Two Cases of Norovirus Gastroenteritis Associated with Severe Neurologic Complications

Q4 Medicine Annals of Child Neurology Pub Date : 2022-11-07 DOI:10.26815/acn.2022.00262
Myung Ji Yoo, Dong Jun Ha, Dong Hyun Kim, Y. Kwon
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引用次数: 1

Abstract

Norovirus, along with rotavirus, is a common virus that causes gastroenteritis in children [1]. Complications related to norovirus enteritis are rare, and the prognosis is good. However, various clinical features and poor prognoses have been reported in norovirus-associated encephalopathy [2,3]. Herein, we report two pediatric cases of norovirus infection with severe neurologic complications. A 7-year-old girl (patient A) visited the emergency room (ER) of a local hospital for diplopia, impaired vision, eye movement disorder, and mild neck stiffness that had lasted for 5 days. Days before developing ocular symptoms, she had abdominal pain, was diagnosed with enteritis, and took medications to alleviate the symptoms. Her mental status was alert, and the Glasgow Coma Scale score was 15. In a workup at a local hospital, brain magnetic resonance imaging (MRI) and angiography showed papilledema. She received mannitol for papilledema and intravenous methylprednisolone (1 mg/kg/ day) for 4 days for sixth cranial nerve palsy, followed by dexamethasone (0.5 mg/kg/day) for the next 6 days. During hospitalization, transient ataxia and bilateral periorbital pain were noted. Starting on hospitalization day 9, her symptoms improved, and a dexamethasone dose of 0.25 mg/kg/day was administered for 2 days. Subsequently, a reduced dexamethasone dose (0.125 mg/kg/day) was administered for the next 2 days. She was discharged on hospitalization day 13; the dexamethasone dose was tapered for 4 days and discontinued. However, on day 4 after discharge, her symptoms worsened again. Hence, she was transferred to our hospital. On transfer to our hospital, she had fixed dilated pupils, and her left eye had visual acuity of light perception and exhibited left gaze palsy (Fig. 1). Her right eye had a visual acuity of 0.04. On fundoscopy, stage 4 papilledema was confirmed in both eyes, and a slight decrease in the deep tendon reflex was observed. Whole-spine MRI and an autoantibody panel (anti-aquaporin 4 antibody [AQP4], anti-neurofilament antibody [NF], and anti-myelin oligodendrocyte glycoprotein [MOG]) revealed normal findings. Stool virus polymerase chain reaction (PCR) findings showed positivity for norovirus genogroup II (GII). She received intravenous immunoglobulin (IVIG) at a dose of 0.4 g/kg for 5 days and methylprednisolone (30 mg/kg/day) for 3 days. Her abdominal symptoms and visual acuity in the right eye improved. Further improvement was noted after acetazolamide was administered. A previously healthy 8-month-old girl (patient B) was brought to our ER with an ongoing seizure for 20 minutes. The patient had been treated for
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诺如病毒性胃肠炎并发严重神经系统并发症2例
诺如病毒和轮状病毒是一种常见的病毒,可导致儿童肠胃炎[1]。与诺如病毒肠炎相关的并发症很少,预后良好。然而,诺如病毒相关性脑病的各种临床特征和不良预后已有报道[2,3]。在此,我们报告了两例儿童诺如病毒感染并伴有严重神经系统并发症的病例。一名7岁女孩(患者A)因复视、视力受损、眼球运动障碍和持续5天的轻度颈部僵硬而到当地医院急诊室就诊。在出现眼部症状前几天,她曾腹痛,被诊断为肠炎,并服用药物缓解症状。她的精神状态很好,格拉斯哥昏迷量表得分为15分。在当地一家医院的检查中,脑部核磁共振成像(MRI)和血管造影术显示为视乳头水肿。她接受甘露醇治疗视神经乳头水肿,静脉注射甲基强的松龙(1 mg/kg/天)治疗第六脑神经麻痹4天,然后接受地塞米松(0.5 mg/kg/日)治疗6天。住院期间,出现短暂性共济失调和双侧眶周疼痛。从住院第9天开始,她的症状有所改善,地塞米松剂量为0.25 mg/kg/天,持续2天。随后,在接下来的2天内给予减少的地塞米松剂量(0.125mg/kg/天)。她在住院第13天出院;地塞米松剂量逐渐减少4天并停止。然而,出院后第4天,她的症状再次恶化。因此,她被转移到我们医院。在被转移到我们医院时,她有固定的瞳孔扩张,左眼有光感视力,并表现出左视麻痹(图1)。她的右眼视力为0.04。在眼底镜检查中,双眼均确认为4期视乳头水肿,并观察到深肌腱反射轻微减弱。全脊柱MRI和自身抗体组(抗水通道蛋白4抗体[AQP4]、抗神经丝抗体[NF]和抗髓鞘少突胶质细胞糖蛋白[MOG])显示正常结果。粪便病毒聚合酶链式反应(PCR)结果显示诺如病毒基因组II(GII)阳性。她接受了0.4 g/kg剂量的静脉注射免疫球蛋白(IVIG)5天,甲基强的松龙(30 mg/kg/天)3天。她的腹部症状和右眼视力都有所改善。乙酰唑胺给药后有进一步改善。一名先前健康的8个月大女孩(患者B)被带到我们的急诊室,持续癫痫发作20分钟。病人已经接受了
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来源期刊
Annals of Child Neurology
Annals of Child Neurology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
35
审稿时长
8 weeks
期刊最新文献
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