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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...

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Autores principales: Endara, Santiago A., Pinto, Jaime R., Torres, Gustavo A., Arias, Pablo A., Ponton, M. Patricia, Molina, Gabriel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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.
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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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