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Vascular anomaly: Cause of infant respiratory distress and dysphagia
Aberrant right subclavian artery with a left aortic arch is rare, but it is the most common congenital aortic arch anomaly. It can present as an incidental finding later in life or be symptomatic at a young age. Here, we describe a case of an aberrant right subclavian artery discovered in a 4 month...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656703/ https://www.ncbi.nlm.nih.gov/pubmed/31367518 http://dx.doi.org/10.1016/j.rmcr.2019.100908 |
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author | Baig, Aisha Fortner, Christopher Rivera, Marcus Merrow, Jill Gupta, Saurabh Sher, Erica Mortelliti, Anthony |
author_facet | Baig, Aisha Fortner, Christopher Rivera, Marcus Merrow, Jill Gupta, Saurabh Sher, Erica Mortelliti, Anthony |
author_sort | Baig, Aisha |
collection | PubMed |
description | Aberrant right subclavian artery with a left aortic arch is rare, but it is the most common congenital aortic arch anomaly. It can present as an incidental finding later in life or be symptomatic at a young age. Here, we describe a case of an aberrant right subclavian artery discovered in a 4 month old with respiratory distress and feeding difficulties. She underwent an extensive aerodigestive evaluation including bronchoscopy, both flexible and rigid, upper GI endoscopy, modified barium swallow with esophageal sweep, chest imaging, CT thorax and echocardiogram. The final decision per the management team was to observe the patient in order to allow more growth. She ultimately improved with age and remains asymptomatic. |
format | Online Article Text |
id | pubmed-6656703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-66567032019-07-31 Vascular anomaly: Cause of infant respiratory distress and dysphagia Baig, Aisha Fortner, Christopher Rivera, Marcus Merrow, Jill Gupta, Saurabh Sher, Erica Mortelliti, Anthony Respir Med Case Rep Case Report Aberrant right subclavian artery with a left aortic arch is rare, but it is the most common congenital aortic arch anomaly. It can present as an incidental finding later in life or be symptomatic at a young age. Here, we describe a case of an aberrant right subclavian artery discovered in a 4 month old with respiratory distress and feeding difficulties. She underwent an extensive aerodigestive evaluation including bronchoscopy, both flexible and rigid, upper GI endoscopy, modified barium swallow with esophageal sweep, chest imaging, CT thorax and echocardiogram. The final decision per the management team was to observe the patient in order to allow more growth. She ultimately improved with age and remains asymptomatic. Elsevier 2019-07-16 /pmc/articles/PMC6656703/ /pubmed/31367518 http://dx.doi.org/10.1016/j.rmcr.2019.100908 Text en © 2019 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Baig, Aisha Fortner, Christopher Rivera, Marcus Merrow, Jill Gupta, Saurabh Sher, Erica Mortelliti, Anthony Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title | Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title_full | Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title_fullStr | Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title_full_unstemmed | Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title_short | Vascular anomaly: Cause of infant respiratory distress and dysphagia |
title_sort | vascular anomaly: cause of infant respiratory distress and dysphagia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656703/ https://www.ncbi.nlm.nih.gov/pubmed/31367518 http://dx.doi.org/10.1016/j.rmcr.2019.100908 |
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