• Seizure · Jan 2007

    Epilepsy syndromes associated with hypothalamic hamartomas.

    • Luiz H Castro, Luiz K Ferreira, Leandro R Teles, Carmen L Jorge, Paula R Arantes, Carla R Ono, Carla C Adda, and Rosa F Valerio.
    • Hospital das Clinicas Faculdade de Medicina Universidade de Sao Paulo, Brazil, Neurology, Al. Lorena, 983 apto 82, 01424-904 Sao Paulo, Brazil. castrolh@usp.br
    • Seizure. 2007 Jan 1; 16 (1): 50-8.

    PurposeHypothalamic hamartoma (HH) related epilepsy presents with gelastic seizures (GS), other seizure types and cognitive deterioration. Although seizure origin in GS has been well established, non-GS are poorly characterized. Their relationship with the HH and cognitive deterioration remains poorly understood. We analyzed seizure type, spread pattern in non-GS and their relationship with the epileptic syndrome in HH.MethodsWe documented all current seizure types in six adult patients with HH-epilepsy with video-EEG monitoring, characterized clinical-electrographic features of gelastic and non-gelastic seizures and correlated these findings with cognitive profile, as well as MRI and ictal SPECT data.ResultsOnly four seizure types were seen: GS, complex partial (CPS), tonic seizures (TS) and secondarily generalized tonic-clonic seizures (sGTC). An individual patient presented either CPS or TS, but not both. GS progressed to CPS or TS, but not both. Ictal patterns in GS/TS and in GS/CPS overlapped, suggesting ictal spread from the HH to other cortical regions. Ictal SPECT patterns also showed GS/TS overlap. Patients with GS-CPS presented a more benign profile with preserved cognition and clinical-EEG features of temporal lobe epilepsy. Patients with GS-TS had clinical-EEG features of symptomatic generalized epilepsy, including mental deterioration.ConclusionsVideo-EEG and ictal SPECT findings suggest that all seizures in HH-related epilepsy originate in the HH, with two clinical epilepsy syndromes: one resembling temporal lobe epilepsy and a more catastrophic syndrome, with features of a symptomatic generalized epilepsy. The epilepsy syndrome may be determined by HH size or by seizure spread pattern.

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