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

被引：0

作者：

Park, Soo-Hyun ^{[1
]}

Jang, Soo-Im ^{[2
]}

Lee, Eun-Ja ^{[3
]}

Kim, Nam-Hee ^{[2
]}

机构：

[1] Soon Chunhyang Univ, Dept Neurol, Seoul, South Korea

[2] Dongguk Univ, Ilsan Hosp, Dept Neurol, Goyang, South Korea

[3] Dongguk Univ, Ilsan Hosp, Dept Radiol, Goyang, South Korea

来源：

FRONTIERS IN NEUROLOGY | 2024年 / 15卷

关键词：

optic neuritis; neuromyelitis optica spectrum disorder; Tolosa-Hunt syndrome; abducens palsy; aquaporin-4; antibody; AQP4-immunoglobulin G; DIAGNOSTIC-CRITERIA;

D O I：

10.3389/fneur.2024.1326867

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

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.

引用

页数：4

共 17 条

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