Idiopathic Pulmonary Fibrosis - IPF
The most common form of pulmonary fibrosis with unknown cause, characterized by progressive scarring and declining lung function.
Connective Tissue Disease - ILD
Lung fibrosis associated with autoimmune conditions such as rheumatoid arthritis, systemic sclerosis, and lupus.
Sarcoidosis
Inflammatory disease that can cause pulmonary fibrosis through the formation of granulomas in lung tissue.
Occupational Lung Disease
Fibrosis resulting from workplace exposure to silica, asbestos, coal dust, or other harmful particulates.