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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
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.
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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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