Diagnostic criteria for idiopathic pulmonary fibrosis

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Diagnostic criteria for idiopathic pulmonary fibrosis Lee Fidler, Shane Shapera The Lancet Respiratory Medicine Volume 6, Issue 2, (February 2018) DOI: 10.1016/S2213-2600(18)30020-1 Copyright © 2018 Elsevier Ltd Terms and Conditions

Figure Proposed framework for categorising CT imaging in the evaluation of IPF Adapted from Lynch and colleagues’ Review.1 The colour gradient represents heterogeneity within each radiographic category. UIP= usual interstitial pneumonia. IPF=idiopathic pulmonary fibrosis. *Reticular pattern is superimposed on ground glass opacity, and in these cases it is usually fibrotic. Pure ground glass opacity, however, would be against the diagnosis of UIP or IPF and would suggest acute exacerbation, hypersensitivity pneumonitis, or other conditions. † Features that are more suggestive of a non-IPF diagnosis. The Lancet Respiratory Medicine 2018 6, DOI: (10.1016/S2213-2600(18)30020-1) Copyright © 2018 Elsevier Ltd Terms and Conditions