Guan Hong-Zhi, Ren Hai-Tao, Yang Xun-Zhe, Lu Qiang, Peng Bin, Zhu Yi-Cheng, Shao Xiao-Qiu, Hu Yong-Qiang, Zhou Dong, Cui Li-Ying
Department of Neurology, Peking Union Medical College Hospital; Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Chin Med J (Engl). 2015 Nov 20;128(22):3023-8. doi: 10.4103/0366-6999.168989.
Autoimmune encephalitis associated with antibodies against γ-aminobutyric acid B receptor (GABA B R) in patients with limbic encephalitis (LE) was first described in 2010. We present a series of Han Chinese patients for further clinical refinement.
Serum and cerebrospinal fluid (CSF) samples from patients referred to the program of encephalitis and paraneoplastic syndrome of Peking Union Medical College Hospital were tested with indirect immunofluorescence. Clinical information of patients with anti-GABA B R antibody positivity was retrospectively reviewed, and descriptive statistical analysis was performed.
All eighteen anti-GABA B R antibody-positive cases had limbic syndromes, and electroencephalogram (EEG) or neuroimaging evidence fulfilled the diagnostic criteria of LE. Four patients had additional antibodies against Hu in serum and one had anti-N-methyl-d-aspartate receptor antibody in both sera and CSF. Seventeen (17/18) patients presented with new-onset refractory seizure or status epileptics. Twelve (12/18) patients had memory deficits, 11 (11/18) patients had personality change, 7 (7/18) patients had disturbance of consciousness, and 3 (3/18) patients showed cerebellar dysfunction. One patient with LE had progressive motor and sensory polyneuropathy. Lung cancer was detected in 6 (6/18) patients. Ten (10/18) patients showed abnormality in bilateral or unilateral mediotemporal region on magnetic resonance imaging. Ten (10/18) patients had temporal lobe epileptic activity with or without general slowing on EEG. Seventeen patients received immunotherapy and 15 of them showed neurological improvement. Four patients with lung cancer died within 1-12 months due to neoplastic complications.
Our study demonstrates that most Han Chinese patients with anti-GABA B R antibody-associated LE have prominent refractory epilepsy and show neurological improvement on immunotherapy. Patients with underlying lung tumor have a relatively poor prognosis. Testing for anti-GABA B R antibodies is necessary for patients with possible LE or new-onset epilepsy with unknown etiology.
2010年首次报道了与抗γ-氨基丁酸B受体(GABA B R)抗体相关的自身免疫性脑炎合并边缘叶脑炎(LE)患者。我们报告了一系列汉族患者,以进一步完善临床特征。
对北京协和医院脑炎及副肿瘤综合征项目中患者的血清和脑脊液(CSF)样本进行间接免疫荧光检测。回顾性分析抗GABA B R抗体阳性患者的临床资料,并进行描述性统计分析。
18例抗GABA B R抗体阳性病例均有边缘叶综合征,脑电图(EEG)或神经影像学证据符合LE诊断标准。4例患者血清中还存在抗Hu抗体,1例患者血清和脑脊液中均存在抗N-甲基-D-天冬氨酸受体抗体。17例(17/18)患者出现新发难治性癫痫或癫痫持续状态。12例(12/18)患者有记忆缺陷,11例(11/18)患者有性格改变,7例(7/18)患者有意识障碍,3例(3/18)患者有小脑功能障碍。1例LE患者有进行性运动和感觉性多发性神经病。6例(6/18)患者检测出肺癌。10例(10/18)患者磁共振成像显示双侧或单侧中颞叶区域异常。10例(10/18)患者脑电图有颞叶癫痫活动,伴或不伴有广泛性慢波。17例患者接受了免疫治疗,其中15例神经功能有改善。4例肺癌患者在1至12个月内因肿瘤并发症死亡。
我们的研究表明,大多数汉族抗GABA B R抗体相关LE患者有明显的难治性癫痫,免疫治疗后神经功能有改善。合并肺部肿瘤的患者预后相对较差。对于可能患有LE或病因不明的新发癫痫患者,检测抗GABA B R抗体很有必要。