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Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers

In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity, which comprised centrilobular or paraseptal emphysema in the upper pulmonary lobes, and fibrosis in the lower lobes accompanied by reduced diffused capacity of the lungs for carbon monoxide (DLCO)....

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Autores principales: Hirano, André Carramenha de Góes, Targueta, Eduardo Pelegrineti, Ferraz de Campos, Fernando Peixoto, Martines, João Augusto dos Santos, Andrade, Dafne, Lovisolo, Silvana Maria, Felipe-Silva, Aloisio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507565/
https://www.ncbi.nlm.nih.gov/pubmed/28740835
http://dx.doi.org/10.4322/acr.2017.022
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author Hirano, André Carramenha de Góes
Targueta, Eduardo Pelegrineti
Ferraz de Campos, Fernando Peixoto
Martines, João Augusto dos Santos
Andrade, Dafne
Lovisolo, Silvana Maria
Felipe-Silva, Aloisio
author_facet Hirano, André Carramenha de Góes
Targueta, Eduardo Pelegrineti
Ferraz de Campos, Fernando Peixoto
Martines, João Augusto dos Santos
Andrade, Dafne
Lovisolo, Silvana Maria
Felipe-Silva, Aloisio
author_sort Hirano, André Carramenha de Góes
collection PubMed
description In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity, which comprised centrilobular or paraseptal emphysema in the upper pulmonary lobes, and fibrosis in the lower lobes accompanied by reduced diffused capacity of the lungs for carbon monoxide (DLCO). Recently, the fibrosis associated with the connective tissue disease was also included in the diagnosis of CPFE, although the exposure to tobacco, coal, welding, agrochemical compounds, and tire manufacturing are the most frequent causative agents. This entity characteristically presents reduced DLCO with preserved lung volumes and severe pulmonary hypertension, which is not observed in emphysema and fibrosis alone. We present the case of a 63-year-old woman with a history of heavy tobacco smoking abuse, who developed progressive dyspnea, severe pulmonary hypertension, and cor pulmonale over a 2-year period. She attended the emergency facility several times complaining of worsening dyspnea that was treated as decompensate chronic obstructive pulmonary disease (COPD). The imaging examination showed paraseptal emphysema in the upper pulmonary lobes and fibrosis in the middle and lower lobes. The echo Doppler cardiogram revealed the dilation of the right cardiac chambers and pulmonary hypertension, which was confirmed by pulmonary trunk artery pressure measurement by catheterization. During this period, she was progressively restricted to the minimal activities of daily life and dependent on caregivers. She was brought to the hospital neurologically obtunded, presenting anasarca, and respiratory failure, which led her to death. The autopsy showed signs of pulmonary hypertension and findings of fibrosis and emphysema in the histological examination of the lungs. The authors highlight the importance of the recognition of this entity in case of COPD associated with severe pulmonary hypertension of unknown cause.
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spelling pubmed-55075652017-07-24 Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers Hirano, André Carramenha de Góes Targueta, Eduardo Pelegrineti Ferraz de Campos, Fernando Peixoto Martines, João Augusto dos Santos Andrade, Dafne Lovisolo, Silvana Maria Felipe-Silva, Aloisio Autops Case Rep Article / Autopsy Case Report In 2005, the combined pulmonary fibrosis and emphysema (CPFE) was first defined as a distinct entity, which comprised centrilobular or paraseptal emphysema in the upper pulmonary lobes, and fibrosis in the lower lobes accompanied by reduced diffused capacity of the lungs for carbon monoxide (DLCO). Recently, the fibrosis associated with the connective tissue disease was also included in the diagnosis of CPFE, although the exposure to tobacco, coal, welding, agrochemical compounds, and tire manufacturing are the most frequent causative agents. This entity characteristically presents reduced DLCO with preserved lung volumes and severe pulmonary hypertension, which is not observed in emphysema and fibrosis alone. We present the case of a 63-year-old woman with a history of heavy tobacco smoking abuse, who developed progressive dyspnea, severe pulmonary hypertension, and cor pulmonale over a 2-year period. She attended the emergency facility several times complaining of worsening dyspnea that was treated as decompensate chronic obstructive pulmonary disease (COPD). The imaging examination showed paraseptal emphysema in the upper pulmonary lobes and fibrosis in the middle and lower lobes. The echo Doppler cardiogram revealed the dilation of the right cardiac chambers and pulmonary hypertension, which was confirmed by pulmonary trunk artery pressure measurement by catheterization. During this period, she was progressively restricted to the minimal activities of daily life and dependent on caregivers. She was brought to the hospital neurologically obtunded, presenting anasarca, and respiratory failure, which led her to death. The autopsy showed signs of pulmonary hypertension and findings of fibrosis and emphysema in the histological examination of the lungs. The authors highlight the importance of the recognition of this entity in case of COPD associated with severe pulmonary hypertension of unknown cause. São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2017-06-30 /pmc/articles/PMC5507565/ /pubmed/28740835 http://dx.doi.org/10.4322/acr.2017.022 Text en Autopsy and Case Reports. ISSN 2236-1960. Copyright © 2017. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the article is properly cited.
spellingShingle Article / Autopsy Case Report
Hirano, André Carramenha de Góes
Targueta, Eduardo Pelegrineti
Ferraz de Campos, Fernando Peixoto
Martines, João Augusto dos Santos
Andrade, Dafne
Lovisolo, Silvana Maria
Felipe-Silva, Aloisio
Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title_full Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title_fullStr Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title_full_unstemmed Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title_short Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
title_sort severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers
topic Article / Autopsy Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507565/
https://www.ncbi.nlm.nih.gov/pubmed/28740835
http://dx.doi.org/10.4322/acr.2017.022
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