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Idiopathic Pulmonary Fibrosis

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Definition: A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.  do not confuse with PULMONARY FIBROSIS    Other names Usual Interstitial Pneumonias; Pulmonary Fibrosis, Idiopathic; Pulmonary Fibroses, Idiopathic; Interstitial Pneumonias, Usual; Interstitial Pneumonia, Usual; Idiopathic Pulmonary Fibroses; Fibrosing Alveolitis, Cryptogenic; Fibrosing Alveolitides, Cryptogenic; Cryptogenic Fibrosing Alveolitides; Usual Interstitial Pneumonia; Cryptogenic Fibrosing Alveolitis
 
SubstanceCAS Registry & nameCategoriesSource
Hamman-Rich disease  0   *Idiopathic Pulmonary Fibrosis.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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