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- W2014735280 abstract "Interstitial pulmonary fibrosis (IPF), also known as fibrosing alveolitis, may be defined as a condition characterized by inflammation of the walls of the respiratory airspaces of the lungs that proceeds to fibrosis or the laying down of an excess of connective tissue. Fibrosis need not be present at every stage of the process. The inflammatory response may be granulomatous or nongranulomatous. IPF may be considered a subset of the interstitial lung diseases, which may be defined as inflammation, primarily involving the respiratory airspace walls, that may resolve completely or may go on to fibrosis (Fig 1)." @default.
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- W2014735280 title "Interstitial Pulmonary Fibrosis" @default.
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