Bansal Lalit R
Division of Neurology, Children's Mercy Hospital, Kansas City, MO, USA.
Child Neurol Open. 2018 Apr 15;5:2329048X18770576. doi: 10.1177/2329048X18770576. eCollection 2018.
An 11-month-old male presented with acute gastroenteritis, seizures, and altered mental status. Laboratory workup revealed serum sodium of 177 mmol/L. Magnetic resonance imaging of the brain showed reduced diffusion in the supratentorial white matter, T2 hyperintensities in the left central pons and midbrain, subacute stroke in the right occipital lobe, and bilateral cerebellar hemorrhagic infarcts. The child was presumed to have hypernatremia-induced central pontine and extrapontine myelinolysis. He received 5 days of high-dose methylprednisolone for persistent encephalopathy and spastic quadriparesis with rapid recovery of his cognitive function and neurological examination. The child remained seizure-free and achieved normal development at 3-month and 2-year follow-ups. Osmotic demyelination of infancy may leave children with a significant neurological deficit. For favorable neurological outcome, early steroids should be considered.
一名11个月大的男性患儿出现急性胃肠炎、癫痫发作和精神状态改变。实验室检查显示血清钠为177 mmol/L。脑部磁共振成像显示幕上白质弥散受限,左侧脑桥中部和中脑T2高信号,右侧枕叶亚急性卒中,以及双侧小脑出血性梗死。该患儿被推测患有高钠血症诱导的中枢性脑桥和脑桥外髓鞘溶解症。他接受了5天高剂量甲泼尼龙治疗持续性脑病和痉挛性四肢瘫,认知功能和神经检查迅速恢复。在3个月和2年的随访中,该患儿未再发生癫痫发作,发育正常。婴儿期渗透性脱髓鞘可能会使儿童出现严重的神经功能缺损。为获得良好的神经学预后,应考虑早期使用类固醇。