AI Article Synopsis

  • Hypnopompic seizures, which emerge upon waking from sleep, are rare and difficult to diagnose, often requiring advanced EEG techniques for localization.
  • A case study of a 23-year-old male with drug-resistant epilepsy revealed that his hypnopompic seizures originated in the mesial orbitofrontal cortex and involved other brain areas, leading to apnea shortly after the seizures started.
  • The patient's surgical treatment targeting the affected brain regions has resulted in over seven months of being seizure-free, highlighting both the effectiveness of stereotactic EEG in identifying seizure foci and the potential neuroanatomical insights gained from this case about seizure mechanisms.

Article Abstract

Hypnopompic seizures, characterized by arousal from sleep as the primary clinical manifestation, are a rare and challenging seizure type. Their exact localization has been elusive, often requiring stereotactic EEG (SEEG) for accurate identification. We present the case of a 23-year-old male with drug-resistant focal epilepsy, in whom hypnopompic seizures were localized to the mesial orbitofrontal cortex, with rapid recruitment of the middle temporal gyrus, fusiform gyrus, rostral cingulate, and amygdala. SEEG captured multiple seizures, with arousal occurring 4-5 s after EEG onset, followed by ictal central apnea. The patient underwent resection of the right orbitofrontal and mesial temporal lobe regions and has remained seizure-free for over seven months. This case provides new insights into the neuroanatomical origins of seizure-induced arousal, identifying the mesial orbitofrontal cortex as a potential site for hypnopompic seizures. The findings underscore the critical role of SEEG in accurately localizing seizure foci in complex epilepsy cases, enabling targeted surgical interventions. Additionally, we discuss the orbitofrontal cortex's role as a site for extra-thalamic arousal pathways, offering new perspectives on the mechanisms underlying hypnopompic seizures.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11621591PMC
http://dx.doi.org/10.1016/j.ebr.2024.100729DOI Listing

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Article Synopsis
  • Hypnopompic seizures, which emerge upon waking from sleep, are rare and difficult to diagnose, often requiring advanced EEG techniques for localization.
  • A case study of a 23-year-old male with drug-resistant epilepsy revealed that his hypnopompic seizures originated in the mesial orbitofrontal cortex and involved other brain areas, leading to apnea shortly after the seizures started.
  • The patient's surgical treatment targeting the affected brain regions has resulted in over seven months of being seizure-free, highlighting both the effectiveness of stereotactic EEG in identifying seizure foci and the potential neuroanatomical insights gained from this case about seizure mechanisms.
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We report the case of a 43-year-old woman presenting with nocturnal episodes of pain and screaming during sleep starting at age 30. There was no childhood or family history of parasomnia. The events had gradually become more frequent over the years, occurring in the first half of the night within 2 h of sleep onset.

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