| Literature DB >> 32313488 |
Smathorn Thakolwiboon1, Amputch Karukote1, Gyeongmo Sohn1, Walter R Duarte-Celada1, Parunyou Julayanont1.
Abstract
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.Entities:
Keywords: Autoimmune encephalopathy; N-type voltage-gated calcium channel; VGCC encephalitis; rapidly progressive dementia
Year: 2020 PMID: 32313488 PMCID: PMC7156000 DOI: 10.1080/08998280.2019.1709117
Source DB: PubMed Journal: Proc (Bayl Univ Med Cent) ISSN: 0899-8280