Epilepsy and Behavior Case Reports (Jan 2015)

A case of autoimmune epilepsy associated with anti-leucine-rich glioma inactivated subunit 1 antibodies manifesting electrical shock-like sensations and transparent sadness

  • Yoshiko Murata,
  • Osamu Watanabe,
  • Go Taniguchi,
  • Daichi Sone,
  • Mao Fujioka,
  • Mitsutoshi Okazaki,
  • Eiji Nakagawa,
  • Yutaka Watanabe,
  • Masako Watanabe

DOI
https://doi.org/10.1016/j.ebcr.2015.08.004
Journal volume & issue
Vol. 4, no. C
pp. 91 – 93

Abstract

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Autoimmune epilepsy is an isolated phenotype of autoimmune encephalitis, which may be suspected in patients with unexplained adult-onset seizure disorders or resistance to antiepileptic drugs (AEDs). Antibodies against leucine-rich glioma inactivated subunit 1 of the voltage-gated potassium channel (VGKC) complex, recently termed anti-LGI-1 antibodies, are one of the causes of autoimmune epilepsies. Bizarre symptoms with extremely short duration and high frequency are clues to the possible presence of autoimmune epilepsy with anti-LGI-1 antibodies. Precise diagnosis is important because autoimmune epilepsy is treatable and the prognosis can be predicted.

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