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Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease

Spontaneous esophageal perforation is a rare and life-threatening disorder. Failure to diagnosis within the first 24-48 hours of presentation portends a poor prognosis. A patient with mixed connective tissue disease (MCTD) on low-dose prednisone and methotrexate presented moribund with chest and sho...

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Detalles Bibliográficos
Autor principal: Lyman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263470/
https://www.ncbi.nlm.nih.gov/pubmed/22279514
http://dx.doi.org/10.2174/1874312901105010138
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author Lyman, David
author_facet Lyman, David
author_sort Lyman, David
collection PubMed
description Spontaneous esophageal perforation is a rare and life-threatening disorder. Failure to diagnosis within the first 24-48 hours of presentation portends a poor prognosis. A patient with mixed connective tissue disease (MCTD) on low-dose prednisone and methotrexate presented moribund with chest and shoulder pain, a left hydropneumothorax, progressive respiratory failure and shock. Initial management focussed on presumed community acquired pneumonia (CAP) in a patient on immunosuppressants. Bilateral yeast empyemas were treated and attributed to immunosuppression. On day 26, the patient developed mediastinitis, and the diagnosis of esophageal perforation was first considered. A review of the literature suggests that the diagnosis and management of spontaneous esophageal perforation could have been more timely and the outcome less catastrophic.
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spelling pubmed-32634702012-01-25 Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease Lyman, David Open Rheumatol J Article Spontaneous esophageal perforation is a rare and life-threatening disorder. Failure to diagnosis within the first 24-48 hours of presentation portends a poor prognosis. A patient with mixed connective tissue disease (MCTD) on low-dose prednisone and methotrexate presented moribund with chest and shoulder pain, a left hydropneumothorax, progressive respiratory failure and shock. Initial management focussed on presumed community acquired pneumonia (CAP) in a patient on immunosuppressants. Bilateral yeast empyemas were treated and attributed to immunosuppression. On day 26, the patient developed mediastinitis, and the diagnosis of esophageal perforation was first considered. A review of the literature suggests that the diagnosis and management of spontaneous esophageal perforation could have been more timely and the outcome less catastrophic. Bentham Open 2011-12-30 /pmc/articles/PMC3263470/ /pubmed/22279514 http://dx.doi.org/10.2174/1874312901105010138 Text en © David Lyman; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Lyman, David
Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title_full Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title_fullStr Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title_full_unstemmed Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title_short Spontaneous Esophageal Perforation in a Patient with Mixed Connective Tissue Disease
title_sort spontaneous esophageal perforation in a patient with mixed connective tissue disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263470/
https://www.ncbi.nlm.nih.gov/pubmed/22279514
http://dx.doi.org/10.2174/1874312901105010138
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