Neurology Department, Hospital Universitario de La Princesa, Madrid, Spain.
Eur J Neurol. 2021 Apr;28(4):1385-1391. doi: 10.1111/ene.14624. Epub 2020 Nov 27.
The aim of our study is to review the relationship between NCSE and sCJD. Creutzfeldt-Jakob disease (CJD) is the most common form of human prion disease. Electroencephalography (EEG)-detected changes such as periodic sharp wave complexes, superimposable to those seen in non-convulsive epileptic status (NCSE), have only rarely been described at CJD onset, especially in sporadic CJD (sCJD) cases.
We describe clinical, EEG, cerebrospinal fluid (CSF) and neuroimaging findings of a confirmed case of sCJD with tau pathology, initially diagnosed as NCSE. We performed a literature review in PubMed of previous publications on both sCJD and NCSE.
An 82-year-old woman with no medical history presented with a 2-week rapidly progressive neurological disorder, with motor aphasia, myoclonus, pyramidalism, and left posterior alien hand. EEG showed periodic sharp waves on right frontal regions, so anti-epileptic treatment was started. CSF results were normal. Brain magnetic resonance imaging demonstrated hyperintensity of the right cerebral cortex in diffusion sequences. Due to suspected new-onset refractory status epilepticus (NORSE), corticosteroid treatment was started, without clinical improvement. Necropsy results confirmed sCJD with tau pathology. The literature review identified 14 references including a total of 18 cases with NCSE as the presenting symptom of sCJD; the clinical and results in complementary tests were compiled into a table.
Sporadic CJD should be considered in the differential diagnosis of patients with rapid cognitive decline and EEG changes consistent with NCSE. The wide heterogeneity in the etiology of NCSE, including autoimmune disorders, especially NORSE, suggests immunotherapy should be initiated based on a good risk-benefit balance. Some cases of sCJD, such as the present case with tau pathology, may mimic this clinico-electrical course.
本研究旨在回顾 NCSE 与 sCJD 之间的关系。克雅氏病(CJD)是最常见的人类朊病毒病。脑电图(EEG)检测到的变化,如周期性尖波复合波,与非惊厥性癫痫持续状态(NCSE)所见相似,仅在 CJD 发病时很少被描述,尤其是在散发性 CJD(sCJD)病例中。
我们描述了一例经证实的 sCJD 伴 tau 病理学患者的临床、EEG、脑脊液(CSF)和神经影像学表现,最初被诊断为 NCSE。我们在 PubMed 上对 sCJD 和 NCSE 的先前出版物进行了文献回顾。
一位 82 岁女性,无既往病史,表现为 2 周快速进展的神经功能障碍,伴有运动性失语、肌阵挛、锥体束征和左侧后天性手生疏。EEG 显示右侧额区周期性尖波,因此开始抗癫痫治疗。CSF 结果正常。脑磁共振成像显示弥散序列右大脑皮质高信号。由于怀疑新发难治性癫痫持续状态(NORSE),开始使用皮质类固醇治疗,但临床无改善。尸检结果证实为 sCJD 伴 tau 病理学。文献回顾确定了 14 篇参考文献,共包括 18 例以 NCSE 为首发症状的 sCJD 病例;将临床表现和补充检查结果汇编成表格。
在快速认知衰退和 EEG 改变与 NCSE 一致的患者的鉴别诊断中,应考虑散发性 CJD。NCSE 的病因广泛存在异质性,包括自身免疫性疾病,尤其是 NORSE,因此应根据良好的风险效益平衡启动免疫治疗。一些 sCJD 病例,如本例伴有 tau 病理学,可能会模仿这种临床电生理过程。