Cui Junzhao, Bu Hui, He Junying, Zhao Zeyan, Han Weixin, Gao Ruiping, Li Xiaoqing, Li Qing, Guo Xiaosu, Zou Yueli
a Department of Neurology , Second Hospital of Hebei Medical University , Shijiazhuang , China.
Int J Neurosci. 2018 Jul;128(7):627-633. doi: 10.1080/00207454.2017.1408618. Epub 2017 Dec 6.
We report 11 patients diagnosed with GABAB receptor (GABABR) antibodies encephalitis in China and aim to analyze the clinical characteristics, laboratory and imaging findings, therapeutic modalities and outcomes.
Clinical data from patients diagnosed with anti-GABAB receptor encephalitis in the Second Affiliated Hospital of Hebei Medical University from February 2016 to October 2016 January were retrospectively collected and evaluated.
Of the 11 patients, seven were males, and a mean age at presentation of 63 years (range: 47-79 years). The major clinical features include cognitive decline (9/11), epilepsy (10/11), mental and behavioral disorders (6/11), involuntary movement (4/11), sleep disorders (2/11), hearing loss (1/11), disturbance of consciousness (4/11) and fever (3/11). GABA-B receptor antibody was positive in serum and/or cerebrospinal fluid in 11 patients. Small-cell lung cancer was detected in five patients. Electroencephalogram monitoring demonstrated abnormal discharge in 10 cases. Epileptiform activities were found in five patients. Four patients showed abnormality in hippocampal region, parahippocampal gyrus, temporal and occipital lobe on magnetic resonance imaging. Ten patients accepted first-line immune therapy. Five patients with small-cell lung cancer received oncologic treatment. During a median follow-up of 11 months, eight patients showed a good outcome, two patients (cases 8 and 9) with tumors had a poor one and one patient (case 10) died of status epilepticus.
Anti-GABAB receptor encephalitis is an uncommon autoimmune disease, which has been known to be often associated with cancer. Generally, patients associated with GABABR GABA-B receptor antibody encephalitis respond well to immunotherapy, especially if started early.
我们报告了11例在中国被诊断为GABAB受体(GABABR)抗体脑炎的患者,并旨在分析其临床特征、实验室及影像学检查结果、治疗方式及预后。
回顾性收集并评估2016年2月至2016年10月在河北医科大学第二附属医院被诊断为抗GABAB受体脑炎患者的临床资料。
11例患者中,7例为男性,就诊时平均年龄63岁(范围:47 - 79岁)。主要临床特征包括认知功能下降(9/11)、癫痫(10/11)、精神和行为障碍(6/11)、不自主运动(4/11)、睡眠障碍(2/11)、听力丧失(1/11)、意识障碍(4/11)和发热(3/11)。11例患者血清和/或脑脊液中GABA - B受体抗体呈阳性。5例患者检测出小细胞肺癌。脑电图监测显示10例异常放电。5例患者发现癫痫样活动。4例患者磁共振成像显示海马区、海马旁回、颞叶和枕叶异常。10例患者接受一线免疫治疗。5例小细胞肺癌患者接受肿瘤治疗。中位随访11个月期间,8例患者预后良好,2例(病例8和9)有肿瘤的患者预后较差,1例患者(病例10)死于癫痫持续状态。
抗GABAB受体脑炎是一种罕见的自身免疫性疾病,已知常与癌症相关。一般来说,与GABABR GABA - B受体抗体脑炎相关的患者对免疫治疗反应良好,尤其是早期开始治疗时。