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一例仅抗硫脂抗体阳性相关的眼阵挛:静脉注射免疫球蛋白成功治疗一名儿科患者。

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

作者信息

Akcay Merve, Sager Safiye Günes, Kaplan Aysin Tuba, Alomari Omar, Akin Yasemin

机构信息

Department of Pediatrics, University of Health Sciences, Kartal Dr. Lutfi Kirdar City Hospital, Istanbul, Turkey.

Department of Pediatric Neurology, University of Health Sciences, Kartal Dr. Lutfi Kirdar City Hospital, Istanbul, Turkey.

出版信息

Acta Neurol Belg. 2024 Dec;124(6):2063-2065. doi: 10.1007/s13760-024-02645-3. Epub 2024 Sep 28.

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.

摘要

背景

眼球扑动是一种神经疾病,其特征为不规则、快速的水平眼球运动,常与自身免疫性疾病、感染、药物中毒或副肿瘤综合征相关。参与眼球扑动的脑区尚未明确确定。硫脂是一种酸性糖脂,对维持髓鞘完整性和神经元传递至关重要。抗硫脂抗体可破坏神经元信号,其形成与格林-巴利综合征和GALOP综合征等自身免疫性疾病有关。据我们所知,尚无与硫脂抗体阳性神经病相关的小儿眼球扑动病例报道。

病例描述

一名15岁男性,无病史,出现视振荡和视力模糊。他的产前、出生时及发育史均无异常。神经系统检查发现快速、低幅度的水平扫视振荡(眼球扑动),无其他神经系统异常。广泛检查,包括脑部和脊柱的MRI、血液检查、腰椎穿刺以及病毒、细菌和自身免疫性疾病筛查,结果均正常或为阴性。检测到高滴度的抗硫脂IgM抗体。患者接受静脉注射免疫球蛋白(IVIG)治疗,眼球扑动完全消失。在3个月的随访中,他的神经系统检查正常,每月接受IVIG输注,仍无症状。

结论

这是首例仅与抗硫脂抗体阳性相关的眼球扑动报道病例。这一发现强调了在非典型或治疗抵抗性眼球扑动病例中考虑硫脂抗体检测的重要性。IVIG治疗后症状缓解表明其在治疗硫脂抗体阳性疾病方面的潜在有效性。需要进一步研究以探讨硫脂抗体在眼球扑动中的作用以及靶向免疫治疗的益处。

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