Interstitial pulmonary fibrosis is the inflammation of walls of respiratory airspaces of the lungs that proceeds to scarring in the lungs. The inflammation may be granulomatous or nongranulomatous. The treatment for IPH cannot remove scarring that already occurred.
Related Journals of Pulmonary Interstitial Fibrosis
Respiratory journal articles, Respiratory care journal articles, Blood Disorders & Transfusion, Insights in Blood Pressure, Clinical Respiratory: Open Access, Heart Lung and Circulation, Clinical Medicine Insights: Circulatory, Respiratory and Pulmonary Medicine, Respiration and Circulation
Pulmonary & Respiratory Medicine received 1690 citations as per Google Scholar report
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