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.
Farlex Partner Medical Dictionary © Farlex 2012

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.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005
References in periodicals archive ?
Ultrasound in the interstitial pulmonary fibrosis. Can it facilitate a best routine assessment in rheumatic disorders?
Goulet had been suffering from interstitial pulmonary fibrosis and was awaiting a lung transplant.
The PA view of the chest showed increased bibasilar densities, which are compatible with interstitial pulmonary fibrosis (Figure 1).
In contrast, the percentage of transplants going to patients with interstitial pulmonary fibrosis rose from 31% before the scoring system to 44% by last winter.
As a rule, it is self-limiting and resolves without treatment, but some untreated cases may progress to chronic Q fever (endocarditis, granulomatous hepatitis, osteomyelitis, interstitial pulmonary fibrosis) (6).
Strongyloides stercoralis hyperinfection can mimic accelerated idiopathic pulmonary fibrosis.[2] A case of interstitial pulmonary fibrosis and spontaneous pneumothorax associated with Schistosoma haematobium was reported in South Africa.[3] In laboratory settings, Retnla-/- mice developed fibrosis in their lungs after being challenged with Schistosoma mansoni eggs.[4] A variety of cytokines (especially Th2 cytokines), chemokines, and growth factors play important roles in regulating pulmonary fibrosis.
Familial diffuse interstitial pulmonary fibrosis [in French].

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