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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 ...
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.
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 .
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 ...
Deaths. Not reported. Smoking-related interstitial fibrosis (SRIF) is an abnormality in the lungs characterized by excessive collagen deposition within the walls of the air sacs ( interstitial fibrosis ). This abnormality can be seen with a microscope and diagnosed by pathologists. It is caused by cigarette smoking.
Pneumocystis pneumonia ( PCP ), also known as Pneumocystis jirovecii pneumonia ( PJP ), is a form of pneumonia that is caused by the yeast-like fungus Pneumocystis jirovecii. [3] [4] Pneumocystis specimens are commonly found in the lungs of healthy people although it is usually not a cause for disease. [5]
The ICD-10 Clinical Modification ( ICD-10-CM) is a set of diagnosis codes used in the United States of America. [1] It was developed by a component of the U.S. Department of Health and Human services, [2] as an adaption of the ICD-10 with authorization from the World Health Organization. In 2015, ICD-10-CM replaced ICD-9-CM as the federally ...
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 lower lobes of the lungs. [1]