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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 .
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.
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 ...
Five years after my chest pain first began, that was the case for me. In 2021, after my second hospitalization and sixth lung collapse, I was diagnosed with thoracic endometriosis, a type of ...
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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