10.3969/j.issn.1005-5185.2008.01.016
特发性肺纤维化的HRCT特点
@@ 特发性肺纤维化(Idiopathic pulmonary fibrosis,IPF)是特发性间质性肺炎(idiopathic interstitial pneumonia,IIP)最常见的临床类型.2002年美国胸科协会(American Thoracic Society,ATS)和欧洲呼吸协会(European Respiratory Society,ERS),将IIP分为以下7种[1]:(1)普通型间质肺炎(Usual interstitial pneuminia,UIP)/特发性肺纤维化(IPF);(2)非特异性间质性肺炎(Nonspecific interstitial pneumonia,NSIP);(3)隐原性机化性肺炎(Cryptogenic organising pneumonia,COP);(4)急性间质性肺炎(Acute interstitial neumonia,AIP);(5)呼吸性细支气管炎伴间质性肺病(Respiratory bronchiolitis-associated interstitial lung disease,RBILD);(6)脱屑性间质性肺炎(Desquamative interstitial pneumonia,DIP);(7)淋巴样间质性肺炎(Lymphoid interstitial pneumonia,LIP).
肺、特发性肺纤维化、HRCT
16
R814.41;R563(放射医学)
2008-06-19(万方平台首次上网日期,不代表论文的发表时间)
共5页
50-54