Case report: Tolosa-Hunt syndrome—expanding the neuromyelitis optica spectrum disorder phenotype?open access
- Authors
- Park, Soo-Hyun; Jang, Soo-Im; Lee, Eun-Ja; Kim, Nam-Hee
- Issue Date
- Feb-2024
- Publisher
- Frontiers Media SA
- Keywords
- abducens palsy; AQP4-immunoglobulin G; aquaporin-4 antibody; neuromyelitis optica spectrum disorder; optic neuritis; Tolosa-Hunt syndrome
- Citation
- Frontiers in Neurology, v.15, pp 01 - 04
- Pages
- 4
- Indexed
- SCIE
SCOPUS
- Journal Title
- Frontiers in Neurology
- Volume
- 15
- Start Page
- 01
- End Page
- 04
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/22783
- DOI
- 10.3389/fneur.2024.1326867
- ISSN
- 1664-2295
1664-2295
- Abstract
- Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune astrocytopathy caused by the autoantibody of aquaporin-4 (AQP4). Herein, we report a case of Tolosa-Hunt syndrome presenting with abducens palsy and AQP4 antibodies. This was a rare case of AQP4-immunoglobulin G seropositivity in a patient with Tolosa-Hunt syndrome. Our findings may expand the clinical phenotype of NMOSD and indicate that clinicians should consider testing for AQP4 antibodies in patients with Tolosa-Hunt syndrome. Copyright © 2024 Park, Jang, Lee and Kim.
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Collections - Graduate School > Department of Medicine > 1. Journal Articles

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