Pulmonary fibrosis is a condition in which the tissue deep in your lungs becomes scarred over time. This tissue gets thick and stiff. That makes it hard for you to catch your breath, and your blood may not get enough oxygen.
Causes of pulmonary fibrosis include environmental pollutants, some medicines, some connective tissue diseases, and interstitial lung disease. Interstitial lung disease is the name for a large group of diseases that inflame or scar the lungs. In most cases, the cause cannot be found. This is called idiopathic pulmonary fibrosis.
- Shortness of breath
- A dry, hacking cough that doesn't get better
- Weight loss for no known reason
- Aching muscles and joints
- Clubbing, which is the widening and rounding of the tips of the fingers or toes
Your doctor may use your medical history, imaging tests, a biopsy, and lung function tests to diagnose pulmonary fibrosis. There is no cure. Treatments can help with symptoms and improve your quality of life. They include medicines, oxygen therapy, pulmonary rehabilitation, or a lung transplant.
NIH: National Heart, Lung, and Blood Institute
Diagnosis and Tests
- Blood Oxygen Level (National Library of Medicine) Also in Spanish
- Bronchoscopy and Bronchoalveolar Lavage (BAL) (National Library of Medicine) Also in Spanish
- Lung Function Tests (National Library of Medicine) Also in Spanish
- Spirometry (Mayo Foundation for Medical Education and Research)
- Tests for Lung Disease (National Heart, Lung, and Blood Institute) Also in Spanish
- Maintain Your Health (Pulmonary Fibrosis Foundation)
- Pulmonary Rehabilitation: MedlinePlus Health Topic (National Library of Medicine) Also in Spanish
- Familial Pulmonary Fibrosis (National Jewish Health)
- Hermansky-Pudlak syndrome: MedlinePlus Genetics (National Library of Medicine)
- Idiopathic pulmonary fibrosis: MedlinePlus Genetics (National Library of Medicine)
- ClinicalTrials.gov: Pulmonary Fibrosis (National Institutes of Health)
Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine)
- Article: ZC3H4 regulates infiltrating monocytes, attenuating pulmonary fibrosis through IL-10.
- Article: Differences in the characteristics and pulmonary toxicity of nano- and micron-sized...
- Article: Dysfunctional ERG signaling drives pulmonary vascular aging and persistent fibrosis.
- Pulmonary Fibrosis -- see more articles