Your browser doesn't support javascript.
loading
Refractory tonic-myoclonic status epilepticus with catamenial recurrence in epilepsy with myoclonic atonic seizures: A case report.
Proietti, Jacopo; Fiorini, Elena; Cantalupo, Gaetano; Fontana, Elena; Lo Barco, Tommaso; Bonin, Cecilia; Bernardina, Bernardo Dalla; Darra, Francesca.
Afiliação
  • Proietti J; UOC Neuropsichiatria Infantile, Dipartimento Materno-Infantile, Azienda Ospedaliero-Universitaria Integrata, Verona, Italy - Full member of ERN EpiCARE.
  • Fiorini E; Innovation biomedicine Section, Department of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
  • Cantalupo G; Center for Research on Epilepsies in Pediatric age (CREP), Verona, Italy.
  • Fontana E; UOC Neuropsichiatria Infantile, Dipartimento Materno-Infantile, Azienda Ospedaliero-Universitaria Integrata, Verona, Italy - Full member of ERN EpiCARE.
  • Lo Barco T; Center for Research on Epilepsies in Pediatric age (CREP), Verona, Italy.
  • Bonin C; UOC Neuropsichiatria Infantile, Dipartimento Materno-Infantile, Azienda Ospedaliero-Universitaria Integrata, Verona, Italy - Full member of ERN EpiCARE.
  • Bernardina BD; Innovation biomedicine Section, Department of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
  • Darra F; Center for Research on Epilepsies in Pediatric age (CREP), Verona, Italy.
Heliyon ; 10(2): e24747, 2024 Jan 30.
Article em En | MEDLINE | ID: mdl-38304836
ABSTRACT
In epilepsy with myoclonic-atonic seizures (EMA), status epilepticus (SE) may occur during the onset phase, uncommonly in post-puberal patients. We report a post-puberal patient with EMA who presented SE with insidious onset and catamenial recurrence. She had a stormy epilepsy onset at 4 years, with tonic seizures, atypical absences, and myoclonic-atonic seizures, in the absence of SE. After the onset phase, sporadic nocturnal tonic seizures persisted and a mild intellectual disability appeared. At the age of 7, after gonadotropin-releasing hormone analog administration due to central precocious puberty, she presented with SE characterized by recurrent atypical absences, tonic seizures, and awareness impairment, which was successfully treated in 4 days. At 11 years, one week before menstruation, the patient presented with analogous SE that lasted 8 days. One week before the subsequent menstruation, she presented again with SE, initially characterized by atypical absences alternating with phases of awareness and motor impairment related to fast low-voltage EEG activity in the central regions; later, tonic and myoclonic seizures occurring even in the awake state increased, and the "atonic-akinetic status" related to fast EEG activity worsened. After conventional antiepileptic drugs had failed to control the seizures, a progestin was added, with subsequent gradual complete recovery.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article