查询词典 pulmonary emphysema

Patients with respiratory diseases, such as chronic bronchitis, emphysema and bronchiectasis pulmonary insufficiency.

呼吸系统疾病患者，如慢性支气管炎、肺气肿以及支气管扩张肺功能不全。

Results Both chest radiography and CT could depicted the size, location and morphology of the giant bulla, but CT could shown the wall and internal condition of bulla, adjacent emphysema, and compression of the normal pulmonary tissue.

结果 胸部X线平片和CT均能清晰显示巨大肺大泡的大小、位置和形态，但是CT还可显示巨大肺大泡的内部情况、肺大泡壁及邻近肺气肿和正常肺组织的受压情况。

Objective To study the window technique in evaluating the chronic obstructive emphysema and pulmonary residual volume in long - term smoker without symptoms.

目的探讨窗技术对慢性阻塞性肺气肿和无症状长期吸烟者肺残气量的评价。

Pleural calcification was missed by chest film but found in 4 by CT. Pleural effusion was noted in 3 by chest film and 4 by CT. HRCT is superior to conventional chest film in demonstrating the changes in the seconday pulmonary lobule such as focal emphysema, interlobular septa thickness and bronchiolar wall thickness.

胸部x光显示肋膜增厚者10例，CT18例，肋膜钙化者无，CT4例，肋膜积水者3例，CT4例，高解像力电脑断层检查更可显示次级肺小叶內的变化如局部气肿，小叶问隔增厚，小支气管壁增厚，这些均优於传统胸部x光片。

The observation was focused on the pulmonary cavitary lesions, interstitial fibrosis, pneumothorax, pneumomediastinum, subcutaneous emphysema and pleural effusion....

结果 根据X线平片和CT所见，在182例患者中，6例(3.3％)出现空洞病变，临床诊断为霉菌感染；10例(5.5％)出现胸水，8例(4.4％)出现纵隔气肿和皮下气肿，3例(1.6％)出现气胸。

It also showed that the injury of endothelia might play certain role in the genesis and development of emphysema and pulmonary hypertension.

由此说明内皮细胞损伤可能在肺气肿、肺动脉高压的发生、发展中起一定作用。

There were 17 thoracic diseases such as emphysema, bullectomy for spontaneous pneumothorax, massive bullae, benign tumor of mediastinum, cyst of mediastinum, pulmonary benign tumors, hydropericardium, malignant pleural fluid, etc.

包括：重度肺气肿、自发性气胸、巨大肺大疱、纵隔良性肿瘤、纵隔囊肿、肺良性肿瘤、心包积液、恶性胸水、肺转移癌、胸膜结核、急性脓胸等17种胸部疾病。

A retrospective multicentre study was conducted in 40 patients (38 males; age 68+/-9 yrs; 39 smokers) with combined pulmonary fibrosis and emphysema, and pulmonary hypertension at right heart catheterisation.

回顾性分析多中心研究的40例（男性38例，年龄68 +/-9岁；吸烟者39例）合并肺间质纤维化和肺气肿，右心导管插入术测量肺动脉高压。

Patients with combined pulmonary fibrosis and emphysema syndrome and pulmonary hypertension confirmed by right heart catheterisation have a dismal prognosis despite moderately altered lung volumes and flows and moderately severe haemodynamic parameters.

尽管适度改变肺容积、血流量、血流动力学参数，合并肺间质纤维化和肺气肿综合征的肺动脉高压患者预后仍较差。

This study aims to describe the haemodynamic and survival characteristics of patients with pulmonary hypertension in the recently individualised syndrome of combined pulmonary fibrosis and emphysema.

本研究旨在描述近来报道的肺动脉高压合并肺间质纤维化和肺气肿患者的血流动力学和生存特征。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。