Diffuse interstitial pulmonary fibrosis was a group of diseases which had the similar morphology and different etiology.
弥漫性肺间质纤维化是一组病因各异，病理形态相似的疾病。
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。
Paraquat poisoning the most common complications are pulmonary interstitial fibrosis, and often it leads to respiratory failure and death.
百草枯中毒最常见的并发症是肺间质纤维化，并常因此导致肺功能衰竭而死亡。
This study shows that pulmonary interstitial fibrosis can be caused by contacting to dust and the pathogenesis needs further research.
这项研究表明粉尘接触可引发肺间质纤维化，其发病机制有待进一步研究。
One died of pulmonary interstitial fibrosis.
死亡原因为肺间质纤维化。
In the follow-up period, among 6 cases accompanied with lung involvement, 3 cases recovered, 2 cases relieved, 1 case died of pulmonary interstitial fibrosis after 3 months.
伴有肺部受累的6例，随访期间，3例恢复正常，2例病情缓解，1例3个月后死于肺间质纤维化。
Pulmonary fibrosis is caused by many factors and shows diffuse interstitial tissue hyperplasia.
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。
OBJECTIVE: To evaluate the effect of N-Mucisol (NAC) on the treatment of acute pulmonary injury and pulmonary interstitial fibrosis.
前言：目的：评价N -乙酰半胱氨酸(NAC)治疗急性肺损伤和肺间质纤维化的作用。
In 80 patients with predominant pulmonary interstitial diseases, thickened BVB with coarse margin or distortion were common in patients with pulmonary fibrosis.
在80例以肺间质为主的病变中，支气管血管束增粗、边缘毛糙、扭曲变形主要见于慢性支气管炎合并间质纤维化及胶原病肺纤维化；
Chest radiograph, and lung CT is diagnostic pulmonary fibrosis, interstitial lung disease most important first step, in this first step also have the misdiagnosis.
胸片和肺部CT是诊断肺纤维化、肺间质病最重要的第一步，在这第一步也有误诊的。
Conclusion: the phosphorylation of RB protein can be induced by hyperoxia. Excessive proliferation of LF leads the pulmonary interstitial fibrosis.
结论：高氧可能导致RB蛋白磷酸化(RB灭活)，LF过度增殖最终导致肺间质纤维化。
Animal experiments performed on dogs and rats have shown mere slight pulmonary interstitial fibrosis.
用狗与大鼠进行实验，可见肺间质纤维组织轻度增生。
Similar to the silicosis, idiopathic pulmonary fibrosis (IPF), which is another lung interstitial disease, is characterized by lung fibrosis.
与矽肺的发病相似，特发性肺纤维化(IPF)也是以肺成纤维细胞大量增殖为主要特征的肺纤维化疾病。
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。
Recent research progress and therapeutic condition of Idiopathic Pulmonary Interstitial Fibrosis(IPIF) were reviewed.
就近来对特发性肺间质纤维化的研究进展及治疗现状进行分析。
Recent research progress and therapeutic condition of Idiopathic Pulmonary Interstitial Fibrosis(IPIF) were reviewed.
就近来对特发性肺间质纤维化的研究进展及治疗现状进行分析。
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