Optic neuritis associated with seronegative autoimmune encephalitis: a case report.

Hyungseok Hah, Yonghyun Lee, Ho-Won Lee, Ji-Ye Jeon
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Abstract

Optic neuritis is an inflammatory demyelinating disorder that primarily affects the optic nerve and is often associated with multiple sclerosis. While it is rare for optic neuritis to be accompanied by autoimmune encephalitis, it can occur in some cases. A 65-year-old woman with bipolar disorder presented with a progressively altered mentality. Magnetic resonance imaging of the brain showed no definite abnormal findings. Electroencephalography revealed nonconvulsive status epilepticus. Cerebrospinal fluid study and autoimmune and paraneoplastic encephalitis antibodies were negative. The patient was diagnosed with seronegative autoimmune encephalitis and treated with methylprednisolone, intravenous immunoglobulin, and rituximab. Her condition gradually improved except for persistent blindness on the left side. This case highlights the importance of considering autoimmune encephalitis even in the absence of identifiable pathogenic antibodies when clinical manifestations and response to immunotherapy support such a diagnosis.

Abstract Image

视神经炎合并血清阴性自身免疫性脑炎1例
视神经炎是一种炎性脱髓鞘疾病,主要影响视神经,通常与多发性硬化症有关。虽然视神经炎很少伴有自身免疫性脑炎,但在某些情况下也会发生。65岁女性双相情感障碍表现为逐渐改变的心态。脑磁共振成像未见明显异常。脑电图显示非惊厥性癫痫持续状态。脑脊液检查、自身免疫和副肿瘤脑炎抗体均为阴性。患者被诊断为血清阴性自身免疫性脑炎,并接受甲基强的松龙、静脉注射免疫球蛋白和利妥昔单抗治疗。除了左侧持续失明外,她的病情逐渐好转。本病例强调了考虑自身免疫性脑炎的重要性,即使在没有可识别的致病抗体时,当临床表现和对免疫治疗的反应支持这种诊断。
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