首页> 美国卫生研究院文献>World Journal of Radiology >Pulmonary fibrosis and emphysema: Is the emphysema type associated with the pattern of fibrosis?
【2h】

Pulmonary fibrosis and emphysema: Is the emphysema type associated with the pattern of fibrosis?

机译:肺纤维化和肺气肿:肺气肿的类型与纤维化的模式有关吗?

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

AIM: To investigate whether the predominant emphysema type is associated with the high resolution computed tomography (HRCT) pattern of fibrosis in combined pulmonary fibrosis and emphysema (CPFE).METHODS: Fifty-three smokers with upper lobe emphysema and lower lobe pulmonary fibrosis on - HRCT - were retrospectively evaluated. Patients were stratified into 3 groups according to the predominant type of emphysema: Centrilobular (CLE), paraseptal (PSE), CLE = PSE. Patients were also stratified into 3 other groups according to the predominant type of fibrosis on HRCT: Typical usual interstitial pneumonia (UIP), probable UIP and nonspecific interstitial pneumonia (NSIP). HRCTs were scored at 5 predetermined levels for the coarseness of fibrosis (Coarseness), extent of emphysema (emphysema), extent of interstitial lung disease (TotExtILD), extent of reticular pattern not otherwise specified (RetNOS), extent of ground glass opacity with traction bronchiectasis (extGGOBx), extent of pure ground glass opacity and extent of honeycombing. HRCT mean scores, pulmonary function tests, diffusion capacity (DLCO) and systolic pulmonary arterial pressure were compared among the groups.RESULTS: The predominant type of emphysema was strongly correlated with the predominant type of fibrosis. The centrilobular emphysema group exhibited a significantly higher extent of emphysema (P < 0.001) and a lower extent of interstitial lung disease (P < 0.002), reticular pattern not otherwise specified (P < 0.023), extent of ground glass opacity with traction bronchiectasis (P < 0.002), extent of honeycombing (P < 0.001) and coarseness of fibrosis (P < 0.001) than the paraseptal group. The NSIP group exhibited a significantly higher extent of emphysema (P < 0.05), total lung capacity (P < 0.01) and diffusion capacity (DLCO) (P < 0.05) than the typical UIP group. The typical UIP group exhibited a significantly higher extent of interstitial lung disease, extent of reticular pattern not otherwise specified, extent of ground glass opacity with traction bronchiectasis, extent of honeycombing and coarseness of fibrosis (0.039 > P > 0.000). Although the pulmonary arterial pressure was higher in typical UIP group relative to the NSIP group, the difference was not statistically significant.CONCLUSION: In CPFE patients, paraseptal emphysema is associated more with UIP-HRCT pattern and higher extent of fibrosis than centrilobular emphysema.
机译:目的:探讨肺气肿的主要类型是否与肺纤维化合并肺气肿(CPFE)的高分辨计算机断层扫描(HRCT)纤维化类型有关。方法:53名吸烟者患有上叶肺气肿和下叶肺纤维化- HRCT-进行回顾性评估。根据主要的肺气肿类型将患者分为三组:中央小叶(CLE),隔中隔(PSE),CLE = PSE。根据HRCT上纤维化的主要类型,患者也分为3组:典型的普通间质性肺炎(UIP),可能的UIP和非特异性间质性肺炎(NSIP)。对HRCT进行5个预定级别的评分,包括纤维化的粗糙程度(粗度),肺气肿的程度(肺气肿),间质性肺病的程度(TotExtILD),网状图案的程度(RetNOS),带牵引力的毛玻璃样不透明程度支气管扩张(extGGOBx),纯毛玻璃不透明程度和蜂窝状程度。比较各组的HRCT平均评分,肺功能测试,弥散能力(DLCO)和收缩期肺动脉压。结果:肺气肿的主要类型与纤维化的主要类型密切相关。小叶肺气肿组表现出明显较高的肺气肿程度(P <0.001)和较低的间质性肺疾病程度(P <0.002),网状模式未另作说明(P <0.023),毛玻璃样混浊伴牵引性支气管扩张(P P <0.002),蜂窝程度(P <0.001)和纤维化粗度(P <0.001)高于隔隔组。与典型的UIP组相比,NSIP组表现出明显更高的肺气肿程度(P <0.05),总肺容量(P <0.01)和扩散容量(DLCO)(P <0.05)。典型的UIP组表现出明显更高的间质性肺疾病范围,网状模式的范围,另有说明,网状玻璃混浊程度及牵引性支气管扩张,蜂窝状程度和纤维化程度(0.039> P> 0.000)。尽管典型的UIP组的肺动脉压相对于NSIP组更高,但差异无统计学意义。结论:在CPFE患者中,隔中肺气肿与UIP-HRCT模式相关,并且纤维化程度高于小叶性肺气肿。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号