Major Categories of Alveolar and Interstitial Inflammatory Lung Disease | |
Lung response: Alveolitis, interstitial inflammation, and fibrosis | |
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Known Cause | |
Asbestos | Radiation |
Aspiration pneumonia | |
Drugs (e.g., nitrofurantoin, amiodarone, methotrexate, rituximab) and chemotherapy drugs | Residual of adult respiratory distress syndrome |
Smoking-related Desquamative interstitial pneumonia Respiratory bronchiolitis-associated interstitial lung disease Langerhans cell granulomatosis (eosinophilic granulomatosis of the lung) | |
Unknown Cause | |
Idiopathic interstitial pneumonias | Pulmonary alveolar proteinosis |
Idiopathic pulmonary fibrosis (usual interstitial pneumonia) | Lymphocytic infiltrative disorders (lymphocytic interstitial pneumonitis associated with connective tissue disease) |
Eosinophilic pneumonias | |
Acute interstitial pneumonia (diffuse alveolar damage) | Lymphangioleiomyomatosis
Amyloidosis |
Cryptogenic organizing pneumonia (bronchiolitis obliterans with organizing pneumonia) Nonspecific interstitial pneumonia | Inherited diseases Tuberous sclerosis, neurofibromatosis, Niemann-Pick disease, Gaucher disease, Hermansky-Pudlak syndrome |
Connective tissue diseases Systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis, Sjögren syndrome, polymyositis-dermatomyositis | Gastrointestinal or liver diseases (Crohn disease, primary biliary cirrhosis, chronic active hepatitis, ulcerative colitis)
Graft-versus-host disease (bone marrow transplantation; solid organ transplantation) |
Pulmonary hemorrhage syndromes Goodpasture syndrome, idiopathic pulmonary hemosiderosis, isolated pulmonary capillaritis | |
Lung response: Granulomatous | |
Known Cause | |
Hypersensitivity pneumonitis (organic dusts) | Inorganic dusts: beryllium, silica |
Unknown Cause | |
Sarcoidosis | Bronchocentric granulomatosis |
Granulomatous vasculitides | Lymphomatoid granulomatosis |
Granulomatosis with polyangiitis (Wegener's), allergic granulomatosis of Churg-Strauss |