从肺胃相关探讨特发性肺纤维化合并胃食管反流的发病机制及其防治  

Discussion on the Pathogenesis of Idiopathic Pulmonary Fibrosis Combined Gastroesophageal Reflux and Its Prevention and Control from the Lung and Stomach Related Theory

作　　者：刘晓莹[1] 张伟[2] 

机构地区：[1]山东中医药大学,山东济南250014 [2]山东中医药大学附属医院肺病科,山东济南250011

出　　处：《湖北中医药大学学报》2016年第3期65-67,共3页Journal of Hubei University of Chinese Medicine

基　　金：山东省人民政府“泰山学者”建设工程专项经费资助(项目编号:ts20110819)

摘　　要：特发性肺纤维化合并胃食管反流病程较长,预后困难,对人体的生命健康构成威胁。阐明肺纤维化形成机制,对于更好地了解其发生、发展和防治显得尤为重要。从肺胃相关理论着手,探讨特发性肺纤维化合并胃食管反流的病机与肺、胃有关,治疗该病可采用肺胃同治的方法。Idiopathic pulmonary fibrosis（ IPF） combined gastroesophageal reflux（ GERD） is a disease with long duration,poor grognosis and posing a threat to human life and health. Therefore,to clarify the formation mechanism of IPF is particularly important to better understand its occurrence,development,prevention and control. The lung and stomach related theory was used to explore the pathogenesis of IPF,the combination of GERD and its prevention and control.

关 键 词：特发性肺纤维化 胃食管反流 发病机制 肺胃同治 

分 类 号：R259[医药卫生—中西医结合]