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An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis
Cricopharyngeal (CP) dysfunction is a frequent cause of dysphagia among patients with inclusion body myositis. Early identification and prompt treatment is necessary because aspiration pneumonia is a leading cause of mortality among these patients. We present a case of a 57-year-old woman with a his...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621890/ https://www.ncbi.nlm.nih.gov/pubmed/37928231 http://dx.doi.org/10.14309/crj.0000000000001194 |
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author | Ramirez Ramirez, Oscar A. Hillman, Luke |
author_facet | Ramirez Ramirez, Oscar A. Hillman, Luke |
author_sort | Ramirez Ramirez, Oscar A. |
collection | PubMed |
description | Cricopharyngeal (CP) dysfunction is a frequent cause of dysphagia among patients with inclusion body myositis. Early identification and prompt treatment is necessary because aspiration pneumonia is a leading cause of mortality among these patients. We present a case of a 57-year-old woman with a history of inclusion body myositis who presented with progressive dysphagia and aspiration pneumonia found to have CP dysfunction treated with endoscopic CP myotomy. Postoperatively, patient's dysphagia improved with no further episodes of aspiration at 2-year follow-up. |
format | Online Article Text |
id | pubmed-10621890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-106218902023-11-03 An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis Ramirez Ramirez, Oscar A. Hillman, Luke ACG Case Rep J Case Report Cricopharyngeal (CP) dysfunction is a frequent cause of dysphagia among patients with inclusion body myositis. Early identification and prompt treatment is necessary because aspiration pneumonia is a leading cause of mortality among these patients. We present a case of a 57-year-old woman with a history of inclusion body myositis who presented with progressive dysphagia and aspiration pneumonia found to have CP dysfunction treated with endoscopic CP myotomy. Postoperatively, patient's dysphagia improved with no further episodes of aspiration at 2-year follow-up. Wolters Kluwer 2023-11-02 /pmc/articles/PMC10621890/ /pubmed/37928231 http://dx.doi.org/10.14309/crj.0000000000001194 Text en © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Case Report Ramirez Ramirez, Oscar A. Hillman, Luke An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title | An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title_full | An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title_fullStr | An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title_full_unstemmed | An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title_short | An Unusual Disease With a Common Presentation: Cricopharyngeal Dysfunction in Inclusion Body Myositis |
title_sort | unusual disease with a common presentation: cricopharyngeal dysfunction in inclusion body myositis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621890/ https://www.ncbi.nlm.nih.gov/pubmed/37928231 http://dx.doi.org/10.14309/crj.0000000000001194 |
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