Idiopathic Pulmonary Fibrosis: Unmasking Cryptogenic Environmental Factors
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2019/02/21
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Description:Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease of unknown origin that is associated with high morbidity and mortality. In this perspective, we briefly review the current understanding of the pathophysiology of IPF and the importance of environmental triggers as a precipitant of disease. We discuss occult intrinsic and extrinsic environmental factors that affect the lung microenvironment and may contribute to the development and progression of disease. The clinical implications of this framework need to be further elucidated, because prompt identification and elimination of occult exposures may represent a novel treatment modality. [Description provided by NIOSH]
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ISSN:0903-1936
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Volume:53
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Issue:2
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NIOSHTIC Number:nn:20063869
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Citation:Eur Respir J 2019 Feb; 53(2):1801699
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Contact Point Address:Ganesh Raghu, Center for Interstitial Lung Disease, University of Washington, Seattle, WA 98195, USA
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Email:graghu@uw.edu
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Federal Fiscal Year:2019
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Performing Organization:University of Washington
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:European Respiratory Journal
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End Date:20250630
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Main Document Checksum:urn:sha-512:b30f41fc55bdba0b90f44934e921ba8f9872b5d65ea0ecbad5830db4a8eb735572786034a9b26e28de518dcf946e556795c4a10a8f712fdaf9cdcdf84ac89d9f
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