Yaguchi Hiroshi, Hirai Toshiaki, Kurita Akira, Mochio Soichiro
Department of Neurology, The Jikei University Kashiwa Hospital.
Rinsho Shinkeigaku. 2011 Oct;51(10):774-6. doi: 10.5692/clinicalneurol.51.774.
We report a 55-year-old woman with limbic encephalitis associated with leucine-rich glioma-inactivated 1 (LGI1) antibody. She first developed a generalized seizure, following by consciousness loss. Although anticonvulant was initially effective, she began to present frequently with seizure and memory impairment. After eleven months from onset, she was admitted due to generalized seizure. Neurological examination after recovering from the treatment with anesthetic agent demonstrated disorientation and memory impairment. Cerebrospinal fluid analysis was unremarkable. MR brain FLAIR imaging demonstrated high intensity lesions in the medial parts of the both temporal lobes, suggesting limbic encephalitis. There were no signs of malignant tumor detected on systemic examination. LGI1 antibody was positive in the cerebrospinal fluid and we finally diagnosed this patient as having limbic encephalitis associated with LGI1 antibody. She demonstrated a good response to steroid therapy and was discharged after one month.
我们报告了一名55岁的女性,患有与富含亮氨酸的胶质瘤失活1(LGI1)抗体相关的边缘叶脑炎。她最初出现全身性癫痫发作,随后意识丧失。尽管抗惊厥药物最初有效,但她开始频繁出现癫痫发作和记忆障碍。发病11个月后,她因全身性癫痫发作入院。在使用麻醉剂治疗恢复后进行的神经系统检查显示定向障碍和记忆障碍。脑脊液分析无异常。脑部磁共振成像液体衰减反转恢复序列(MR brain FLAIR)显示双侧颞叶内侧部分有高强度病变,提示边缘叶脑炎。全身检查未发现恶性肿瘤迹象。脑脊液中LGI1抗体呈阳性,我们最终诊断该患者患有与LGI1抗体相关的边缘叶脑炎。她对类固醇治疗反应良好,一个月后出院。