Combined pulmonary fibrosis and emphysema: an increasingly recognized condition
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Jornal Brasileiro de Pneumologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132014000300304 |
Resumo: | Combined pulmonary fibrosis and emphysema (CPFE) has been increasingly recognized in the literature. Patients with CPFE are usually heavy smokers or former smokers with concomitant lower lobe fibrosis and upper lobe emphysema on chest HRCT scans. They commonly present with severe breathlessness and low DLCO, despite spirometry showing relatively preserved lung volumes. Moderate to severe pulmonary arterial hypertension is common in such patients, who are also at an increased risk of developing lung cancer. Unfortunately, there is currently no effective treatment for CPFE. In this review, we discuss the current knowledge of the pathogenesis, clinical characteristics, and prognostic factors of CPFE. Given that most of the published data on CPFE are based on retrospective analysis, more studies are needed in order to address the role of emphysema and its subtypes; the progression of fibrosis/emphysema and its correlation with inflammation; treatment options; and prognosis. |
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Combined pulmonary fibrosis and emphysema: an increasingly recognized conditionPulmonary fibrosisEmphysemaHypertension, pulmonaryLung diseases, interstitialCombined pulmonary fibrosis and emphysema (CPFE) has been increasingly recognized in the literature. Patients with CPFE are usually heavy smokers or former smokers with concomitant lower lobe fibrosis and upper lobe emphysema on chest HRCT scans. They commonly present with severe breathlessness and low DLCO, despite spirometry showing relatively preserved lung volumes. Moderate to severe pulmonary arterial hypertension is common in such patients, who are also at an increased risk of developing lung cancer. Unfortunately, there is currently no effective treatment for CPFE. In this review, we discuss the current knowledge of the pathogenesis, clinical characteristics, and prognostic factors of CPFE. Given that most of the published data on CPFE are based on retrospective analysis, more studies are needed in order to address the role of emphysema and its subtypes; the progression of fibrosis/emphysema and its correlation with inflammation; treatment options; and prognosis.Sociedade Brasileira de Pneumologia e Tisiologia2014-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132014000300304Jornal Brasileiro de Pneumologia v.40 n.3 2014reponame:Jornal Brasileiro de Pneumologia (Online)instname:Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)instacron:SBPT10.1590/S1806-37132014000300014info:eu-repo/semantics/openAccessDias,Olívia MeiraBaldi,Bruno GuedesCosta,André NathanCarvalho,Carlos Roberto Ribeiroeng2014-07-10T00:00:00Zoai:scielo:S1806-37132014000300304Revistahttp://www.jornaldepneumologia.com.br/default.aspONGhttps://old.scielo.br/oai/scielo-oai.php||jbp@jbp.org.br|| jpneumo@jornaldepneumologia.com.br1806-37561806-3713opendoar:2014-07-10T00:00Jornal Brasileiro de Pneumologia (Online) - Sociedade Brasileira de Pneumologia e Tisiologia (SBPT)false |
dc.title.none.fl_str_mv |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
title |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
spellingShingle |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition Dias,Olívia Meira Pulmonary fibrosis Emphysema Hypertension, pulmonary Lung diseases, interstitial |
title_short |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
title_full |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
title_fullStr |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
title_full_unstemmed |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
title_sort |
Combined pulmonary fibrosis and emphysema: an increasingly recognized condition |
author |
Dias,Olívia Meira |
author_facet |
Dias,Olívia Meira Baldi,Bruno Guedes Costa,André Nathan Carvalho,Carlos Roberto Ribeiro |
author_role |
author |
author2 |
Baldi,Bruno Guedes Costa,André Nathan Carvalho,Carlos Roberto Ribeiro |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Dias,Olívia Meira Baldi,Bruno Guedes Costa,André Nathan Carvalho,Carlos Roberto Ribeiro |
dc.subject.por.fl_str_mv |
Pulmonary fibrosis Emphysema Hypertension, pulmonary Lung diseases, interstitial |
topic |
Pulmonary fibrosis Emphysema Hypertension, pulmonary Lung diseases, interstitial |
description |
Combined pulmonary fibrosis and emphysema (CPFE) has been increasingly recognized in the literature. Patients with CPFE are usually heavy smokers or former smokers with concomitant lower lobe fibrosis and upper lobe emphysema on chest HRCT scans. They commonly present with severe breathlessness and low DLCO, despite spirometry showing relatively preserved lung volumes. Moderate to severe pulmonary arterial hypertension is common in such patients, who are also at an increased risk of developing lung cancer. Unfortunately, there is currently no effective treatment for CPFE. In this review, we discuss the current knowledge of the pathogenesis, clinical characteristics, and prognostic factors of CPFE. Given that most of the published data on CPFE are based on retrospective analysis, more studies are needed in order to address the role of emphysema and its subtypes; the progression of fibrosis/emphysema and its correlation with inflammation; treatment options; and prognosis. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132014000300304 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-37132014000300304 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1806-37132014000300014 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Pneumologia e Tisiologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Pneumologia e Tisiologia |
dc.source.none.fl_str_mv |
Jornal Brasileiro de Pneumologia v.40 n.3 2014 reponame:Jornal Brasileiro de Pneumologia (Online) instname:Sociedade Brasileira de Pneumologia e Tisiologia (SBPT) instacron:SBPT |
instname_str |
Sociedade Brasileira de Pneumologia e Tisiologia (SBPT) |
instacron_str |
SBPT |
institution |
SBPT |
reponame_str |
Jornal Brasileiro de Pneumologia (Online) |
collection |
Jornal Brasileiro de Pneumologia (Online) |
repository.name.fl_str_mv |
Jornal Brasileiro de Pneumologia (Online) - Sociedade Brasileira de Pneumologia e Tisiologia (SBPT) |
repository.mail.fl_str_mv |
||jbp@jbp.org.br|| jpneumo@jornaldepneumologia.com.br |
_version_ |
1750318345929883648 |