Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation

Implications for surgical therapy

Bruno Maton, Pavel Kršek, Prasanna Jayakar, Trevor Resnick, Monica Koehn, Glenn Morrison, John Ragheb, Amilcar Castellano-Sanchez, Michael Duchowny

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Purpose: Anecdotal reports have described cortical malformations in epileptic patients with Sturge-Weber syndrome (SWS). No data are available regarding the prevalence and significance of this association. Methods: We reviewed retrospectively the clinical profile, preoperative magnetic resonance imaging (MRI) studies, and pathology reports of all patients with SWS and medically intractable epilepsy evaluated in our epilepsy surgery program between 1979 and 2006. Results: Twelve patients (male/female = 7/5) were identified. Mean age at seizure onset was 11.1 ± 16.7 months. Seizures occurred daily in seven patients and weekly in five patients. A facial port-wine stain was noted in 10 cases. Eleven patients evidenced developmental delay and eight were hemiparetic. Eight patients underwent excisional surgery for epilepsy (mean age 10.3 ± 6.5 year), including hemispherectomy (n = 4) and focal cortical resection (n = 4). Tissue was available for neuropathology in six operated cases and revealed polymicrogyria (n = 3) and cortical dysplasia (n = 4). Polymicrogyria was associated with cortical dysplasia in one child. Brain MRIs were reviewed in 10 of 12 patients and were consistent with cortical malformations in all cases. Conclusions:Weconclude that cortical malformations are frequent in patients with medically intractable epilepsy and Sturge-Weber-syndrome and may be the primary cause of epilepsy.

Original languageEnglish
Pages (from-to)257-267
Number of pages11
JournalEpilepsia
Volume51
Issue number2
DOIs
StatePublished - Feb 5 2010

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Sturge-Weber Syndrome
Malformations of Cortical Development
Epilepsy
Therapeutics
Seizures
Hemispherectomy
Port-Wine Stain
Drug Resistant Epilepsy
Age of Onset
Magnetic Resonance Imaging
Pathology

Keywords

  • Cortical dysplasia
  • Epilepsy
  • Polymicrogyria
  • Sturge-Weber syndrome
  • Young children

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation : Implications for surgical therapy. / Maton, Bruno; Kršek, Pavel; Jayakar, Prasanna; Resnick, Trevor; Koehn, Monica; Morrison, Glenn; Ragheb, John; Castellano-Sanchez, Amilcar; Duchowny, Michael.

In: Epilepsia, Vol. 51, No. 2, 05.02.2010, p. 257-267.

Research output: Contribution to journalArticle

Maton, B, Kršek, P, Jayakar, P, Resnick, T, Koehn, M, Morrison, G, Ragheb, J, Castellano-Sanchez, A & Duchowny, M 2010, 'Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy', Epilepsia, vol. 51, no. 2, pp. 257-267. https://doi.org/10.1111/j.1528-1167.2009.02304.x
Maton, Bruno ; Kršek, Pavel ; Jayakar, Prasanna ; Resnick, Trevor ; Koehn, Monica ; Morrison, Glenn ; Ragheb, John ; Castellano-Sanchez, Amilcar ; Duchowny, Michael. / Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation : Implications for surgical therapy. In: Epilepsia. 2010 ; Vol. 51, No. 2. pp. 257-267.
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