Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology, Baylor College of Medicine, Houston, TX, USA; University of Guanajuato, Mexico.
National Polytechnic Institute, Mexico.
J Neuroimmunol. 2018 Apr 15;317:5-7. doi: 10.1016/j.jneuroim.2018.01.013. Epub 2018 Feb 3.
Several neurological disorders have been described in patients with autoimmunity associated with GAD antibodies. Among these disorders, nystagmus and oculomotor dysfunction are increasingly recognized, although they have been rarely reported isolated or as the main manifestation of anti-GAD autoimmunity. Moreover, therapeutic approaches for such patients are unclear. Here we present a 44-year-old man with disabling oscillopsia secondary to downbeat nystagmus, abnormal saccades, ocular pursuit and optokinetic nystagmus, as well as mild gait ataxia and cerebellar atrophy associated with high serum GAD antibodies with intrathecal secretion of such antibodies. The patient did not have clinical benefit with plasma exchange, but had a robust symptomatic improvement with cyclophosphamide. We discuss the possible pathogenic role of GAD antibodies in nystagmus and the role of immunotherapy in these patients.
已在伴发 GAD 抗体的自身免疫患者中描述了几种神经紊乱。在这些紊乱中,眼球震颤和眼动功能障碍越来越受到关注,尽管它们很少被孤立报道或作为抗 GAD 自身免疫的主要表现。此外,此类患者的治疗方法尚不清楚。在此,我们介绍了一名 44 岁男性患者,因低位性眼球震颤继发的致残性眼球震颤、异常扫视、眼球追踪和视动性眼球震颤、以及轻度步态共济失调和小脑萎缩而就诊,其血清 GAD 抗体滴度高,且存在此类抗体的鞘内分泌。该患者行血浆置换治疗后无临床获益,但使用环磷酰胺后症状明显改善。我们讨论了 GAD 抗体在眼球震颤中的可能致病作用,以及免疫治疗在这些患者中的作用。