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Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics

Pleuroparenchymal fibroelastosis (PPFE) is a rare pulmonary fibrosis that is clinically characterized by upper-lobe predominant fibrosis. PPFE is a slowly progressive disorder and its first symptom is dyspnea or dry cough. Chest pain because of pneumothorax may be the first symptom in some patients....

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Autor principal: Watanabe, Kentaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933942/
https://www.ncbi.nlm.nih.gov/pubmed/24578677
http://dx.doi.org/10.2174/1573398X0904140129125307
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author Watanabe, Kentaro
author_facet Watanabe, Kentaro
author_sort Watanabe, Kentaro
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description Pleuroparenchymal fibroelastosis (PPFE) is a rare pulmonary fibrosis that is clinically characterized by upper-lobe predominant fibrosis. PPFE is a slowly progressive disorder and its first symptom is dyspnea or dry cough. Chest pain because of pneumothorax may be the first symptom in some patients. Patients with PPFE are slender with a flat rib cage or abnormally narrowed anterior–posterior thoracic dimension. Decreases in forced vital capacity, total lung capacity, and diffusing capacity are respiratory-function characteristics of PPFE, similar to those seen in idiopathic pulmonary fibrosis (IPF). The most remarkable difference in clinical features between PPFE and IPF is imaging findings, with upper-lobe-predominant lesions in PPFE and lower-lobe-predominant lesions in IPF.
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spelling pubmed-39339422014-02-25 Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics Watanabe, Kentaro Curr Respir Med Rev Article Pleuroparenchymal fibroelastosis (PPFE) is a rare pulmonary fibrosis that is clinically characterized by upper-lobe predominant fibrosis. PPFE is a slowly progressive disorder and its first symptom is dyspnea or dry cough. Chest pain because of pneumothorax may be the first symptom in some patients. Patients with PPFE are slender with a flat rib cage or abnormally narrowed anterior–posterior thoracic dimension. Decreases in forced vital capacity, total lung capacity, and diffusing capacity are respiratory-function characteristics of PPFE, similar to those seen in idiopathic pulmonary fibrosis (IPF). The most remarkable difference in clinical features between PPFE and IPF is imaging findings, with upper-lobe-predominant lesions in PPFE and lower-lobe-predominant lesions in IPF. Bentham Science Publishers 2013-08 2013-08 /pmc/articles/PMC3933942/ /pubmed/24578677 http://dx.doi.org/10.2174/1573398X0904140129125307 Text en © 2013 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Watanabe, Kentaro
Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title_full Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title_fullStr Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title_full_unstemmed Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title_short Pleuroparenchymal Fibroelastosis: Its Clinical Characteristics
title_sort pleuroparenchymal fibroelastosis: its clinical characteristics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933942/
https://www.ncbi.nlm.nih.gov/pubmed/24578677
http://dx.doi.org/10.2174/1573398X0904140129125307
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