Fischell Stefanie Zaner, Fischell Jonathan, Kliot Tamara, Tumulty Jamie, Thompson Stephen J, Raees Madiha Q
Department of Pediatrics, University of Maryland Medical Center, Baltimore, MD, United States.
Division of Pediatric Neurology, Department of Pediatrics and Neurology, University of Maryland School of Medicine, Baltimore, MD, United States.
Front Neurol. 2023 Sep 1;14:1239746. doi: 10.3389/fneur.2023.1239746. eCollection 2023.
Acute Necrotizing Encephalopathy (ANE) is a condition characterized by symmetric, bilateral lesions affecting the thalamus and potentially other areas of the brain following an acute febrile illness. It manifests clinically as abrupt development of encephalopathy, or alteration in mental status that often includes development of seizures and progression to coma. Treatment strategies combine immunosuppressive therapies and supportive care with varying levels of recovery, however there are no universally accepted, data-driven, treatment algorithms for ANE. We first report a case of a previously healthy 10-year-old female with acute onset diplopia, visual hallucinations, lethargy, and seizures in the setting of subacute non-specific viral symptoms and found to have bilateral thalamic and brainstem lesions on MRI consistent with ANE. She was treated with a combination of immunomodulatory therapies and ultimately had a good outcome. Next, we present a meta-analysis of 10 articles with a total of 158 patients meeting clinical and radiographic criteria for ANE. Each article reported immunosuppressive treatments received, and associated morbidity or mortality outcome for each individual patient. Through our analysis, we confirm the effectiveness of high-dose, intravenous, methylprednisolone (HD-IV-MP) therapy implemented early in the disease course (initiation within 24 h of neurologic symptom onset). There was no significant difference between patients treated with and without intravenous immunoglobulin (IVIG). There was no benefit of combining IVIG with early HD-IV-MP. There is weak evidence suggesting a benefit of IL-6 inhibitor tocilizumab, especially when used in combination with early HD-IV-MP, though this analysis was limited by sample size. Finally, plasma exchange (PLEX) improved survival. We hope this meta-analysis will be useful for clinicians making treatment decisions for patients with this potentially devastating condition.
急性坏死性脑病(ANE)是一种在急性发热性疾病后,以双侧丘脑对称性病变为特征,可能累及大脑其他区域的病症。其临床症状表现为脑病的突然发作,即精神状态改变,常伴有癫痫发作并进展至昏迷。治疗策略包括免疫抑制疗法和支持性护理,恢复程度各不相同,然而目前尚无针对ANE被普遍接受的、基于数据的治疗方案。我们首先报告一例病例,一名既往健康的10岁女性,在亚急性非特异性病毒症状发作时急性起病,出现复视、视幻觉、嗜睡和癫痫发作,MRI检查发现双侧丘脑和脑干病变,符合ANE表现。她接受了免疫调节疗法联合治疗,最终预后良好。接下来,我们对10篇文章进行了荟萃分析,共有158例患者符合ANE的临床和影像学标准。每篇文章都报告了每位患者接受的免疫抑制治疗以及相关的发病率或死亡率结果。通过我们的分析,我们证实了在疾病病程早期(神经症状发作24小时内开始)实施大剂量静脉注射甲泼尼龙(HD-IV-MP)治疗的有效性。接受和未接受静脉注射免疫球蛋白(IVIG)治疗的患者之间没有显著差异。IVIG与早期HD-IV-MP联合使用并无益处。有微弱证据表明白细胞介素-6抑制剂托珠单抗有益,特别是与早期HD-IV-MP联合使用时,不过该分析受样本量限制。最后,血浆置换(PLEX)可提高生存率。我们希望这项荟萃分析对临床医生为患有这种可能具有毁灭性病症的患者做出治疗决策有所帮助。