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Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease

The incidence of congenital lobar overinflation (CLO) is reported at 1 in 20,000–30,000 live births and represents 10% of all congenital lung malformations. The occurrence of concomitant congenital heart disease (CHD) and CLO ranges from 12% to 20%. There are diverging views in the management as to...

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Autor principal: Kylat, Ranjit I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552671/
https://www.ncbi.nlm.nih.gov/pubmed/32872114
http://dx.doi.org/10.3390/children7090113
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author Kylat, Ranjit I.
author_facet Kylat, Ranjit I.
author_sort Kylat, Ranjit I.
collection PubMed
description The incidence of congenital lobar overinflation (CLO) is reported at 1 in 20,000–30,000 live births and represents 10% of all congenital lung malformations. The occurrence of concomitant congenital heart disease (CHD) and CLO ranges from 12% to 20%. There are diverging views in the management as to whether early lobectomy or repair of the cardiac defect, with the assumption that respiratory symptomatology would gradually resolve, or a combined lung and cardiac repair would be the ideal first step in the management. In concomitant CLO and CHD, the surgical decision has to be individualized. Prior to surgical intervention a thorough evaluation may be needed with contrast computed tomography (CT) or magnetic resonance imaging (MRI), bronchoscopy, and if needed cardiac catheterization. CLO improves with management of many left to right shunts and in those with anomalous vessels, but early lobectomy or combined approach may be considered in those symptomatic patients with more complex CHD.
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spelling pubmed-75526712020-10-19 Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease Kylat, Ranjit I. Children (Basel) Case Report The incidence of congenital lobar overinflation (CLO) is reported at 1 in 20,000–30,000 live births and represents 10% of all congenital lung malformations. The occurrence of concomitant congenital heart disease (CHD) and CLO ranges from 12% to 20%. There are diverging views in the management as to whether early lobectomy or repair of the cardiac defect, with the assumption that respiratory symptomatology would gradually resolve, or a combined lung and cardiac repair would be the ideal first step in the management. In concomitant CLO and CHD, the surgical decision has to be individualized. Prior to surgical intervention a thorough evaluation may be needed with contrast computed tomography (CT) or magnetic resonance imaging (MRI), bronchoscopy, and if needed cardiac catheterization. CLO improves with management of many left to right shunts and in those with anomalous vessels, but early lobectomy or combined approach may be considered in those symptomatic patients with more complex CHD. MDPI 2020-08-28 /pmc/articles/PMC7552671/ /pubmed/32872114 http://dx.doi.org/10.3390/children7090113 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Kylat, Ranjit I.
Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title_full Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title_fullStr Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title_full_unstemmed Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title_short Managing Congenital Lobar Overinflation Associated with Congenital Heart Disease
title_sort managing congenital lobar overinflation associated with congenital heart disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552671/
https://www.ncbi.nlm.nih.gov/pubmed/32872114
http://dx.doi.org/10.3390/children7090113
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