Suppr超能文献

急性小脑炎还是感染后脑小脑共济失调?急性小脑炎的临床和影像特征。

Acute Cerebellitis or Postinfectious Cerebellar Ataxia? Clinical and Imaging Features in Acute Cerebellitis.

机构信息

Department of Pediatric Neurology, Konya Research and Training Hospital, Konya, Turkey.

Department of Radiology, Hacettepe University Hospitals, Ankara, Turkey.

出版信息

J Child Neurol. 2020 May;35(6):380-388. doi: 10.1177/0883073820901407. Epub 2020 Mar 12.

Abstract

Acute cerebellitis is a rare condition often considered within the group of acute postinfectious cerebellar ataxia despite its distinctive clinical and imaging features. We retrieved clinical, laboratory, and follow-up data of 15 children diagnosed with acute cerebellitis in our department between 2011 and 2019. There were 10 boys and 5 girls aged 3-15 years, median 9.5 years. The most common first symptoms were ataxia, vomiting, and headache. Magnetic resonance imaging (MRI) generally showed bilateral symmetrical T2 hyperintense changes with moderate swelling in the cerebellar cortex. Tonsillar herniation was present in 73.3% and obstructive hydrocephalus in 26.6%. Etiologic workup for infectious pathogens revealed , influenza A virus, cytomegalovirus, and varicella zoster virus in 1 case each. Fourteen of 15 patients were treated with intravenous and/or oral steroids and 8 cases with intravenous immunoglobulin. No patient required surgical decompression. Neurologic examination median 12 months later revealed ataxia and dysmetria in 4 cases (27%), accompanied by memory difficulties, dysarthria or tremor. Follow-up magnetic resonance imaging (MRI; n = 12) showed diffuse cerebellar cortical T2-hyperintense signal changes in 11 cases and cerebellar atrophy in 9. The diagnosis of acute cerebellitis rather than acute postinfectious cerebellar ataxia should be considered when headache and vomiting accompany ataxia in a child. Acute cerebellitis heals with sequelae in about one-third of cases. The absence of fatalities in our series suggests early diagnosis, and steroid treatment can increase the chance of recovery. MRI results were not found to be predictive of outcome.

摘要

急性小脑炎是一种罕见的疾病,尽管其具有独特的临床和影像学特征,但通常仍被归类为急性感染后小脑共济失调。我们检索了 2011 年至 2019 年期间在我科诊断为急性小脑炎的 15 例儿童的临床、实验室和随访资料。其中男 10 例,女 5 例,年龄 3-15 岁,中位数 9.5 岁。最常见的首发症状为共济失调、呕吐和头痛。磁共振成像(MRI)一般显示双侧对称小脑皮质 T2 高信号改变,伴中度肿胀。73.3%的患者存在扁桃体疝,26.6%的患者存在梗阻性脑积水。对感染病原体的病因学检查发现,1 例患者分别感染了甲型流感病毒、巨细胞病毒和水痘带状疱疹病毒。15 例患者中有 14 例接受了静脉和/或口服类固醇治疗,8 例接受了静脉免疫球蛋白治疗。无患者需要手术减压。12 个月后的神经学检查显示,4 例(27%)患者存在共济失调和运动失调,伴有记忆力困难、构音障碍或震颤。12 例患者中有 11 例的随访 MRI 显示弥漫性小脑皮质 T2 高信号改变,9 例患者存在小脑萎缩。当儿童出现共济失调伴头痛和呕吐时,应考虑急性小脑炎而非急性感染后小脑共济失调的诊断。大约三分之一的病例会遗留后遗症。本系列病例中无死亡病例,这表明早期诊断,类固醇治疗可以增加恢复的机会。MRI 结果与预后无关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验