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F 1+7/12 yrs CC: cough and mild cyanosis Diffuse pulmonary opacity
Diffuse ground-glass opacity, saving subpleural area
Diffuse interstitial widening
Diffuse interstitial widening due to cellular infiltration
Diffuse interstitial widening, even pattern, due to cellular infiltration and fibrosis
Diffuse interstitial widening, even pattern, due to cellular infiltration and fibrosis Also note intraalveolar macrophages and cholesterol clefts
Diffuse interstitial widening, even pattern, due to cellular infiltration and fibrosis Also note intraalveolar macrophages and and hyperplastic pneumocytes
Inflammatory cell mainly composed of lymphocytes and plasma cells
Inflammatory cells mainly composed of lymphocytes and plasma cells
Interstitial collagen lay down Cellular interstitial pneumonia - interstitial chronic inflammatory cell infiltration - type II pneumocytes hyperplasia - interstitial collagen lay down - intralaveolar macrophages Findings are suggestive of chronic pneumonitis of infancy R/O 1. collagen vascular disease 2. viral infection
Date of download: 9/17/2016 Copyright © 2016 American Medical Association. All rights reserved. From: Demystifying Idiopathic Interstitial Pneumonia Arch.
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