Surgical outcome and predictive factors in adult patients with intractable epilepsy and focal cortical dysplasia.

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Title: Surgical outcome and predictive factors in adult patients with intractable epilepsy and focal cortical dysplasia.
Authors: Siegel, A. M., Cascino, Gregory D., Meyer, F. B., Marsh, W. R., Scheithauer, B. W., Sharbrough51,3, F. W.
Source: Acta Neurologica Scandinavica. Feb2006, Vol. 113 Issue 2, p65-71. 7p. 2 Charts, 3 Graphs.
Subjects: Epilepsy, Brain diseases, Dysplasia, Temporal lobe, Cerebral cortex
Abstract: Objectives – To determine the surgical outcome and prognostic factors in adult patients with intractable epilepsy and focal cortical dysplasia (FCD). Materials and methods – We retrospectively studied the operative outcome in 21 consecutive adult patients with FCD who underwent surgical treatment for intractable partial epilepsy. Results – The mean age at surgery was 32.7 years (range, 18–58 years). The median post-operative follow-up was 2.5 years. The FCD was extratemporal in 11 patients, involved the temporal lobe in 10 patients, and was multilobar in eight patients. Eleven patients (52%) were rendered seizure-free, four patients (19%) had >95% reduction in seizures, and two patients (10%) had an 80–94% reduction in seizures. A seizure-free outcome was associated with shorter duration of epilepsy ( P = 0.02). Conclusion – Adult patients with FCD may be candidates for surgical treatment of intractable partial epilepsy. Most individuals have neocortical, extrahippocampal seizures and approximately 50% of patients are rendered seizure-free. [ABSTRACT FROM AUTHOR]
Copyright of Acta Neurologica Scandinavica is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Surgical outcome and predictive factors in adult patients with intractable epilepsy and focal cortical dysplasia.
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  Data: <searchLink fieldCode="JN" term="%22Acta+Neurologica+Scandinavica%22">Acta Neurologica Scandinavica</searchLink>. Feb2006, Vol. 113 Issue 2, p65-71. 7p. 2 Charts, 3 Graphs.
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  Data: <searchLink fieldCode="DE" term="%22Epilepsy%22">Epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22Brain+diseases%22">Brain diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Dysplasia%22">Dysplasia</searchLink><br /><searchLink fieldCode="DE" term="%22Temporal+lobe%22">Temporal lobe</searchLink><br /><searchLink fieldCode="DE" term="%22Cerebral+cortex%22">Cerebral cortex</searchLink>
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  Data: Objectives – To determine the surgical outcome and prognostic factors in adult patients with intractable epilepsy and focal cortical dysplasia (FCD). Materials and methods – We retrospectively studied the operative outcome in 21 consecutive adult patients with FCD who underwent surgical treatment for intractable partial epilepsy. Results – The mean age at surgery was 32.7 years (range, 18–58 years). The median post-operative follow-up was 2.5 years. The FCD was extratemporal in 11 patients, involved the temporal lobe in 10 patients, and was multilobar in eight patients. Eleven patients (52%) were rendered seizure-free, four patients (19%) had >95% reduction in seizures, and two patients (10%) had an 80–94% reduction in seizures. A seizure-free outcome was associated with shorter duration of epilepsy ( P = 0.02). Conclusion – Adult patients with FCD may be candidates for surgical treatment of intractable partial epilepsy. Most individuals have neocortical, extrahippocampal seizures and approximately 50% of patients are rendered seizure-free. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Acta Neurologica Scandinavica is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1111/j.1600-0404.2005.00548.x
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        Text: English
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        Type: general
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      – SubjectFull: Dysplasia
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              Text: Feb2006
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