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伴有抗GQ1b/GT1a抗体阳性的米勒-费希尔综合征与新型冠状病毒肺炎感染相关:一例病例报告

Miller fisher syndrome with positive anti-GQ1b/GT1a antibodies associated with COVID-19 infection: A case report.

作者信息

Wei Cheng-Qun, Yu Xuan, Wu Yuan-Yuan, Zhao Qing-Jie

机构信息

Department of Neurology, Huai'an Hospital, Huai'an Cancer Hospital, Huai'an 223001, Jiangsu Province, China.

Department of Neurology, The First Affiliated Hospital of Harbin Medical University, Harbin 150081, Heilongjiang Province, China.

出版信息

World J Clin Cases. 2024 Nov 6;12(31):6500-6505. doi: 10.12998/wjcc.v12.i31.6500.

Abstract

BACKGROUND

Miller fisher syndrome (MFS) is a variant of Guillain-Barré syndrome, an acute immune-mediated peripheral neuropathy that is often secondary to viral infections. Anti-ganglioside antibodies play crucial roles in the development of MFS. The positive rate of ganglioside antibodies is exceptionally high in MFS patients, particularly for anti-GQ1b antibodies. However, the presence of other ganglioside antibodies does not exclude MFS.

CASE SUMMARY

We present a 56-year-old female patient who suddenly developed right blepharoptosis and progressively worsening vision in both eyes. There were flu symptoms prior to onset, and a coronavirus disease 2019 test was positive. On physical examination, the patient exhibited bilateral extraocular muscle paralysis, weakened reflexes in both limbs, and impaired coordination. The cerebrospinal fluid examination results showed no obvious abnormalities. Bilateral peroneal nerve F-waves were not extracted. Serum anti-GD1b IgG and anti-GT1a IgG antibodies were positive. The patient received intravenous methylprednisolone (1000 mg/day), with the dosage gradually decreased. Additionally, intravenous high-dose immunoglobulin treatment was administered for 5 days (0.4 g/kg/day) from day 2 to day 6 of hospitalization. The patient's symptoms improved after treatment with immunoglobulins and hormones.

CONCLUSION

Positive ganglioside antibodies may be used as supporting evidence for the diagnosis; however, the diagnosis of MFS is more reliant on clinical symptoms.

摘要

背景

米勒-费雪综合征(MFS)是吉兰-巴雷综合征的一种变异型,是一种急性免疫介导的周围神经病,常继发于病毒感染。抗神经节苷脂抗体在MFS的发病过程中起关键作用。MFS患者神经节苷脂抗体的阳性率异常高,尤其是抗GQ1b抗体。然而,其他神经节苷脂抗体的存在并不排除MFS。

病例摘要

我们报告一名56岁女性患者,突然出现右眼睑下垂,双眼视力逐渐恶化。发病前有流感症状,新型冠状病毒肺炎检测呈阳性。体格检查时,患者表现为双侧眼球外肌麻痹、双下肢反射减弱及共济失调。脑脊液检查结果无明显异常。双侧腓总神经F波未引出。血清抗GD1b IgG和抗GT1a IgG抗体呈阳性。患者接受静脉注射甲泼尼龙(1000mg/天),剂量逐渐减少。此外,住院第2天至第6天给予静脉注射大剂量免疫球蛋白治疗5天(0.4g/kg/天)。经免疫球蛋白和激素治疗后患者症状改善。

结论

神经节苷脂抗体阳性可作为诊断的支持证据;然而,MFS的诊断更依赖于临床症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7183/11438696/8d3fe780dd50/WJCC-12-6500-g001.jpg

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