A case of ocular flutter associated with sole anti-sulphatide antibody positivity: successful treatment with intravenous immunoglobulin in a pediatric patient.

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY Acta neurologica Belgica Pub Date : 2024-09-28 DOI:10.1007/s13760-024-02645-3
Merve Akcay, Safiye Günes Sager, Aysin Tuba Kaplan, Omar Alomari, Yasemin Akin
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Abstract

Background: Ocular flutter is a neurological disorder characterized by irregular, rapid horizontal eye movements and is often associated with autoimmune diseases, infections, drug intoxication, or paraneoplastic syndromes. The brain regions involved in ocular flutter have not been definitively determined. Sulfatide is an acidic glycolipid crucial for maintaining myelin sheath integrity and neuronal transmission. Antibodies against sulfatide can disrupt neuronal signals, and their formation is linked to autoimmune conditions such as Guillain-Barré syndrome and GALOP syndrome. To our knowledge, no pediatric cases of ocular flutter associated with sulfatide antibody-positive neuropathy have been reported.

Case description: A 15-year-old male with no medical history presented with oscillopsia and blurred vision. His prenatal, natal, and developmental history were unremarkable. Neurological examination revealed rapid, low-amplitude horizontal saccadic oscillations (ocular flutter) with no other neurological abnormalities. Extensive testing, including MRI of the brain and spine; blood tests; lumbar puncture; and screenings for viral, bacterial, and autoimmune conditions, returned normal or negative results. A high titer of anti-sulfatide IgM antibodies was detected. The patient was treated with intravenous immunoglobulin (IVIG), which led to complete resolution of ocular flutter. At the 3-month follow-up, his neurological examination was normal, and he remained asymptomatic with monthly IVIG infusions.

Conclusion: This is the first reported case of ocular flutter associated solely with anti-sulfatide antibody positivity. This finding underscores the importance of considering sulfatide antibody testing in atypical or treatment-resistant cases of ocular flutter. The resolution of symptoms following IVIG treatment suggests its potential effectiveness in managing sulfatide antibody-positive conditions. Further research is needed to explore the role of sulfatide antibodies in ocular flutter and the benefits of targeted immunotherapy.

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一例伴有唯一抗硫肽抗体阳性的眼扑病例:一名儿童患者通过静脉注射免疫球蛋白获得成功治疗。
背景:眼跳是一种以不规则、快速的水平眼球运动为特征的神经系统疾病,通常与自身免疫性疾病、感染、药物中毒或副肿瘤综合征有关。眼球震颤所涉及的脑区尚未明确确定。硫甙是一种酸性糖脂,对维持髓鞘完整性和神经元传导至关重要。针对硫甙的抗体会破坏神经元信号,其形成与吉兰-巴雷综合征和 GALOP 综合征等自身免疫性疾病有关。据我们所知,还没有与磺胺抗体阳性神经病变相关的眼扑儿科病例报道:病例描述:一名 15 岁的男性患者,无病史,出现眼球震荡和视力模糊。他的产前、出生和发育史均无异常。神经系统检查显示,他有快速、低振幅的水平囊状摆动(眼球跳动),没有其他神经系统异常。广泛的检查,包括脑部和脊柱的核磁共振成像、血液检测、腰椎穿刺以及病毒、细菌和自身免疫疾病筛查,结果均为正常或阴性。检测出抗硫化物 IgM 抗体滴度较高。患者接受了静脉注射免疫球蛋白(IVIG)治疗,结果眼扑症状完全缓解。在 3 个月的随访中,他的神经系统检查正常,每月输注 IVIG 仍无症状:结论:这是首例仅与抗硫酸抗体阳性相关的眼扑病例。这一发现强调了在非典型或治疗耐药的眼扑病例中考虑进行硫酰胺抗体检测的重要性。IVIG 治疗后症状的缓解表明,它在治疗硫肽酶抗体阳性病症方面具有潜在的疗效。还需要进一步研究硫肽抗体在眼扑中的作用以及靶向免疫疗法的益处。
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来源期刊
Acta neurologica Belgica
Acta neurologica Belgica 医学-临床神经学
CiteScore
4.20
自引率
3.70%
发文量
300
审稿时长
6-12 weeks
期刊介绍: Peer-reviewed and published quarterly, Acta Neurologica Belgicapresents original articles in the clinical and basic neurosciences, and also reports the proceedings and the abstracts of the scientific meetings of the different partner societies. The contents include commentaries, editorials, review articles, case reports, neuro-images of interest, book reviews and letters to the editor. Acta Neurologica Belgica is the official journal of the following national societies: Belgian Neurological Society Belgian Society for Neuroscience Belgian Society of Clinical Neurophysiology Belgian Pediatric Neurology Society Belgian Study Group of Multiple Sclerosis Belgian Stroke Council Belgian Headache Society Belgian Study Group of Neuropathology
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