Acute Onset of Creutzfeldt-Jakob Disease Resembling Stroke in Absence of Diagnostic EEG Findings

Erika Juliani, Matthew Calestino
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Abstract

We report a case of Creutzfeldt-Jakob disease with acute onset of symptoms with EEG negative for PSWC, resembling a cerebrovascular accident. The patient was diagnosed with sporadic CJD by positive RT-QUIC, positive 14-3-3 protein, T-Tau protein of 14560 pg/mL, brain magnetic resonance imaging (MRI) demonstrating restricted diffusion on DWI in bilateral frontal, temporal, occipital cortex, caudate and putaminal nuclei, as well as T2 FLAIR hyperintensities in the bilateral cerebral cortex and basal ganglia. The entire course of the disease from onset to death was 52 days.
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在没有脑电图诊断结果的情况下,克雅氏病急性发作类似中风
我们报告了一例克雅氏病病例,患者急性发病,脑电图显示 PSWC 阴性,类似于脑血管意外。患者的 RT-QUIC 阳性,14-3-3 蛋白阳性,T-Tau 蛋白为 14560 pg/mL,脑磁共振成像(MRI)显示双侧额叶、颞叶、枕叶皮层、尾状核和普特曼核的 DWI 弥散受限,以及双侧大脑皮层和基底节的 T2 FLAIR 高密度,因此被诊断为散发性克雅氏病。从发病到死亡的整个病程为52天。
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