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Unusual cause of dysphagia

In this case, we describe a unique case of large renal hydronephrosis in a 79-year-old Indian male patient who had initially presented with 3 months of progressive dysphagia and loss of weight. His dysphagia was initially thought to be related to the atypical diagnosis of achalasia and was being con...

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Detalles Bibliográficos
Autores principales: Koh, Dion, Thakur, Udit, Lim, Wei Mou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721079/
https://www.ncbi.nlm.nih.gov/pubmed/31451451
http://dx.doi.org/10.1136/bcr-2018-227610
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author Koh, Dion
Thakur, Udit
Lim, Wei Mou
author_facet Koh, Dion
Thakur, Udit
Lim, Wei Mou
author_sort Koh, Dion
collection PubMed
description In this case, we describe a unique case of large renal hydronephrosis in a 79-year-old Indian male patient who had initially presented with 3 months of progressive dysphagia and loss of weight. His dysphagia was initially thought to be related to the atypical diagnosis of achalasia and was being considered for an elective laparoscopic Heller myotomy. On performing CT of the abdomen, a large renal mass was discovered. However, predicament remained regarding the exact aetiology of this renal mass. This case highlights a tremendously intriguing case of dysphagia with an underlying aetiology that has not been reported elsewhere previously.
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spelling pubmed-67210792019-09-17 Unusual cause of dysphagia Koh, Dion Thakur, Udit Lim, Wei Mou BMJ Case Rep Unusual Association of Diseases/Symptoms In this case, we describe a unique case of large renal hydronephrosis in a 79-year-old Indian male patient who had initially presented with 3 months of progressive dysphagia and loss of weight. His dysphagia was initially thought to be related to the atypical diagnosis of achalasia and was being considered for an elective laparoscopic Heller myotomy. On performing CT of the abdomen, a large renal mass was discovered. However, predicament remained regarding the exact aetiology of this renal mass. This case highlights a tremendously intriguing case of dysphagia with an underlying aetiology that has not been reported elsewhere previously. BMJ Publishing Group 2019-08-26 /pmc/articles/PMC6721079/ /pubmed/31451451 http://dx.doi.org/10.1136/bcr-2018-227610 Text en © BMJ Publishing Group Limited 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Unusual Association of Diseases/Symptoms
Koh, Dion
Thakur, Udit
Lim, Wei Mou
Unusual cause of dysphagia
title Unusual cause of dysphagia
title_full Unusual cause of dysphagia
title_fullStr Unusual cause of dysphagia
title_full_unstemmed Unusual cause of dysphagia
title_short Unusual cause of dysphagia
title_sort unusual cause of dysphagia
topic Unusual Association of Diseases/Symptoms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721079/
https://www.ncbi.nlm.nih.gov/pubmed/31451451
http://dx.doi.org/10.1136/bcr-2018-227610
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