Zhang Hesheng, Xiong Weixi, Liu Xu, Liu Wenyu, Zhou Dong, Wu Xintong
Department of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Front Neurol. 2022 Apr 12;13:874867. doi: 10.3389/fneur.2022.874867. eCollection 2022.
This study aimed to evaluate the clinical characteristics and long-term surgical outcomes of patients with anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis with teratoma.
Patients who were admitted to West China Hospital from June 2012 to June 2019 and diagnosed with anti-NMDAR encephalitis were enrolled in the study. Medical records were reviewed prospectively to gather clinical characteristic data. Patients were followed up at long-term every 3 months.
This study included 192 patients, among whom 21 (10.9%) were detected with having a teratoma. Patients included 20 women, with a mean age of 24.62 ± 7.61 years. Seizure and psychiatric symptoms were the most dominant symptoms in both groups, followed by memory deficits. Central hypoventilation (52.4 vs. 17%, < 0.001) and decreased consciousness (71.4 vs. 31.3%, = 0.002) were significantly more frequent in patients with teratoma than in those without. Moreover, the anti-NMDAR antibody titer was higher ( = 0.021) and the baseline modified Rankin scale score was lower ( = 0.004) in patients with teratoma than in those without. First-line immunotherapy was performed in 21 (100%) patients with teratoma and 167 (97.7%) patients without teratoma. All patients with teratoma had the tumor removed. During follow-up, two (9.5%) patients with teratoma and 11 (6.4%) patients without teratoma died, whereas 1 (4.8%) patient with teratoma and 37 (21.6%) patients without teratoma had relapses. Overall, 19 (90.5%) patients with teratoma and 151 (88.3%) patients without teratoma achieved favorable clinical outcomes at the final follow-up.
With early detection and removal of teratoma, most patients with anti-NMDAR encephalitis and teratoma achieved a favorable long-term prognosis.
本研究旨在评估合并畸胎瘤的抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎患者的临床特征及长期手术结局。
纳入2012年6月至2019年6月入住华西医院且诊断为抗NMDAR脑炎的患者。前瞻性回顾病历以收集临床特征数据。患者每3个月进行一次长期随访。
本研究纳入192例患者,其中21例(10.9%)检测出患有畸胎瘤。患者包括20名女性,平均年龄为24.62±7.61岁。癫痫和精神症状是两组中最主要的症状,其次是记忆缺陷。合并畸胎瘤的患者中枢性通气不足(52.4%对17%,<0.001)和意识下降(71.4%对31.3%,=0.002)的发生率显著高于未合并畸胎瘤的患者。此外,合并畸胎瘤的患者抗NMDAR抗体滴度更高(=0.021),基线改良Rankin量表评分更低(=0.004)。21例(100%)合并畸胎瘤的患者和167例(97.7%)未合并畸胎瘤的患者接受了一线免疫治疗。所有合并畸胎瘤的患者均切除了肿瘤。随访期间,2例(9.5%)合并畸胎瘤的患者和11例(6.4%)未合并畸胎瘤的患者死亡,而1例(4.8%)合并畸胎瘤的患者和37例(21.6%)未合并畸胎瘤的患者复发。总体而言,19例(90.5%)合并畸胎瘤的患者和151例(88.3%)未合并畸胎瘤的患者在末次随访时获得了良好的临床结局。
通过早期发现并切除畸胎瘤,大多数合并畸胎瘤的抗NMDAR脑炎患者获得了良好的长期预后。