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Causes. It has been suggested that idiopathic nonspecific interstitial pneumonia has an autoimmune mechanism, and is a possible complication of undifferentiated connective tissue disease; [2] however, not enough research has been done at this time to find a cause. Patients with NSIP will often have other unrelated lung diseases like COPD or ...
Life expectancy with interstitial lung disease can vary greatly. The most common form of interstitial lung disease, idiopathic pulmonary fibrosis (IPF), has a life expectancy of approximately 3 to ...
Specialty. Respirology. Usual interstitial pneumonia ( UIP) is a form of lung disease characterized by progressive scarring of both lungs. [1] The scarring ( fibrosis) involves the pulmonary interstitium (the supporting framework of the lung). UIP is thus classified as a form of interstitial lung disease .
Idiopathic interstitial pneumonia ( IIP ), or noninfectious pneumonia [1] are a class of diffuse lung diseases. These diseases typically affect the pulmonary interstitium, although some also have a component affecting the airways (for instance, cryptogenic organizing pneumonitis ). There are seven recognized distinct subtypes of IIP.
WebMD explains various types of interstitial lung disease. Learn more about the symptoms, causes, diagnosis, treatment, risks, and complications of ILD.
Symptoms of End-Stage COPD. Many of the symptoms you had in earlier stages, like coughing, mucus, shortness of breath, and tiredness, are likely to get worse. Just breathing takes a lot of effort ...
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