interstitial pulmonary fibrosis

Also found in: Acronyms.

in·ter·sti·tial pul·mo·nar·y fi·bro·sis

includes both idiopathic pulmonary fibrosis and pulmonary fibrosis associated with connective tissue disease and other known primary diseases.

interstitial pulmonary fibrosis

A lung disorder involving widespread deposition of fine scar tissue fibrosis. This interferes with oxygenation of the blood and with the release of carbon dioxide. The condition may be caused by long-term irritation by chemical fumes or industrial dusts, but is usually of presumed AUTOIMMUNE origin. There is breathlessness, cough, chest pain and FINGER CLUBBING and progressive deterioration. There is no specific treatment for the established condition, short of lung transplantation.
References in periodicals archive ?
In the past, patients with interstitial pulmonary fibrosis had a disproportionately high rate of death while awaiting a transplant.
A third study focused on patients with interstitial pulmonary fibrosis will be announced later this year.
Patients and family members who have been impacted or diagnosed with COPD, Interstitial Pulmonary Fibrosis or any other lung disease are welcome to the meeting.

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