Department of Pediatric Neurology, Fukuoka Children's Hospital.
Department of Radiology, Graduate School and Faculty of Medicine, University of Tokyo.
Clin Infect Dis. 2018 Feb 10;66(5):653-664. doi: 10.1093/cid/cix860.
Acute flaccid myelitis (AFM) is an acute flaccid paralysis syndrome with spinal motor neuron involvement of unknown etiology. We investigated the characteristics and prognostic factors of AFM clusters coincident with an enterovirus D68 (EV-D68) outbreak in Japan during autumn 2015.
An AFM case series study was conducted following a nationwide survey from August to December 2015. Radiographic and neurophysiologic data were subjected to centralized review, and virology studies were conducted for available specimens.
Fifty-nine AFM cases (58 definite, 1 probable) were identified, including 55 children and 4 adults (median age, 4.4 years). The AFM epidemic curve showed strong temporal correlation with EV-D68 detection from pathogen surveillance, but not with other pathogens. EV-D68 was detected in 9 patients: 5 in nasopharyngeal, 2 in stool, 1 in cerebrospinal fluid (adult case), and 1 in tracheal aspiration, nasopharyngeal, and serum samples (a pediatric case with preceding steroid usage). Cases exhibited heterogeneous paralysis patterns from 1- to 4-limb involvement, but all definite cases had longitudinal spinal gray matter lesions on magnetic resonance imaging (median, 20 spinal segments). Cerebrospinal fluid pleocytosis was observed in 50 of 59 cases (85%), and 8 of 29 (28%) were positive for antiganglioside antibodies, as frequently observed in Guillain-Barré syndrome. Fifty-two patients showed variable residual weakness at follow-up. Good prognostic factors included a pretreatment manual muscle strength test unit score >3, normal F-wave persistence, and EV-D68-negative status.
EV-D68 may be one of the causative agents for AFM, while host susceptibility factors such as immune response could contribute to AFM development.
急性弛缓性脊髓炎(AFM)是一种急性弛缓性瘫痪综合征,其病因不明,涉及脊髓运动神经元。我们研究了 2015 年秋季日本与肠道病毒 D68(EV-D68)流行同时发生的 AFM 聚集的特征和预后因素。
2015 年 8 月至 12 月,进行了一项全国性调查后,开展了一项 AFM 病例系列研究。对影像学和神经生理学数据进行了集中审查,并对可用标本进行了病毒学研究。
共发现 59 例 AFM 病例(58 例确诊,1 例可能),包括 55 例儿童和 4 例成人(中位年龄 4.4 岁)。AFM 流行曲线与病原体监测中 EV-D68 的检出具有很强的时间相关性,但与其他病原体无关。9 例患者中检测到 EV-D68:5 例鼻咽,2 例粪便,1 例脑脊液(成人病例),1 例气管抽吸物、鼻咽和血清样本(1 例儿科病例在发病前使用了类固醇)。病例表现为从 1 肢到 4 肢受累的不同瘫痪模式,但所有确诊病例的磁共振成像(MRI)上均存在纵向脊髓灰质病变(中位数 20 个脊髓节段)。59 例中的 50 例(85%)有脑脊液白细胞增多,29 例中的 8 例(28%)抗神经节苷脂抗体阳性,与吉兰-巴雷综合征一样常见。52 例患者在随访时表现出不同程度的残留无力。良好的预后因素包括治疗前徒手肌力测试单位评分>3、F 波持续存在和 EV-D68 阴性。
EV-D68 可能是 AFM 的致病因子之一,而宿主易感性因素(如免疫反应)可能导致 AFM 的发生。