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Idiopathic unilateral oculomotor nerve palsy: A case report

Cranial nerve III palsy, also known as oculomotor nerve palsy, may result from various causes; however, the etiology remains unknown in some instances. The aim of this case report is to present the authors' experience with two cases of idiopathic cranial nerve III palsy, together with a review...

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Autores principales: Kanazawa, Tokunori, Hino, Utaro, Kuramae, Takumi, Ishihara, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718458/
https://www.ncbi.nlm.nih.gov/pubmed/33305057
http://dx.doi.org/10.1016/j.heliyon.2020.e05651
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author Kanazawa, Tokunori
Hino, Utaro
Kuramae, Takumi
Ishihara, Masayuki
author_facet Kanazawa, Tokunori
Hino, Utaro
Kuramae, Takumi
Ishihara, Masayuki
author_sort Kanazawa, Tokunori
collection PubMed
description Cranial nerve III palsy, also known as oculomotor nerve palsy, may result from various causes; however, the etiology remains unknown in some instances. The aim of this case report is to present the authors' experience with two cases of idiopathic cranial nerve III palsy, together with a review of the literature. Case 1 is a 78-year-old woman and case 2 is a 75-year-old man, both having no history of trauma and no vascular risk factors. They presented to the authors' hospital with diplopia and palpebral ptosis and were diagnosed with idiopathic unilateral cranial nerve III palsy. They received oral steroids for treatment. One patient recovered completely within 3 months, while the other patient did not recover regardless of long-term follow-up. Idiopathic cranial nerve III palsy can occur in otherwise healthy individuals and often recover in several months. Careful examinations to rule out other causes and then steroid treatment should be considered after early diagnosis.
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spelling pubmed-77184582020-12-09 Idiopathic unilateral oculomotor nerve palsy: A case report Kanazawa, Tokunori Hino, Utaro Kuramae, Takumi Ishihara, Masayuki Heliyon Case Report Cranial nerve III palsy, also known as oculomotor nerve palsy, may result from various causes; however, the etiology remains unknown in some instances. The aim of this case report is to present the authors' experience with two cases of idiopathic cranial nerve III palsy, together with a review of the literature. Case 1 is a 78-year-old woman and case 2 is a 75-year-old man, both having no history of trauma and no vascular risk factors. They presented to the authors' hospital with diplopia and palpebral ptosis and were diagnosed with idiopathic unilateral cranial nerve III palsy. They received oral steroids for treatment. One patient recovered completely within 3 months, while the other patient did not recover regardless of long-term follow-up. Idiopathic cranial nerve III palsy can occur in otherwise healthy individuals and often recover in several months. Careful examinations to rule out other causes and then steroid treatment should be considered after early diagnosis. Elsevier 2020-12-03 /pmc/articles/PMC7718458/ /pubmed/33305057 http://dx.doi.org/10.1016/j.heliyon.2020.e05651 Text en © 2020 The Author(s) 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
Kanazawa, Tokunori
Hino, Utaro
Kuramae, Takumi
Ishihara, Masayuki
Idiopathic unilateral oculomotor nerve palsy: A case report
title Idiopathic unilateral oculomotor nerve palsy: A case report
title_full Idiopathic unilateral oculomotor nerve palsy: A case report
title_fullStr Idiopathic unilateral oculomotor nerve palsy: A case report
title_full_unstemmed Idiopathic unilateral oculomotor nerve palsy: A case report
title_short Idiopathic unilateral oculomotor nerve palsy: A case report
title_sort idiopathic unilateral oculomotor nerve palsy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718458/
https://www.ncbi.nlm.nih.gov/pubmed/33305057
http://dx.doi.org/10.1016/j.heliyon.2020.e05651
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