Coexistence of childhood absence epilepsy and benign epilepsy with centrotemporal spikes: A case series

Autor: Federico Mecarini, Giancarlo Di Gennaro, Pasquale Parisi, Victoria Elisa Rinaldi, Anthony J. Ritaccio, Renato D'Alonzo, Sara Casciato, Pasquale Striano, Nelia Zamponi, Salvatore Savasta, Marco Carotenuto, Alberto Verrotti, Alberto Spalice
Přispěvatelé: Verrotti, Alberto, Casciato, Sara, Spalice, Alberto, Carotenuto, Marco, Striano, Pasquale, Parisi, Pasquale, Zamponi, Nelia, Savasta, Salvatore, Rinaldi, Victoria Elisa, D'Alonzo, Renato, Mecarini, Federico, Ritaccio, Anthony J., Di Gennaro, Giancarlo
Rok vydání: 2016
Předmět:
Childhood epilepsy
Male
Pediatrics
medicine.medical_specialty
Benign epilepsy with centrotemporal spikes (BECTS)
Idiopathic generalized epilepsy
pediatrics
Adolescent
Absence seizures
benign epilepsy with centrotemporal spikes (BECTS)
childhood absence epilepsy (CAE)
idiopathic generalized epilepsy
adolescent
child
epilepsy
absence

epilepsy
rolandic

female
humans
male
Prognosis
pediatrics
perinatology and child Health

neurology (clinical)
Anticonvulsant therapy
Absence seizure
030218 nuclear medicine & medical imaging
03 medical and health sciences
Epilepsy
0302 clinical medicine
Childhood absence epilepsy
Medicine
Humans
absence
Childhood absence epilepsy (CAE)
Child
business.industry
General Medicine
rolandic
medicine.disease
Epilepsy
Rolandic

Epilepsy
Absence

Anesthesia
Benign epilepsy
Pediatrics
Perinatology and Child Health

epilepsy
Female
perinatology and child Health
Good prognosis
Neurology (clinical)
Age of onset
business
030217 neurology & neurosurgery
Zdroj: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 21(3)
ISSN: 1532-2130
Popis: Aim Childhood absence epilepsy (CAE) and benign childhood epilepsy with centrotemporal spikes (BECTS) are the most common forms of childhood epilepsy. Recent studies in animal models suggest that the two phenotypes may represent a neurobiological continuum. Although the coexistence of CAE and BECTS has been reported, this issue remains controversial. The purpose of this study was to analyse the electro-clinical characteristics of a group of children with contemporary or subsequent features of absence seizures and focal seizures consistent with BECTS. Material and methods A systematic record review from 8 epilepsy centres was used to identify 11 subjects, 5 females and 6 males, with electro-clinical documented consecutive or contemporary coexistence of CAE and BECTS. Results Patient's age ranged between 7.8 and 17.3 years. Four out of 11 patients presented concomitant features of both syndromes, whereas the remaining 7 experienced the two syndromes at different times. Conclusions Although CAE and BECTS are clearly defined syndromes and considered very different in terms of their pathophysiology, they share some features (such as similar age of onset, overall good prognosis), and can occur in the same patient. The long term prognosis of these patients seems to be good with an excellent response to anticonvulsant therapy.
Databáze: OpenAIRE