Electroclinical characteristics, genetic findings, and complex epilepsy surgery outcomes in children with low‐grade epilepsy‐associated tumors: A comprehensive view
OBJECTIVE: To evaluate outcomes in relation to epilepsy characteristics and genetic findings in pediatric patients with isolated low-grade epilepsy-associated tumors (LEAT) and LEAT plus focal cortical dysplasia type IIIb (FCD IIIb) who underwent epilepsy surgery. METHODS: Patients younger than 19 years at the time of surgery, with isolated LEAT or LEAT plus FCD IIIb, and a minimum follow-up of 2 years were included. Clinical, neuroimaging, EEG, neuropsychological, surgical, histopathological, and molecular-genetic data were analyzed. Outcomes and potential predictors were assessed across four domains: seizures, antiseizure medication (ASM) use, cognition (Full Scale Intelligence Quotient, FS-IQ), and postoperative surgical complications. RESULTS: Seventy-one children fulfilled the inclusion criteria. Fifty-one (71.8%) had drug-resistant epilepsy. LEAT plus FCD IIIb were more frequent (43/71, 60.6%) than isolated LEAT (28/71, 39.4%). Gangliogliomas were the most common tumor type (39/71, 54.9%), followed by dysembryoplastic neuroepithelial tumors (16/71, 22.5%). Genetic testing demonstrated internal tandem duplication of the FGFR1 gene in most isolated LEAT cases (OR 11.9, 95% CI 1.32-100, p = .02), while LEAT+FCD IIIb cases were more frequently negative (OR 3.8, 95% CI 1.3-10.9, p = .02). After a median 5.7-year follow-up, 64 patients (90.1%) were seizure-free, and 55 (77.5%) discontinued ASM. Earlier seizure onset, longer epilepsy duration, and a higher number of ASM correlated with lower pre- and postoperative FS-IQ. A postoperative FS-IQ gain of >15 points occurred in four patients (7.7%). Two patients (2.8%) had unexpected permanent deficits, and 10 (14.1%) had minor temporary deficits. SIGNIFICANCE: Epilepsy surgery leads to high rates of freedom from seizures and ASM in pediatric patients with LEAT and LEAT + FCD IIIb. Early surgical intervention can be associated with higher pre- and postoperative FS-IQ. Molecular-genetic findings suggest distinct neoplastic and dysplastic entities of LEAT and LEAT plus FCD IIIb.
Authors
- Michal Tichý
- Barbora Straka (ORCID: https://orcid.org/0000-0001-8448-2833)
- Alena Jahodová
- Miroslav Koblížek (ORCID: https://orcid.org/0000-0002-8422-732X)
- Alice Maulisová (ORCID: https://orcid.org/0000-0001-7026-8238)
- Martin Kudr (ORCID: https://orcid.org/0000-0001-7853-3446)
- Radek Janča (ORCID: https://orcid.org/0000-0003-0825-1069)
- Petr Libý (ORCID: https://orcid.org/0000-0001-8392-795X)
- Martina Strnadová (ORCID: https://orcid.org/0009-0001-3997-6436)
- Anežka Bělohlávková (ORCID: https://orcid.org/0000-0001-8462-6892)
- Kateřina Bukačová (ORCID: https://orcid.org/0000-0002-6124-1583)
- Petr Ježdík (ORCID: https://orcid.org/0000-0001-8932-0497)
- Lenka Krsková
- Pavel Kršek (ORCID: https://orcid.org/0000-0002-5740-3690)
- Josef Zámečník
- Zuzana Holubová (ORCID: https://orcid.org/0009-0000-4046-4473)
- Gonzalo Alonso Ramos Rivera (ORCID: https://orcid.org/0009-0003-4184-0321)
- Michal Zápotocký (ORCID: https://orcid.org/0000-0002-9013-2546)
- Martin Kynčl (ORCID: https://orcid.org/0000-0001-6210-6351)
- Vladimír Beneš (ORCID: https://orcid.org/0000-0002-7269-0392)
Institutions
- Charles University (CZ)
- University Hospital Bratislava (SK)
- University Hospital in Motol (CZ)
- Czech Technical University in Prague (CZ)
- Comenius University Bratislava (SK)
Publication Details
- Journal
- Epileptic Disorders
- Published
- 2026-05-27
- DOI
- https://doi.org/10.1002/epd2.70251
- Primary Topic
- Epilepsy research and treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Univerzita Karlova v Praze
- Ministerstvo Zdravotnictví Ceské Republiky