首页 | 本学科首页   官方微博 | 高级检索  
     

特发性肺纤维化的综合诊断进展
引用本文:左翠云,刘超. 特发性肺纤维化的综合诊断进展[J]. 临床肺科杂志, 2009, 14(4): 458-460
作者姓名:左翠云  刘超
作者单位:蚌埠医学院第一附属医院呼吸内科,安徽,233000;蚌埠医学院第一附属医院呼吸内科,安徽,233000
摘    要:特发性肺纤维化是最常见的一种特发性间质性肺炎,组织病理表现为普通型间质性肺炎,临床表现为进行性呼吸困难伴有刺激性干咳,确诊依赖于外科肺活检。但肺活检风险大、费用高,不易被患者接受。近年来研究发现综合HRCT、血清标志物、以及肺功能、支气管肺泡灌洗液等检查,可以对IPF作出早期准确的诊断。本文将从上述几个方面作一介绍。

关 键 词:特发性肺纤维化  普通型间质性肺炎  诊断

The development in the diagnosis of idiopathic pulmonary fibrosis
ZUO Cui-yun,LIU Chao. The development in the diagnosis of idiopathic pulmonary fibrosis[J]. Journal of Clinical Pulmonary Medicine, 2009, 14(4): 458-460
Authors:ZUO Cui-yun  LIU Chao
Affiliation:ZUO Cui-yun,LIU Chao The Department of Respiratory Medicine,the First Affiliated Hospital of Bengbu Medical College,Bengbu 233000,Anhui Province,China
Abstract:Idiopathic pulmonary fibrosis (IPF) is a most common form of idiopathic interstitial pneumonia, characterized by a histological pattern of usual interstitial pneumonia. Typical symptoms of IPF include chronic progressive exertion breathlessness, frequently accompanied by a non-productive cough.The final diagnosis depended on surgical lung biopsy which has more risk and higher cost, and most patients can not accept it. It is recognized recently that high-resolution computerized topographic scanning (HRCT) co...
Keywords:idiopathic pulmonary fibrosis  usual interstitial pneumonia  diagnosis  
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号