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Surgery for focal cortical dysplasia in children using intraoperative mapping

Terra, Vera C. ; Thomé, Ursula ; Rosset, Sara S. ; Funayama, Sandra S. ; dos Santos, Antonio Carlos ; dos Santos, Marcelo Volpon ; Sakamoto, Américo C. ; Machado, Helio R.

Child's nervous system, 2014-11, Vol.30 (11), p.1839-1851 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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Título:
Surgery for focal cortical dysplasia in children using intraoperative mapping
Autor: Terra, Vera C. ; Thomé, Ursula ; Rosset, Sara S. ; Funayama, Sandra S. ; dos Santos, Antonio Carlos ; dos Santos, Marcelo Volpon ; Sakamoto, Américo C. ; Machado, Helio R.
Assuntos: Adolescent ; Brain Mapping ; Brain Waves - physiology ; Chi-Square Distribution ; Child ; Electroencephalography ; Epilepsy - complications ; Epilepsy - surgery ; Female ; Follow-Up Studies ; Humans ; Intraoperative Neurophysiological Monitoring - methods ; Male ; Malformations of Cortical Development - classification ; Malformations of Cortical Development - complications ; Malformations of Cortical Development - surgery ; Medicine ; Medicine & Public Health ; Neurosciences ; Neurosurgery ; Neurosurgery - methods ; Retrospective Studies ; Special Annual Issue
É parte de: Child's nervous system, 2014-11, Vol.30 (11), p.1839-1851
Notas: ObjectType-Article-2
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Descrição: Objective Children with malformation of cortical development represent a significant proportion of pediatric epilepsy surgery candidates. Here, we describe a single-center experience with pediatric patients who underwent surgery for intractable epilepsy due to focal cortical dysplasia (FCD). Methods Clinical data of 78 patients under 18 years of age with diagnosis of intractable epilepsy due to FCD who underwent surgery from January 1996 to January 2012 were reviewed comparing data of patients submitted to electrocorticography (ECoG) with those without ECoG. Results Patients’ mean age at surgery was 8.52 ± 4.99 years; mean age at epilepsy onset was 2.55 ± 3.01 years. Almost 80 % of the patients underwent ECoG register that was essential for delimitation of surgical resection in 66 out of 78 patients. ECoG was performed in all patients with extratemporal lesions, and the most common FCD found was type II. Seizure outcome was similar in groups with or without ECoG. Conclusions Tailored resection of FCD lesions for intractable epilepsy can be safely performed in children with a good seizure outcome and low complication rate. Epilepsy surgery should be considered for all patients with FCD and refractory epilepsy.
Editor: Berlin/Heidelberg: Springer Berlin Heidelberg
Idioma: Inglês

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Surgery for focal cortical dysplasia in children using intraoperative mapping

Terra, Vera C. ; Thomé, Ursula ; Rosset, Sara S. ; Funayama, Sandra S. ; dos Santos, Antonio Carlos ; dos Santos, Marcelo Volpon ; Sakamoto, Américo C. ; Machado, Helio R.

Berlin/Heidelberg: Springer Berlin Heidelberg

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