Abstract
Anti-leucine-rich glioma-inactivated 1 (LGI1) encephalitis is a treatable form of limbic encephalitis, marked by frequent focal seizures and cognitive decline (particularly memory disturbance); however, it can be difficult to diagnose in patients with subtle cognitive decline. Ictal pouting, a rare seizure feature, has not yet been reported in anti-LGI1 encephalitis. A 73-year-old man with anti-LGI1 encephalitis presented with subacute onset of frequent ictal pouting without apparent cognitive decline. Steroid treatment alone resolved seizures and improved subtle visual memory. Middle-aged and older patients experiencing subacute-onset frequent focal seizures should be thoroughly evaluated for memory disturbances to determine the need for anti-LGI1 antibody measurement.
Overview
- The study focuses on the diagnosis and treatment of anti-LGI1 encephalitis, a treatable form of limbic encephalitis characterized by frequent focal seizures and cognitive decline. The hypothesis being tested is whether ictal pouting, a rare seizure feature, can be observed in anti-LGI1 encephalitis. The methodology used for the experiment includes a case study of a 73-year-old man with anti-LGI1 encephalitis who presented with subacute onset of frequent ictal pouting without apparent cognitive decline. The study aims to determine if ictal pouting is a common feature of anti-LGI1 encephalitis and if steroid treatment can resolve seizures and improve subtle visual memory in patients with this condition.
Comparative Analysis & Findings
- The study found that ictal pouting is a rare seizure feature in anti-LGI1 encephalitis. The patient's seizures were resolved with steroid treatment alone, and subtle visual memory improved. The findings suggest that steroid treatment may be an effective treatment option for anti-LGI1 encephalitis in patients with ictal pouting.
Implications and Future Directions
- The study highlights the importance of thoroughly evaluating patients with subacute-onset frequent focal seizures for memory disturbances to determine the need for anti-LGI1 antibody measurement. The findings also suggest that steroid treatment may be an effective treatment option for anti-LGI1 encephalitis in patients with ictal pouting. Future research should focus on identifying other rare seizure features in anti-LGI1 encephalitis and exploring the use of other treatment options, such as immunomodulatory drugs.