Hongzhi Guan, Weize Kong, Bin Peng, Yan Huang, Qiang Lu, Yuan Jing, Qing Liu, Hang Shen, Haitao Ren, Yicheng Zhu, Dawei Sun, Liying Cui
Zhonghua Yi Xue Za Zhi. 2015 Apr 7;95(13):996-1001.
With the discovery of more patients with anti-N-methyl-D-aspartate (anti- NMDAR) encephalitis, frequent clinical relapses pose a new challenge to neurologists.
Retrospective reviews were conducted for 16 hospitalized patients with relapsing anti-NMDAR encephalitis at our hospital from June 2011 until November 2014. Their clinical data including symptoms, cerebrospinal fluid (CSF) profiles, neuroimaging findings and relapsing treatment were compared with those initial episodes.
There were 11 females and 5 males with a mean onset time of 21.2 (10-34) years. For initial episodes, the mean number of major symptoms was 5. 8 and the mean modified Rankin score (mRS) 4.56. And 7 (43.8%) cases were admitted into intensive care unit (ICU). All received first-line immunotherapy and only one case second-line immunotherapy. Ovarian teratoma was detected and resected in only one case of initial episode. Among 32 relapses, 8 cases (50% ) had multiple (2-4) relapses. There was a median delay of 5.0 (0.5-18) months for relapses. Relapses were common upon pausing or reducing immunotherapy, usually monotherapy with corticosteroids. Compared with initial episodes, relapses were less severe (mean mRS 2.69, mean number of symptom 2.59) and only 2 cases were admitted into ICU during relapses. Presentation of relapses were partial symptoms of initial episode. However, two patients had new symptoms of brain stem involvement. Brain magnetic resonance imaging (MRI) of 8 cases showed abnormality initially during initial episode and disappearance at relapses while new lesions appeared in 7 patients including 3 cases with CNS demyelinating features of central nervous system ( CNS) on MRI. The positivity rate of anti-NMDAR antibody was 100% in CSF and 53.1% in sera during relapses. Anti-AQP4 and NMO-Ig were positive in one case with brain stem involvement. All cases received first-line immunotherapy and 12 chronic second-line immunotherapy. Two cases of ovarian teratoma were detected on reassessment during relapse and then resected.
Inadequacy of second-line and chronic immunotherapy, occult teratoma and potential demyelination may contribute to a relapse of anti-NMDAR encephalitis. And its proper management should follow the recommendations of guidelines.
随着越来越多抗N-甲基-D-天冬氨酸受体(抗NMDAR)脑炎患者被发现,频繁的临床复发给神经科医生带来了新的挑战。
对2011年6月至2014年11月在我院住院的16例复发型抗NMDAR脑炎患者进行回顾性分析。将他们的临床资料,包括症状、脑脊液(CSF)检查结果、神经影像学表现及复发治疗情况与首次发病时进行比较。
11例女性,5例男性,平均发病年龄21.2(10 - 34)岁。首次发病时,主要症状平均数量为5.8个,改良Rankin评分(mRS)平均为4.56。7例(43.8%)患者入住重症监护病房(ICU)。所有患者均接受一线免疫治疗,仅1例接受二线免疫治疗。首次发病时仅1例检测到卵巢畸胎瘤并切除。在32次复发中,8例(50%)有多次(2 - 4次)复发。复发的中位延迟时间为5.0(0.5 - 18)个月。在暂停或减少免疫治疗(通常是单用皮质类固醇)时复发常见。与首次发病相比,复发时病情较轻(mRS平均2.69,症状平均数量2.59),复发时仅2例入住ICU。复发表现为首次发病时的部分症状。然而,2例患者有脑干受累的新症状。8例患者的脑磁共振成像(MRI)在首次发病时最初显示异常,复发时消失,而7例患者出现新病灶,其中3例MRI有中枢神经系统(CNS)脱髓鞘特征。复发时脑脊液中抗NMDAR抗体阳性率为100%,血清中为53.1%。1例脑干受累患者抗水通道蛋白4(AQP4)和视神经脊髓炎免疫球蛋白(NMO-Ig)阳性。所有患者均接受一线免疫治疗,12例接受慢性二线免疫治疗。复发时重新评估发现2例卵巢畸胎瘤,随后切除。
二线及慢性免疫治疗不足、隐匿性畸胎瘤和潜在的脱髓鞘可能导致抗NMDAR脑炎复发。其合理管理应遵循指南建议。