id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
cord-016947-8f22ukjc	Mueller-Mang, Christina	Interstitial Lung Diseases	2017-08-24		.txt	text/plain	11260	619	39	The term idiopathic interstitial pneumonias refers to a group of seven entities with distinct histologic patterns: idiopathic pulmonary fibrosis (IPF), characterized by the pattern of usual interstitial pneumonia (UIP); nonspecific interstitial pneumonia (NSIP); cryptogenic organizing pneumonia (COP); respiratory bronchiolitis-associated interstitial lung disease (RB-ILD); desquamative interstitial pneumonia (DIP); lymphoid interstitial pneumonia (LIP); and acute interstitial pneumonia (AIP). In contrast to the heterogeneous lung involvement and the typical a b Fig. 6 (a, b) Axial CT image in a 63-year-old man with usual interstitial pneumonia (UIP)/idiopathic pulmonary fibrosis (IPF) shows bilateral reticular opacities, honeycombing (black arrowheads), and traction bronchiectasis (arrow). In UIP (right) the lung abnormalities show a typical apico-basal gradient with predominance of honeycombing Fig. 9 HRCT shows characteristic subpleural sparing of reticular opacities (arrows) in a 67-year-old patient with NSIP and alveoli, with preservation of the lung architecture.	./cache/cord-016947-8f22ukjc.txt	./txt/cord-016947-8f22ukjc.txt