Idiopathic Pulmonary Fibrosis: A Systemic Disease?

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摘要INTRODUCTIONIdiopathic pulmonary fibrosis (IPF) is a specific type of chronic progressive fibrosing interstitial pneumonia associated with a histopathologic pattern of usual interstitial pneumonia.IPF is typically considered to be a lung-limited disorder.Although the primary manifestations of IPF are pulmonary in nature,IPF is increasingly recognized as a systemic disease due to its strong association with comorbidities and complications.

作者单位 Department of Respiratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China ^[1] Department of Respiratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China;Research Unit of Respiratory Disease, Central South University, Changsha, Hunan 410011, China;Diagnosis and Treatment Central of Respiratory Disease, Central South University, Changsha, Hunan 410011, China ^[2]

关键词 Idiopathic Pulmonary Fibrosis Gastroesophageal Reflux Disease Genetics

栏目名称 Ideas and Opinions

DOI 10.4103/0366-6999.213423

发布时间 2017-09-27

基金项目

The study was supported by grants from the National Natural Science Foundation of China the Natural Science Foundation of Hunan Province the National Key Clinical Specialty Construction Projects

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