Literature DB >> 32313488

Rapidly progressive dementia-associated N-type voltage-gated calcium channel antibody encephalopathy.

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.
Copyright © 2020 Baylor University Medical Center.

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


  11 in total

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