Thakolwiboon Smathorn, Karukote Amputch, Sohn Gyeongmo, Duarte-Celada Walter R, Julayanont Parunyou
Department of Neurology, Texas Tech University Health Sciences CenterLubbockTexas.
Proc (Bayl Univ Med Cent). 2020 Jan 9;33(2):278-280. doi: 10.1080/08998280.2019.1709117. eCollection 2020 Apr.
Autoimmune encephalopathy is one of the treatable causes of rapidly progressive dementia; however, it is often underdiagnosed. Autoantibodies against voltage-gated calcium channel (VGCC) have been linked to several neurological disorders, including Lambert-Eaton syndrome, but VGCC antibody-associated encephalopathy is uncommon. Herein, we present a case of a 74-year-old woman with prominent neuropsychiatric symptoms followed by rapid cognitive decline. Extensive initial studies were nondiagnostic. Subsequently, serum N-type VGCC antibody was positive. After treatment with intravenous immunoglobulin, the patient's cognition and neuropsychiatric symptoms significantly improved.
自身免疫性脑病是快速进展性痴呆的可治疗病因之一;然而,它常常被漏诊。抗电压门控钙通道(VGCC)自身抗体与多种神经系统疾病有关,包括兰伯特-伊顿综合征,但VGCC抗体相关的脑病并不常见。在此,我们报告一例74岁女性患者,该患者有明显的神经精神症状,随后出现快速认知衰退。最初的广泛检查未明确诊断。随后,血清N型VGCC抗体呈阳性。经静脉注射免疫球蛋白治疗后,患者的认知和神经精神症状明显改善。