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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...

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Autores principales: Labeit, Bendix, Muhle, Paul, Suntrup-Krueger, Sonja, Ahring, Sigrid, Ruck, Tobias, Dziewas, Rainer, Warnecke, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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.
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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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