Current role of surgery for tuberous sclerosis complex-associated epilepsy.

Epilepsy Everolimus Imaging Prognostics Surgery Tuberous sclerosis complex (TSC)

Journal

Pediatric investigation
ISSN: 2574-2272
Titre abrégé: Pediatr Investig
Pays: United States
ID NLM: 101731527

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 05 11 2021
accepted: 30 12 2021
entrez: 6 4 2022
pubmed: 7 4 2022
medline: 7 4 2022
Statut: epublish

Résumé

Tuberous sclerosis complex (TSC) is a rare multisystem, autosomal dominant neurocutaneous syndrome in which epilepsy is the most common of several neurological and psychiatric manifestations. Around two thirds of patients develop drug-resistant epilepsy for whom surgical resection of epileptogenic foci is indicated when seizures remain inadequately controlled following trial of two antiseizure medications. The challenge with presurgical and surgical approaches with patients with TSC is overcoming the complexity from the number of tubers and the multiplex epileptogenic network forming the epileptogenic zone. Data suggest that seizure freedom is achieved by 55%-60% of patients, but predictive factors for success have remained elusive, which makes for unconfident selection of surgical candidates. This article presents three different cases as illustrations of the potential challenges faced when assessing the suitability of TSC patients for epilepsy surgery.

Identifiants

pubmed: 35382422
doi: 10.1002/ped4.12312
pii: PED412312
pmc: PMC8960933
doi:

Types de publication

Journal Article

Langues

eng

Pagination

16-22

Informations de copyright

© 2022 Chinese Medical Association. Pediatric Investigation published by John Wiley & Sons Australia, Ltd on behalf of Futang Research Center of Pediatric Development.

Déclaration de conflit d'intérêts

Nicola Specchio has received support from Livanova and Biomarin, and has served as a paid consultant for Livanova. Paolo Curatolo has served as a paid consultant for Novartis. The remaining authors report no conflict of interest.

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Auteurs

Nicola Specchio (N)

Rare and Complex Epilepsy Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Giusy Carfi Pavia (GC)

Rare and Complex Epilepsy Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Luca de Palma (L)

Rare and Complex Epilepsy Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Alessandro De Benedictis (A)

Neurosurgery Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Chiara Pepi (C)

Rare and Complex Epilepsy Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Marta Conti (M)

Rare and Complex Epilepsy Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Carlo Efisio Marras (CE)

Neurosurgery Unit, Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Federico Vigevano (F)

Department of Neurosciences Bambino Gesù Children's Hospital, IRCCS Rome Italy.

Paolo Curatolo (P)

Child Neurology and Psychiatry Unit, Systems Medicine Department Tor Vergata University Rome Italy.

Classifications MeSH