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一名14-3-3检测呈阴性、脑电图和磁共振成像非特异性的患者经尸检证实患有克雅氏病。

Autopsy-proven Creutzfeldt-Jakob disease in a patient with a negative 14-3-3 assay and nonspecific EEG and MRI.

作者信息

Donahue J E, Hanna P A, Hariharan S

机构信息

Division of Neuropathology, Department of Pathology, Rhode Island Hospital, Brown University School of Medicine, 593 Eddy Street, Providence, RI 02903, USA.

出版信息

Neurol Sci. 2004 Feb;24(6):411-3. doi: 10.1007/s10072-003-0198-8.

Abstract

Detection of 14-3-3 protein in cerebrospinal fluid (CSF), in combination with findings on electroencephalography (EEG) and magnetic resonance imaging (MRI), is a highly sensitive and specific diagnostic test for sporadic Creutzfeldt-Jakob disease (CJD) in patients premortem. We present a case of classic, sporadic CJD, confirmed on autopsy and by Western blot. However, all routine premorbid testing was negative, the CSF was negative for the 14-3-3 protein, EEG did not show periodic sharp wave complexes (PSWC), and MRI failed to show hyperintense signal in the basal ganglia. Thus, laboratory support for the diagnosis of CJD was not obtained premortem. The chances of all three diagnostic testing modalities to be negative in a single case of sporadic CJD are extremely remote. Autopsy with neuropathologic confirmation remains the only definitive way to make a diagnosis of CJD.

摘要

脑脊液(CSF)中14-3-3蛋白的检测,结合脑电图(EEG)和磁共振成像(MRI)结果,是对散发性克雅氏病(CJD)患者进行生前诊断的高度敏感且特异的检测方法。我们报告一例经尸检和蛋白质印迹法确诊的经典散发性CJD病例。然而,所有发病前的常规检测均为阴性,CSF中14-3-3蛋白检测呈阴性,EEG未显示周期性尖波复合波(PSWC),MRI也未显示基底节区高信号。因此,生前未获得CJD诊断的实验室支持。在单个散发性CJD病例中,所有三种诊断检测方式均为阴性的可能性极小。尸检及神经病理学确诊仍然是诊断CJD的唯一确定性方法。

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