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Surgical Management of Pediatric Tumor-Associated Epilepsy

Neurosurgery Service, Walter Reed Army Medical Center, Washington, DC, Uniformed Services University of the Health Sciences, Bethesda, MD

Youssef G. Comair, MD

Division of Neurosurgery, American University of Beirut Medical Center, Beirut, Lebanon

Elaine Wyllie, MD

Department of Neurology, The Cleveland Clinic Foundation, Cleveland, OH

Joann Palmer, RN

Department of Neurosurgery, The Cleveland Clinic Foundation, Cleveland, OH

Harold H. Morris, MD

Department of Neurology, The Cleveland Clinic Foundation, Cleveland, OH

Joseph F. Hahn, MD

Department of Neurosurgery, The Cleveland Clinic Foundation, Cleveland, OH

Brain tumors are a common cause of seizures in children. Early surgical treatment can improve seizure outcome, but controversy exists regarding the most appropriate type of surgical intervention. Some studies suggest tumor resection alone is sufficient, while others recommend mapping and resection of the surrounding epileptogenic foci to optimize seizure outcome. To address this issue, we reviewed the charts of 34 pediatric patients aged 18 months to 20 years with medically intractable epilepsy and primary brain tumors. The average age at operation was 12.6 years, and patients had seizures for an average of 6.4 years. The majority of tumors were located in the temporal lobe. Seventeen patients, because of tumor location near an eloquent area, underwent extraoperative mapping using subdural electrode grids prior to definitive tumor resection. Fourteen of these patients had a gross total tumor resection, yet only two had a distinct zone of ictal onset identified and resected. The remaining 17 patients had tumors either in the nondominant hemisphere or far removed from speech-sensitive areas, and therefore did not undergo extraoperative subdural electroencephalograph mapping. Fourteen of these patients also had a gross total tumor resection, while none had intraoperative electrocorticography to guide the resection of additional nontumoral tissue. Overall, of the 28 patients treated with a gross total tumor resection, 24 (86%) are seizure free, while the other four are significantly improved. Of the six patients who had a subtotal tumor removal, five have persistent seizures. The mean follow-up was 3.6 years. We conclude that in children and adolescents, completeness of tumor resection is the most important factor in determining seizure outcome. The routine mapping and resection of epileptogenic foci might not be necessary in the majority of patients. As a corollary, the use of subdural electrode grids in pediatric patients with tumor-associated epilepsy should be limited to cases requiring extraoperative cortical stimulation for localization of nearby eloquent cortex. (J Child Neurol 1999;14:15-25).

Journal of Child Neurology, Vol. 14, No. 1, 15-25 (1999)
DOI: 10.1177/088307389901400102


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