Purpose: To investigate the clinical characteristics and surgical outcomes in patients with unilateral hippocampal sclerosis whose scalp ictal EEG recordings localize to the opposite temporal lobe. Methods: We retrospectively reviewed the data of all adult patients who had undergone depth electrode implantation for suspected temporal lobe epilepsy (TLE) at UCLA (1993-2000) or the Montreal Neurological Institute (1991-1998) to identify patients who had (a) unilateral hippocampal atrophy, and (b) surface ictal recordings in which the majority of seizures appeared to initiate in the opposite temporal lobe, with few or none that were concordant with the hippocampal atrophy. Results: Of 109 patients with suspected TLE who underwent depth electrode study at the two centers, five patients met the aforementioned criteria. Four of these five had very severe hippocampal atrophy, whereas the fifth had mild atrophy but extensive signal change on magnetic resonance imaging (MRI). Depth electrode recordings in four of the five patients yielded clear ictal onset in the mesial temporal lobe ipsilateral to the imaging abnormality (contralateral to apparent scalp ictal onset) One patient had an unusual bitemporal onset pattern, which was nonetheless suggestive of onset in the sclerotic hippocampus. No patient had intracranial ictal onset contralateral to the imaging abnormality. All patients underwent resection of the structurally abnormal temporal lobe. After follow-up of >2 years, four (80%) of five patients were seizure free, while the fifth showed lesser improvement (class III). Conclusions: Some patients with severe hippocampal sclerosis (sometimes called a "burned-out hippocampus") have atypical spread of ictal discharges, resulting in apparent gross discordance between imaging and scalp ictal recordings. These patients nonetheless have excellent surgical outcomes on the whole. Whether such patients may forego intracranial recordings requires further study.
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Noe, Francesco
Cattalini, Alessandro
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Cattalini, Alessandro
Verde, Diogo Vila
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Verde, Diogo Vila
Alessi, Camilla
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Alessi, Camilla
Colciaghi, Francesca
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Colciaghi, Francesca
Figini, Matteo
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Fdn IRCCS Ist Neurol Carlo Besta, Sci Direct, Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Figini, Matteo
Zucca, Ileana
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Fdn IRCCS Ist Neurol Carlo Besta, Sci Direct, Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy
Zucca, Ileana
de Curtis, Marco
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Fdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, ItalyFdn IRCCS Ist Neurol Carlo Besta, Epilepsy Unit, Via Celoria 11, I-20133 Milan, Italy