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A case of oculomotor nerve palsy associated with antimitotic spindle apparatus
In this case report, we describe a case of isolated oculomotor nerve palsy associated with antibodies to mitotic spindle apparatus (anti-MSA). A 28-year-old female patient had acute, painful vertical diplopia. She had limited depression and adduction in the right eye. There was no relative afferent...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096615/ https://www.ncbi.nlm.nih.gov/pubmed/21607022 http://dx.doi.org/10.2147/OPTH.S16864 |
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author | Jung, Jong Jin Kim, Ungsoo Samuel |
author_facet | Jung, Jong Jin Kim, Ungsoo Samuel |
author_sort | Jung, Jong Jin |
collection | PubMed |
description | In this case report, we describe a case of isolated oculomotor nerve palsy associated with antibodies to mitotic spindle apparatus (anti-MSA). A 28-year-old female patient had acute, painful vertical diplopia. She had limited depression and adduction in the right eye. There was no relative afferent pupillary defect. Brain magnetic resonance imaging showed no abnormal findings. Laboratory tests were all negative, with the exception of positive anti-MSA, She had an excellent and rapid response to treatment with corticosteroids, and completely recovered after two weeks of steroid pulse therapy. |
format | Text |
id | pubmed-3096615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30966152011-05-23 A case of oculomotor nerve palsy associated with antimitotic spindle apparatus Jung, Jong Jin Kim, Ungsoo Samuel Clin Ophthalmol Case Report In this case report, we describe a case of isolated oculomotor nerve palsy associated with antibodies to mitotic spindle apparatus (anti-MSA). A 28-year-old female patient had acute, painful vertical diplopia. She had limited depression and adduction in the right eye. There was no relative afferent pupillary defect. Brain magnetic resonance imaging showed no abnormal findings. Laboratory tests were all negative, with the exception of positive anti-MSA, She had an excellent and rapid response to treatment with corticosteroids, and completely recovered after two weeks of steroid pulse therapy. Dove Medical Press 2011 2011-04-28 /pmc/articles/PMC3096615/ /pubmed/21607022 http://dx.doi.org/10.2147/OPTH.S16864 Text en © 2011 Jung and Kim, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Case Report Jung, Jong Jin Kim, Ungsoo Samuel A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title | A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title_full | A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title_fullStr | A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title_full_unstemmed | A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title_short | A case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
title_sort | case of oculomotor nerve palsy associated with antimitotic spindle apparatus |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096615/ https://www.ncbi.nlm.nih.gov/pubmed/21607022 http://dx.doi.org/10.2147/OPTH.S16864 |
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