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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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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. |
format | Text |
id | pubmed-3023754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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