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Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis
Here, we describe a 79-year-old man, admitted to our unit for worsening diplopia and fatigue, started a few weeks after an episode of bronchitis and flu vaccination. Past medical history includes myasthenia gravis (MG), well-controlled by Pyridostigmine, Azathioprine, and Prednisone. During the firs...
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/PMC6700242/ https://www.ncbi.nlm.nih.gov/pubmed/31456730 http://dx.doi.org/10.3389/fneur.2019.00823 |
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author | Brusa, Roberta Faravelli, Irene Gagliardi, Delia Magri, Francesca Cogiamanian, Filippo Saccomanno, Domenica Cinnante, Claudia Mauri, Eleonora Abati, Elena Bresolin, Nereo Corti, Stefania Comi, Giacomo Pietro |
author_facet | Brusa, Roberta Faravelli, Irene Gagliardi, Delia Magri, Francesca Cogiamanian, Filippo Saccomanno, Domenica Cinnante, Claudia Mauri, Eleonora Abati, Elena Bresolin, Nereo Corti, Stefania Comi, Giacomo Pietro |
author_sort | Brusa, Roberta |
collection | PubMed |
description | Here, we describe a 79-year-old man, admitted to our unit for worsening diplopia and fatigue, started a few weeks after an episode of bronchitis and flu vaccination. Past medical history includes myasthenia gravis (MG), well-controlled by Pyridostigmine, Azathioprine, and Prednisone. During the first days, the patient developed progressive ocular movement abnormalities up to complete external ophthalmoplegia, severe limb and gait ataxia, and mild dysarthria. Deep tendon reflexes were absent in lower limbs. Since not all the symptoms were explainable with the previous diagnosis of myasthenia gravis, other etiologies were investigated. Brain MRI and cerebrospinal fluid analysis were normal. Electromyography showed a pattern of predominantly sensory multiple radiculoneuritis. Suspecting Miller Fisher syndrome (MFS), the patient was treated with plasmapheresis with subsequent clinical improvement. Antibodies against GQ1b turned out to be positive. MFS is an immune-mediated neuropathy presenting with ophthalmoplegia, ataxia, and areflexia. Even if only a few cases of MFS overlapping with MG have been described so far, the coexistence of two different autoimmune disorders can occur. It is always important to evaluate possible differential diagnosis even in case of known compatible diseases, especially when some clinical features seem atypical. |
format | Online Article Text |
id | pubmed-6700242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67002422019-08-27 Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis Brusa, Roberta Faravelli, Irene Gagliardi, Delia Magri, Francesca Cogiamanian, Filippo Saccomanno, Domenica Cinnante, Claudia Mauri, Eleonora Abati, Elena Bresolin, Nereo Corti, Stefania Comi, Giacomo Pietro Front Neurol Neurology Here, we describe a 79-year-old man, admitted to our unit for worsening diplopia and fatigue, started a few weeks after an episode of bronchitis and flu vaccination. Past medical history includes myasthenia gravis (MG), well-controlled by Pyridostigmine, Azathioprine, and Prednisone. During the first days, the patient developed progressive ocular movement abnormalities up to complete external ophthalmoplegia, severe limb and gait ataxia, and mild dysarthria. Deep tendon reflexes were absent in lower limbs. Since not all the symptoms were explainable with the previous diagnosis of myasthenia gravis, other etiologies were investigated. Brain MRI and cerebrospinal fluid analysis were normal. Electromyography showed a pattern of predominantly sensory multiple radiculoneuritis. Suspecting Miller Fisher syndrome (MFS), the patient was treated with plasmapheresis with subsequent clinical improvement. Antibodies against GQ1b turned out to be positive. MFS is an immune-mediated neuropathy presenting with ophthalmoplegia, ataxia, and areflexia. Even if only a few cases of MFS overlapping with MG have been described so far, the coexistence of two different autoimmune disorders can occur. It is always important to evaluate possible differential diagnosis even in case of known compatible diseases, especially when some clinical features seem atypical. Frontiers Media S.A. 2019-08-13 /pmc/articles/PMC6700242/ /pubmed/31456730 http://dx.doi.org/10.3389/fneur.2019.00823 Text en Copyright © 2019 Brusa, Faravelli, Gagliardi, Magri, Cogiamanian, Saccomanno, Cinnante, Mauri, Abati, Bresolin, Corti and Comi. 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 Brusa, Roberta Faravelli, Irene Gagliardi, Delia Magri, Francesca Cogiamanian, Filippo Saccomanno, Domenica Cinnante, Claudia Mauri, Eleonora Abati, Elena Bresolin, Nereo Corti, Stefania Comi, Giacomo Pietro Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title | Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title_full | Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title_fullStr | Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title_full_unstemmed | Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title_short | Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis |
title_sort | ophthalmoplegia due to miller fisher syndrome in a patient with myasthenia gravis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6700242/ https://www.ncbi.nlm.nih.gov/pubmed/31456730 http://dx.doi.org/10.3389/fneur.2019.00823 |
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