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Case report: Tolosa-Hunt syndrome—expanding the neuromyelitis optica spectrum disorder phenotype?open access

Authors
Park, Soo-HyunJang, Soo-ImLee, Eun-JaKim, 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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