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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 ...
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 .
Respirology. 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.
Interstitial lung disease ( ILD ), or diffuse parenchymal lung disease ( DPLD ), [3] is a group of respiratory diseases affecting the interstitium (the tissue) and space around the alveoli (air sacs) of the lungs. [4] It concerns alveolar epithelium, pulmonary capillary endothelium, basement membrane, and perivascular and perilymphatic tissues.
Desquamative interstitial pneumonia. Desquamative interstitial pneumonia (DIP) is a form of idiopathic interstitial pneumonia featuring elevated numbers of macrophages within the alveoli (air sacs) of the lung. The alveolar macrophages have a characteristic light brown pigmentation and accumulate in the alveolar lumen and septa regions of the ...
Life expectancy ~ 4 years [1] Frequency. 12 per 100,000 people per year [4] Idiopathic pulmonary fibrosis ( IPF ), or (formerly [5]) fibrosing alveolitis, is a rare, progressive illness of the respiratory system, characterized by the thickening and stiffening of lung tissue, associated with the formation of scar tissue.
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