慢性阻塞性肺疾病合并肺间质纤维化20例临床分析

    Clinical analysis of chronic obstructive pulmonary disease with pulmonary interstitial fibrosis

    • 摘要: 目的:探讨慢性阻塞性肺疾病(COPD)合并肺间质纤维化(PIF)的临床特点。方法:对20例COPD合并PIF患者的症状、体征、胸部X线片、胸部高分辨率CT(HRCT)、血气分析和肺功能进行回顾性分析,并与COPD未合并PIF患者进行比较。结果:与COPD未合并PIF患者比较,COPD合并PIF患者临床多表现为肺部Velcro罗音(P0.01),肺弥散功能显著降低(P0.01),胸部X线片显示弥漫点状结节状影、网格状蜂窝状影较多(P0.01),HRCT显示毛玻璃状网格状点状影蜂窝肺较多(P0.01)。结论:COPD合并PIF由于双重的病理损害造成肺通气功能、弥散功能严重障碍和严重低氧血症,影响COPD患者的预后。胸部HRCT能为临床提供重要的诊断依据。

       

      Abstract: Objective:To explore the clinical characteristics of chronic obstructive pulmonary disease(COPD) with pulmonary interstial fibrosis(PIF).Methods:The data of clinical symptoms,radiographic features,high resolution computerized tomography(HRCT) of the chest,arterial blood gas analysis and lung function test of 20 cases with COPD and PIF were analyzed retrospectively,and compared with COPD patients.Results:Compared with COPD patients,the clinical features of the patients with COPD and PIF were lung Velcro rale,lung dispersion function decreased,chest X-ray showed diffuse pitting nodular shadows mainly for mesh shape honeycomb shadow(P0.01),and HRCT showed most frosted glass shape and mesh shape pitting shadow honeycomb lung(P0.01).Conclusions:The COPD and PIF damage the ventilation and diffusion function of pulmonary,which can lead to severe hypoxemia and affect prognosis.The HRCT of the chest can provide important evidence in clinical diagnosis.

       

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