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Pulmonary fibrosis in children
Authors
N. Nathan Sileo, C. Thouvenin, G. Berdah, L. Delestrain, C. Manali, E. Papiris, S. Léger, P.-L. Le Pointe, H.D. L’Hermine, A.C. Clement, A.
Publication date
1 January 2019
Publisher
Abstract
Pulmonary fibrosis (PF) is a very rare condition in children, which may be observed in specific forms of interstitial lung disease. None of the clinical, radiological, or histological descriptions used for PF diagnosis in adult patients, especially in situations of idiopathic PF, can apply to pediatric situations. This observation supports the view that PF expression may differ with age and, most likely, may cover distinct entities. The present review aims at summarizing the current understanding of PF pathophysiology in children and identifying suitable diagnostic criteria. © 2019 by the authors. Licensee MDPI, Basel, Switzerland
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Pergamos : Unified Institutional Repository / Digital Library Platform of the National and Kapodistrian University of Athens
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Last time updated on 10/02/2023