 4 years.

研究背景与目的：特发性肺纤维化（IPF）是特发性间质性肺疾病最常见的类型，其预后差，生存中位时间仅为3至4年。

Only about 1 % of such persons get a significant degree of pulmonary fibrosis.

仅有大约1%的这种病人出现明显的肺纤维化.

Methods Thirty-six male ICR mice were randomized as a negative control ( NC) group and pulmonary fibrosis model ( FM) groups ( FMA, FMB, FMC, FMD, FME sub-groups).

方法36只雄性ICR小鼠，按随机数字表法分为阴性对照组（NC组）和肺纤维化模型组（FMA、FMB、FMC、FMD、FME组），每组6只。

Radiation-induced lung injury ( radio-pulmonary lesion, RPI) is one of the common complications of the chest tumor radiotherapy, patients usually has two kinds of forms, early stage of acute radiation pneumonia and later stage of radiation pulmonary fibrosis.

放射性肺损伤（radio-pulmonary lesion，RPI）是胸部肿瘤放射治疗最为常见并发症之一，临床上通常有两种表现形式，早期急性放射性肺炎和后期放射性肺纤维化[1]。

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 Study the effects and feasibility of life quality list for idiopathic pulmonary fibrosis ( IPF) patients.

目的：探讨研究特发性肺纤维化患者的生存质量评价体系，评估生存质量测评表对特发性肺纤维化患者评价的可行性。

Objective To study the role of matrix metalloproteinase-2 ( MMP 2 ) in rat pulmonary fibrosis.

目的　研究基质金属蛋白酶2 ( MMP2 ) 在肺纤维化中的作用.

At the provincial hospital diagnosis of systemic sclerosis with pulmonary fibrosis.

在省医院住院诊断为系统性硬化症合并肺间质纤维化.

Effects of Different Doses of Atorvastatin on Pulmonary Fibrosis of Rats

不同剂量阿托伐他汀对肺纤维化大鼠的治疗作用

Late findings(≥ 14d) were pulmonary fibrosis and microcyst formation.

晚期（≥14d）则以肺间质纤维化和肺小囊性变多见。

Oxidative stress plays a crucial role during the occurrence of many diseases, such as heart diseases, idiopathic pulmonary fibrosis, falling sickness, and neurodegenerative diseases.

氧化应激在很多疾病的发生中都扮演了重要角色，如心脑血管疾病，特发性肺纤维化，癫痫，神经退行性疾病等等。

Conclusion: BTD is of great benefit to the treatment for pulmonary fibrosis.

结论：补气通肺汤可抑制肺纤维化。

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.

Idiopathic pulmonary fibrosis ( IPF ) has a poor prognosis and a course that is unpredictable.

特 发性 肺纤维化预后不佳,其发展过程无法预知.

Idiopathic pulmonary fibrosis ( IPF) has a poor prognosis and a course that is unpredictable.

特发性肺纤维化预后不佳，其发展过程无法预知。

This experiment is to investigate the effect of IL-10 on bleomycin-induced pulmonary fibrosis in rats by administrating exogenic IL-10 at its different stages.

本研究旨在通过不同时期运用外源性IL-10对博来霉素诱导的肺纤维化大鼠进行干预，探讨外源性IL-10对肺纤维化的作用机理。

Objective To explore whether ammonium perchlorate ( AP ) could cause animal pulmonary fibrosis.

探讨过氯酸铵 ( AP ) 致动物肺纤维化作用.

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.

Interstitial pulmonary fibrosis in association with dermatomyositis: Report of 5 cases

皮肌炎并发间质性肺纤维化5例报告

Objective To study high-resolution CT ( HRCT) diagnosis and differential diagnosis of idiopathic pulmonary fibrosis ( IPF).

目的探讨高分辨率CT（HRCT）对特发性肺纤维化（IPF）的诊断及鉴别诊断的价值。