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Cortical Hyperintensity on Diffusion-weighted Images as the Presymptomatic Marker of Sporadic Creutzfeldt-Jakob Disease

机译:弥散加权图像上的皮质高强度作为散发性Creutzfeldt-Jakob疾病的症状前标志

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摘要

We herein report a sporadic Creutzfeldt-Jakob disease (sCJD) patient followed from the presymptomatic phase to death. A 67-year-old woman had abnormal hyperintense cortical lesions on diffusion-weighted magnetic resonance imaging (MRI) one year before the onset. The levels of 14-3-3 protein and total tau protein, and findings from a real-time quaking-induced conversion test were normal at first but became abnormal after disease onset. Although there are four reports of presymptomatic sCJD identified by MRI, this is the first case report in which all three biomarkers had been assessed before and after the disease onset. MRI might be the most sensitive modality for detecting presymptomatic sCJD patients.
机译:我们在这里报告了零星的Creutzfeldt-Jakob病(sCJD)患者从症状发生前阶段到死亡。一名67岁的女性在发病前一年通过弥散加权磁共振成像(MRI)出现了异常高强度皮质病变。 14-3-3蛋白和总tau蛋白的水平以及实时地震诱导的转化试验的结果最初是正常的,但在疾病发作后变得异常。尽管有4例通过MRI鉴定出症状前sCJD的报道,但这是第一例病例报告,其中在疾病发作之前和之后都对所有三种生物标志物进行了评估。 MRI可能是检测有症状的sCJD患者最敏感的方式。

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