Liang Jennifer, Singhal Ash
Faculty of Medicine and the Division of Neurosurgery, University of British Columbia and British Columbia's Children's Hospital, Vancouver, British Columbia, Canada.
J Neurosurg Pediatr. 2016 May;17(5):537-9. doi: 10.3171/2015.9.PEDS15477. Epub 2016 Jan 8.
Hurler syndrome is the most severe form of mucopolysaccharidosis (MPS) Type 1. Progressive neurocognitive decline in this condition can be accompanied by macrocephaly, ventriculomegaly, and/or periventricular signal changes on MRI, which often leads to a neurosurgical referral. In this case, the authors describe a 2-year-old boy with ventriculomegaly and periventricular T2 signal changes, both of which decreased following medical management of Hurler syndrome. The authors discuss the possible mechanisms for this finding and the implications for neurosurgical treatment of this condition.
黏多糖贮积症 I 型(MPS I)中,Hurler 综合征是最严重的一种形式。在这种疾病中,进行性神经认知功能衰退可能伴有巨头畸形、脑室扩大和/或磁共振成像(MRI)上的脑室周围信号改变,这常常导致患者被转诊至神经外科。在本文病例中,作者描述了一名 2 岁男孩,其存在脑室扩大和脑室周围 T2 信号改变,在对 Hurler 综合征进行药物治疗后,这两种情况均有所减轻。作者讨论了这一发现的可能机制以及对该疾病神经外科治疗的意义。