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Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis?
Dysphagia can be predominant or sole symptom of myositis. However, diagnostic evaluation is difficult in such cases. Here, we present evidence for dysphagia as sole manifestation of Jo-1 associated myositis. A 77-year-old patient suffering from isolated dysphagia was assessed by flexible endoscopic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629889/ https://www.ncbi.nlm.nih.gov/pubmed/31338062 http://dx.doi.org/10.3389/fneur.2019.00739 |
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author | Labeit, Bendix Muhle, Paul Suntrup-Krueger, Sonja Ahring, Sigrid Ruck, Tobias Dziewas, Rainer Warnecke, Tobias |
author_facet | Labeit, Bendix Muhle, Paul Suntrup-Krueger, Sonja Ahring, Sigrid Ruck, Tobias Dziewas, Rainer Warnecke, Tobias |
author_sort | Labeit, Bendix |
collection | PubMed |
description | Dysphagia can be predominant or sole symptom of myositis. However, diagnostic evaluation is difficult in such cases. Here, we present evidence for dysphagia as sole manifestation of Jo-1 associated myositis. A 77-year-old patient suffering from isolated dysphagia was assessed by flexible endoscopic evaluation of swallowing, videofluoroscopy, high resolution esophageal manometry, whole body muscle MRI, electroneurographic and electromyographic examination, cerebrospinal fluid analysis, screening for autoantibodies, and body plethysmography. We detected isolated oropharyngeal dysphagia including a decreased pressure of the upper esophageal sphincter leading to cachexia in an anti-Jo-1 positive patient without any abnormalities in the other diagnostics. Immunosuppressive therapy with cortisone and azathioprine led to long-term improvement of dysphagia. This is the first report of isolated dysphagia as manifestation of Jo-1 associated myositis. Therefore, Jo-1 associated myositis should be considered as a possible differential diagnosis for isolated dysphagia. Typical signs for myositis in instrumental dysphagia assessment are presented. |
format | Online Article Text |
id | pubmed-6629889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66298892019-07-23 Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? Labeit, Bendix Muhle, Paul Suntrup-Krueger, Sonja Ahring, Sigrid Ruck, Tobias Dziewas, Rainer Warnecke, Tobias Front Neurol Neurology Dysphagia can be predominant or sole symptom of myositis. However, diagnostic evaluation is difficult in such cases. Here, we present evidence for dysphagia as sole manifestation of Jo-1 associated myositis. A 77-year-old patient suffering from isolated dysphagia was assessed by flexible endoscopic evaluation of swallowing, videofluoroscopy, high resolution esophageal manometry, whole body muscle MRI, electroneurographic and electromyographic examination, cerebrospinal fluid analysis, screening for autoantibodies, and body plethysmography. We detected isolated oropharyngeal dysphagia including a decreased pressure of the upper esophageal sphincter leading to cachexia in an anti-Jo-1 positive patient without any abnormalities in the other diagnostics. Immunosuppressive therapy with cortisone and azathioprine led to long-term improvement of dysphagia. This is the first report of isolated dysphagia as manifestation of Jo-1 associated myositis. Therefore, Jo-1 associated myositis should be considered as a possible differential diagnosis for isolated dysphagia. Typical signs for myositis in instrumental dysphagia assessment are presented. Frontiers Media S.A. 2019-07-09 /pmc/articles/PMC6629889/ /pubmed/31338062 http://dx.doi.org/10.3389/fneur.2019.00739 Text en Copyright © 2019 Labeit, Muhle, Suntrup-Krueger, Ahring, Ruck, Dziewas and Warnecke. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Labeit, Bendix Muhle, Paul Suntrup-Krueger, Sonja Ahring, Sigrid Ruck, Tobias Dziewas, Rainer Warnecke, Tobias Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title | Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title_full | Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title_fullStr | Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title_full_unstemmed | Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title_short | Dysphagia as Isolated Manifestation of Jo-1 Associated Myositis? |
title_sort | dysphagia as isolated manifestation of jo-1 associated myositis? |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629889/ https://www.ncbi.nlm.nih.gov/pubmed/31338062 http://dx.doi.org/10.3389/fneur.2019.00739 |
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