How to treat interstitial pneumonia in the late stage of interstitial pneumonia? How long can you live?

Classification of main interstitial lung diseases At present, ILD/DPLD can be divided into four categories internationally: ① DPLD with known etiology, such as pulmonary manifestations of drug-induced, occupational or environmentally harmful substances (beryllium and asbestos) DPLD or collagen angiopathy; Zhang Wei, Department of Pulmonary Diseases, Affiliated Hospital of Shandong University of Traditional Chinese Medicine ② Idiopathic interstitial pneumonia (IIP) includes seven clinicopathological types: idiopathic pulmonary fibrosis (IPF)/ interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP), cryptogenic organizing pneumonia (COP)/ organized pneumonia (OP), acute interstitial pneumonia (AIP)/ diffuse alveolar injury (DAD). ③ Granulomatous DPLD, such as sarcoidosis, exogenous allergic alveolitis and Wegener granuloma; ④ Other rare DPLD, such as pulmonary alveolar proteinosis, pulmonary hemorrhage-nephritis syndrome, pulmonary lymphangioleiomyomatosis, Langerhans cell histiocytosis, chronic eosinophilic pneumonia and idiopathic pulmonary hemosiderosis. View original post >>