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Adult diagnosis of Swyer-James-MacLeod syndrome: a case report

INTRODUCTION: Swyer-James-MacLeod syndrome or unilateral hyperlucent lung syndrome is a rare entity associated with postinfectious bronchiolitis obliterans occurring in childhood. It is characterized by hypoplasia and/or agenesis of the pulmonary arteries resulting in pulmonary parenchyma hypoperfus...

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Autores principales: Capela, Carlos, Gouveia, Paulo, Sousa, Marco, Regadas, Maria J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023754/
https://www.ncbi.nlm.nih.gov/pubmed/21205288
http://dx.doi.org/10.1186/1752-1947-5-2
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author Capela, Carlos
Gouveia, Paulo
Sousa, Marco
Regadas, Maria J
author_facet Capela, Carlos
Gouveia, Paulo
Sousa, Marco
Regadas, Maria J
author_sort Capela, Carlos
collection PubMed
description INTRODUCTION: Swyer-James-MacLeod syndrome or unilateral hyperlucent lung syndrome is a rare entity associated with postinfectious bronchiolitis obliterans occurring in childhood. It is characterized by hypoplasia and/or agenesis of the pulmonary arteries resulting in pulmonary parenchyma hypoperfusion. CASE PRESENTATION: Here we report the case of a 53-year-old Caucasian woman with Swyer-James-MacLeod syndrome found in the differential diagnosis workup for a new onset of heart failure, secondary to pulmonary arterial hypertension complicated by a patent ductus arteriosus. CONCLUSION: Typically, this disorder is diagnosed in childhood after evaluation for recurrent respiratory infections, but sometimes an indolent course means diagnosis is not made until adulthood.
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spelling pubmed-30237542011-01-20 Adult diagnosis of Swyer-James-MacLeod syndrome: a case report Capela, Carlos Gouveia, Paulo Sousa, Marco Regadas, Maria J J Med Case Reports Case Report INTRODUCTION: Swyer-James-MacLeod syndrome or unilateral hyperlucent lung syndrome is a rare entity associated with postinfectious bronchiolitis obliterans occurring in childhood. It is characterized by hypoplasia and/or agenesis of the pulmonary arteries resulting in pulmonary parenchyma hypoperfusion. CASE PRESENTATION: Here we report the case of a 53-year-old Caucasian woman with Swyer-James-MacLeod syndrome found in the differential diagnosis workup for a new onset of heart failure, secondary to pulmonary arterial hypertension complicated by a patent ductus arteriosus. CONCLUSION: Typically, this disorder is diagnosed in childhood after evaluation for recurrent respiratory infections, but sometimes an indolent course means diagnosis is not made until adulthood. BioMed Central 2011-01-04 /pmc/articles/PMC3023754/ /pubmed/21205288 http://dx.doi.org/10.1186/1752-1947-5-2 Text en Copyright ©2011 Capela et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Capela, Carlos
Gouveia, Paulo
Sousa, Marco
Regadas, Maria J
Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title_full Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title_fullStr Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title_full_unstemmed Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title_short Adult diagnosis of Swyer-James-MacLeod syndrome: a case report
title_sort adult diagnosis of swyer-james-macleod syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023754/
https://www.ncbi.nlm.nih.gov/pubmed/21205288
http://dx.doi.org/10.1186/1752-1947-5-2
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