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Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a condition that mainly affects the peripheral nervous system; however, the central nervous system has also been involved in rare cases. Herein, we describe the case of a 33-year-old man with CIDP who presented with progressively blurred vi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602723/ https://www.ncbi.nlm.nih.gov/pubmed/29018664 http://dx.doi.org/10.1016/j.tjo.2014.04.002 |
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author | Lin, Kui-Yueh Wang, I-Hua Jou, Jieh-Ren Chu, Hai-Jui Wei, William Lee, Shwu-Huey Lin, Szu-Yuan |
author_facet | Lin, Kui-Yueh Wang, I-Hua Jou, Jieh-Ren Chu, Hai-Jui Wei, William Lee, Shwu-Huey Lin, Szu-Yuan |
author_sort | Lin, Kui-Yueh |
collection | PubMed |
description | Chronic inflammatory demyelinating polyneuropathy (CIDP) is a condition that mainly affects the peripheral nervous system; however, the central nervous system has also been involved in rare cases. Herein, we describe the case of a 33-year-old man with CIDP who presented with progressively blurred vision and pain with eye movement in both eyes for 1 month. Ocular examination revealed reduced visual acuities of 0.15 (oculus unitas or OU) and unremarkable fundi (OU). Furthermore, bitemporal visual field defects and prolonged visually evoked potentials were evident. Brain magnetic resonance imaging revealed nothing remarkable along the optic nerve and chiasm. These findings were compatible with the diagnosis of bilateral optic neuritis. The patient's symptoms and visual acuity improved after 5 days of intravenous (IV) corticosteroid pulse therapy, which was subsequently replaced by oral prednisolone therapy with a tapering schedule. The patient's visual acuity returned to 1.0 (OU) 6 months after treatment. However, bilateral optic neuritis recurred in 7 months while the patient was on oral prednisolone and azathioprine. IV corticosteroid pulse therapy was subsequently reinitiated and the patient's visual acuity returned gradually to 1.0 (OU). Bilateral optic neuritis is a rare manifestation of CIDP. It responded well to IV corticosteroid therapy in our case. |
format | Online Article Text |
id | pubmed-5602723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56027232017-10-10 Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy Lin, Kui-Yueh Wang, I-Hua Jou, Jieh-Ren Chu, Hai-Jui Wei, William Lee, Shwu-Huey Lin, Szu-Yuan Taiwan J Ophthalmol Case Report Chronic inflammatory demyelinating polyneuropathy (CIDP) is a condition that mainly affects the peripheral nervous system; however, the central nervous system has also been involved in rare cases. Herein, we describe the case of a 33-year-old man with CIDP who presented with progressively blurred vision and pain with eye movement in both eyes for 1 month. Ocular examination revealed reduced visual acuities of 0.15 (oculus unitas or OU) and unremarkable fundi (OU). Furthermore, bitemporal visual field defects and prolonged visually evoked potentials were evident. Brain magnetic resonance imaging revealed nothing remarkable along the optic nerve and chiasm. These findings were compatible with the diagnosis of bilateral optic neuritis. The patient's symptoms and visual acuity improved after 5 days of intravenous (IV) corticosteroid pulse therapy, which was subsequently replaced by oral prednisolone therapy with a tapering schedule. The patient's visual acuity returned to 1.0 (OU) 6 months after treatment. However, bilateral optic neuritis recurred in 7 months while the patient was on oral prednisolone and azathioprine. IV corticosteroid pulse therapy was subsequently reinitiated and the patient's visual acuity returned gradually to 1.0 (OU). Bilateral optic neuritis is a rare manifestation of CIDP. It responded well to IV corticosteroid therapy in our case. Medknow Publications & Media Pvt Ltd 2015 2014-06-23 /pmc/articles/PMC5602723/ /pubmed/29018664 http://dx.doi.org/10.1016/j.tjo.2014.04.002 Text en Copyright: © 2014, The Ophthalmologic Society of Taiwan http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Lin, Kui-Yueh Wang, I-Hua Jou, Jieh-Ren Chu, Hai-Jui Wei, William Lee, Shwu-Huey Lin, Szu-Yuan Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title | Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title_full | Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title_fullStr | Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title_full_unstemmed | Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title_short | Bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
title_sort | bilateral optic neuritis related to chronic inflammatory demyelinating polyneuropathy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602723/ https://www.ncbi.nlm.nih.gov/pubmed/29018664 http://dx.doi.org/10.1016/j.tjo.2014.04.002 |
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