Volume 40, Issue 9 pp. 1312-1315

Benign Childhood Epilepsy with Centrotemporal Spikes and Hippocampal Atrophy

Philippe Gelisse

Philippe Gelisse

Centre Saint Paul, Marseille

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Pierre Genton

Corresponding Author

Pierre Genton

Centre Saint Paul, Marseille

Address correspondence and reprint requests to Dr. P. Genton at Centre Saint Paul, 13258 Marseille 09, France. E-mail: [email protected]Search for more papers by this author
Charles Raybaud

Charles Raybaud

Service de Neuroradiologie CHU Timone, Marseille

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Annick Thiry

Annick Thiry

Service de Pédiatrie, CHG de Bastia, Bastia, France

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Olivier Pincemaille

Olivier Pincemaille

Service de Pédiatrie, CHG de Bastia, Bastia, France

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First published: 02 August 2005
Citations: 18

Presented in part at the 49th meeting of the French League Against Epilepsy, Bordeaux, November 11, 1998.

Abstract

Summary: A boy without significant family or personal history had three consecutive nocturnal seizures at 1-month intervals at age 10 years, all simple focal seizures with motor and sensory symptoms, the last with secondary generalization. Waking and napping EEG showed focal sharp changes typical of benign epilepsy with centrotemporal spikes (BECTS). A magnetic resonance imaging documented a marked right hippocampal atrophy (HA). After valproic acid (VPA) therapy, there were no more seizures, and there were fewer EEG changes. An EEG performed in the younger, fully asymptomatic 8-year-old sister documented unilateral right focal sharp waves. This case shows that HA, as well as other central nervous system lesions, can be found fortuitously in patients with BECTS.

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