Department of Neurology, Sir Ganga Ram Hospital, Old Rajendra Nagar, New Delhi, India.
Neurol India. 2021 Mar-Apr;69(2):493-494. doi: 10.4103/0028-3886.314549.
A 50-year-old male, presented with a two-months history of ascending paresthesias, with continuous twitchings over the body, associated with insomnia. His electromyography (EMG) revealed neuromyotonia and was diagnosed as a case of peripheral nerve hyperexcitability (PNH) syndrome due to Leucin-rich glioma-inactivated 1 (LGI1) antibody. He showed significant improvement with intravenous immunoglobulin and carbamazepine.
一位 50 岁男性，表现为两个月的上升性感觉异常，伴有全身持续性抽搐，伴有失眠。他的肌电图（EMG）显示神经肌强直，被诊断为由于亮氨酸丰富胶质瘤失活 1（LGI1）抗体引起的周围神经兴奋性过高（PNH）综合征。他接受静脉注射免疫球蛋白和卡马西平治疗后有显著改善。
