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Atypical neuroimaging findings with involvement of brainstem and cerebellum as well as basal ganglia in a case of SSPE misinterpreted as glioma

机译:在SSPE被误认为是神经胶质瘤的情况下,非典型的神经影像学表现与脑干,小脑以及基底神经节有关

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摘要

Subacute sclerosing panencephalitis (SSPE) is a progressive central nervous system disorder, presents after a latent period of 6 years or more from an acute measles infection and has an insidious onset of neurological dysfunction associated with myoclonus and seizure activity. It progresses to coma and death within 1 or 2 years of onset. Brain magnetic resonance imaging (MRI) in SSPE shows lesions usually involving the parieto-occipital and cortico-subcortical regions asymmetrically in the early stage. In later stage of SSPE, symmetric periventricular white-matter changes become more prominent on MRI. Here we describe a case report of a child with SSPE with brain MRI showing extensive brainstem and cerebellum involvement with additional lesion in the basal ganglia, these findings are rarely described with SSPE, and hence low-grade glioma was initially reported by radiologist. Thus, one has to be aware of such extensive brainstem and cerebellum involvement on MRI in SSPE.
机译:亚急性硬化性全脑炎(SSPE)是一种进行性中枢神经系统疾病,在急性麻疹感染潜伏期6年或更长时间后出现,并具有与肌阵挛和癫痫发作相关的神经功能障碍的隐匿性发作。在发病后1或2年内会发展为昏迷和死亡。 SSPE中的脑磁共振成像(MRI)显示病变通常在早期阶段不对称地累及顶枕和皮层下皮质区域。在SSPE的后期,MRI上对称性心室白质的变化变得更加明显。在这里,我们描述了一例SSPE患儿的脑部MRI病例,显示广泛的脑干和小脑受累并伴有基底节的额外病变,SSPE很少描述这些发现,因此低级神经胶质瘤最初是由放射科医生报告的。因此,必须意识到SSPE中MRI广泛涉及脑干和小脑。

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