Wang Jianwen, Wang Kang, Wu Dengchang, Liang Hui, Zheng Xuning, Luo Benyan
Department of Neurology, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Neurology, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
J Neurol Sci. 2015;353(1-2):81-3. doi: 10.1016/j.jns.2015.04.009. Epub 2015 Apr 15.
Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is a treatable but often misdiagnosed autoimmune encephalitis. Diagnosis depends on NMDAR antibody testing, which may not be readily available. Alternatively, the electroencephalogram (EEG) extreme delta brush pattern may provide a valuable immediate indicator for the diagnosis of anti-NMDAR encephalitis. A 32-year-old female (case 1) presented with fever, headache, behavioral changes, confusion, intractable seizures, central hypoventilation, dysautonomia, facial and limb dyskinesias, and comorbid ovarian teratoma. Cerebral spinal fluid (CSF) testing revealed mild lymphocytic pleocytosis while brain MRI results were normal. A 45-year-old male (case 2) presented with major behavioral changes and rare seizures. Results of routine CSF testing and brain MRI scanning were unremarkable. In both cases, EEG initially revealed the extreme delta brush (EDB) pattern of beta bursting on the peaks and/or the troughs of delta waves, which led to subsequent NMDAR antibody testing and the confirmative diagnosis. Thus, EDB may be a readily accessible sign for suspected anti-NMDAR encephalitis.
抗N-甲基-D-天冬氨酸受体(抗NMDAR)脑炎是一种可治疗但常被误诊的自身免疫性脑炎。诊断依赖于NMDAR抗体检测,而这种检测可能无法随时进行。另外,脑电图(EEG)的极慢波刷状图形可为抗NMDAR脑炎的诊断提供有价值的即时指标。一名32岁女性(病例1)出现发热、头痛、行为改变、意识模糊、难治性癫痫、中枢性通气不足、自主神经功能障碍、面部及肢体运动障碍,并伴有卵巢畸胎瘤。脑脊液(CSF)检测显示轻度淋巴细胞增多,而脑部MRI结果正常。一名45岁男性(病例2)出现主要行为改变及罕见癫痫发作。常规CSF检测和脑部MRI扫描结果均无异常。在这两个病例中,EEG最初均显示在δ波的波峰和/或波谷出现β波爆发的极慢波刷状(EDB)图形,这促使后续进行NMDAR抗体检测并确诊。因此,EDB可能是疑似抗NMDAR脑炎的一个易于获取的体征。