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An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission

A male patient developed ocular myasthenia gravis (MG) at the age of 33. He was anti-acetylcholine receptor antibody (anti-AChR Ab) negative. He received cholinesterase blocker for 5 months and went into a complete clinical remission that lasted untreated for 17 years. He relapsed recently with ocul...

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Autores principales: Al-Hashel, Jasem, Rashad, Hanaa M., Rousseff, Rossen T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005048/
https://www.ncbi.nlm.nih.gov/pubmed/24822137
http://dx.doi.org/10.1155/2014/372769
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author Al-Hashel, Jasem
Rashad, Hanaa M.
Rousseff, Rossen T.
author_facet Al-Hashel, Jasem
Rashad, Hanaa M.
Rousseff, Rossen T.
author_sort Al-Hashel, Jasem
collection PubMed
description A male patient developed ocular myasthenia gravis (MG) at the age of 33. He was anti-acetylcholine receptor antibody (anti-AChR Ab) negative. He received cholinesterase blocker for 5 months and went into a complete clinical remission that lasted untreated for 17 years. He relapsed recently with ocular symptoms only. He is now anti-AChR Ab positive and SFEMG is abnormal in a facial muscle. The patient is controlled with steroids. He had one of the longest spontaneous remissions reported in the natural history of MG, particularly unusual for an adult with the disease.
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spelling pubmed-40050482014-05-12 An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission Al-Hashel, Jasem Rashad, Hanaa M. Rousseff, Rossen T. Case Rep Neurol Med Case Report A male patient developed ocular myasthenia gravis (MG) at the age of 33. He was anti-acetylcholine receptor antibody (anti-AChR Ab) negative. He received cholinesterase blocker for 5 months and went into a complete clinical remission that lasted untreated for 17 years. He relapsed recently with ocular symptoms only. He is now anti-AChR Ab positive and SFEMG is abnormal in a facial muscle. The patient is controlled with steroids. He had one of the longest spontaneous remissions reported in the natural history of MG, particularly unusual for an adult with the disease. Hindawi Publishing Corporation 2014 2014-04-13 /pmc/articles/PMC4005048/ /pubmed/24822137 http://dx.doi.org/10.1155/2014/372769 Text en Copyright © 2014 Jasem Al-Hashel et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Hashel, Jasem
Rashad, Hanaa M.
Rousseff, Rossen T.
An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title_full An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title_fullStr An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title_full_unstemmed An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title_short An Adult Patient with Ocular Myasthenia and Unusually Long Spontaneous Remission
title_sort adult patient with ocular myasthenia and unusually long spontaneous remission
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005048/
https://www.ncbi.nlm.nih.gov/pubmed/24822137
http://dx.doi.org/10.1155/2014/372769
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