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Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology
BACKGROUND: Esophageal duplication cysts are rare congenital tumors usually diagnosed and treated during childhood. Most of them are located in the mediastinum and appear as a mass besides the esophagus. Unfortunately, symptoms are non-specific and depend on the size and location of the mass; theref...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373318/ https://www.ncbi.nlm.nih.gov/pubmed/37496023 http://dx.doi.org/10.1186/s13019-023-02308-z |
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author | Endara, Santiago A. Pinto, Jaime R. Torres, Gustavo A. Arias, Pablo A. Ponton, M. Patricia Molina, Gabriel A. |
author_facet | Endara, Santiago A. Pinto, Jaime R. Torres, Gustavo A. Arias, Pablo A. Ponton, M. Patricia Molina, Gabriel A. |
author_sort | Endara, Santiago A. |
collection | PubMed |
description | BACKGROUND: Esophageal duplication cysts are rare congenital tumors usually diagnosed and treated during childhood. Most of them are located in the mediastinum and appear as a mass besides the esophagus. Unfortunately, symptoms are non-specific and depend on the size and location of the mass; therefore, they can easily be missed. If symptoms appear, surgical resection is necessary to prevent troublesome complications. CASE PRESENTATION: We present the case of a 60-year-old woman who presented with severe progressive dysphagia and epigastric pain. After further evaluation, a paraesophageal cystic mass was found, and surgery was required. Non-communicating esophageal duplication cyst was the final diagnosis. CONCLUSION: Esophageal duplication cysts are a rare pathology in adults; their symptoms will vary depending on their size and location. Preoperative diagnosis is difficult as symptoms are non-specific and can be missed. If severe dysphagia, pain, or any other complication appears, surgery should not be delayed. |
format | Online Article Text |
id | pubmed-10373318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103733182023-07-28 Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology Endara, Santiago A. Pinto, Jaime R. Torres, Gustavo A. Arias, Pablo A. Ponton, M. Patricia Molina, Gabriel A. J Cardiothorac Surg Case Report BACKGROUND: Esophageal duplication cysts are rare congenital tumors usually diagnosed and treated during childhood. Most of them are located in the mediastinum and appear as a mass besides the esophagus. Unfortunately, symptoms are non-specific and depend on the size and location of the mass; therefore, they can easily be missed. If symptoms appear, surgical resection is necessary to prevent troublesome complications. CASE PRESENTATION: We present the case of a 60-year-old woman who presented with severe progressive dysphagia and epigastric pain. After further evaluation, a paraesophageal cystic mass was found, and surgery was required. Non-communicating esophageal duplication cyst was the final diagnosis. CONCLUSION: Esophageal duplication cysts are a rare pathology in adults; their symptoms will vary depending on their size and location. Preoperative diagnosis is difficult as symptoms are non-specific and can be missed. If severe dysphagia, pain, or any other complication appears, surgery should not be delayed. BioMed Central 2023-07-26 /pmc/articles/PMC10373318/ /pubmed/37496023 http://dx.doi.org/10.1186/s13019-023-02308-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Endara, Santiago A. Pinto, Jaime R. Torres, Gustavo A. Arias, Pablo A. Ponton, M. Patricia Molina, Gabriel A. Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title | Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title_full | Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title_fullStr | Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title_full_unstemmed | Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title_short | Severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
title_sort | severe dysphagia due to an esophageal duplication cyst in sixth decade, unusual presentation of a rare pathology |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373318/ https://www.ncbi.nlm.nih.gov/pubmed/37496023 http://dx.doi.org/10.1186/s13019-023-02308-z |
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