Ong Charlene J, Al-Lozi Muhammad, Cimino Patrick J, Bucelli Robert
Departments of Neurology (CJO, MA-L, RB) and Pathology (PJC), Washington University in St. Louis, St. Louis, MO.
Neurol Clin Pract. 2015 Aug;5(4):326-332. doi: 10.1212/CPJ.0000000000000160.
Creutzfeldt-Jakob disease (CJD) is a fatal, rapidly progressive neurodegenerative disease. Most cases are sporadic (sCJD). The pathogenesis of sCJD is associated with a conformational change in abnormal prion protein causing widespread neuronal degeneration, and clinical manifestations can be quite protean. Peripheral nerve hyperexcitability syndrome (PNHS) is rarely associated with CJD and is more commonly associated with autoimmune/paraneoplastic syndromes associated with antibodies against the voltage-gated potassium channel complex (VGKC-Abs). Reports of PNHS in CJD are rare. We report 2 patients with progressive cognitive decline in the setting of peripheral nerve hyperexcitability on electrodiagnostic testing. In both patients VGKC-Abs were negative, and autopsy confirmed that both had sCJD, VV2 subtype. While uncommon, it is important to consider sCJD in patients presenting with PNHS and rapidly progressive dementia.
克雅氏病(CJD)是一种致命的、快速进展的神经退行性疾病。大多数病例为散发性(sCJD)。sCJD的发病机制与异常朊蛋白的构象改变有关,可导致广泛的神经元变性,其临床表现可能多种多样。周围神经兴奋性增高综合征(PNHS)很少与CJD相关,更常见于与抗电压门控钾通道复合物抗体(VGKC-Abs)相关的自身免疫/副肿瘤综合征。CJD中PNHS的报道很少。我们报告2例在电诊断测试中出现周围神经兴奋性增高且伴有进行性认知功能下降的患者。两名患者的VGKC-Abs均为阴性,尸检证实两人均患有sCJD,VV2亚型。虽然不常见,但对于出现PNHS和快速进展性痴呆的患者,考虑sCJD很重要。