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切除神经节神经胶质瘤后的长期癫痫控制结果。

Long-term seizure control outcomes after resection of gangliogliomas.

机构信息

Northern California Comprehensive Epilepsy Center, Brain Tumor Research Center, and Department of Neurological Surgery, University of California, San Francisco, California 94143, USA.

出版信息

Neurosurgery. 2012 Jun;70(6):1406-13; discussion 1413-4. doi: 10.1227/NEU.0b013e3182500a4c.

Abstract

BACKGROUND

Gangliogliomas are rare glioneuronal tumors that typically cause refractory seizures during the first 3 decades of life.

OBJECTIVE

To determine the prognosticators of seizure outcome after surgery for ganglioglioma.

METHODS

We reviewed the cases of 66 patients who underwent resection of gangliogliomas at the University of California, San Francisco. Demographic, seizure history, and operative data were examined for statistical association with postoperative seizure outcomes.

RESULTS

Of the 66 patients who underwent surgical resection of ganglioglioma, 49 patients (74%) presented with a history of seizures. Of those 49 patients, 50% presented with intractable epilepsy. Temporal lobe gangliogliomas were present in 76% of the patients who presented with a history of seizures. Electrocorticography was performed on 35% of the patients, and of those patients, 82% underwent extended lesionectomy to remove abnormally epileptogenic extralesional tissue. The median follow-up duration was 6.9 years, during which tumor progression occurred in 38% of patients who underwent subtotal resection and in 8% of patients who underwent gross total resection (P = .02). Overall, 85% of patients were seizure free (International League Against Epilepsy class I or II) 5 years after surgery. Subtotal resection was associated with poor seizure outcomes 1 year after resection (odds ratio = 14.6; 95% confidence interval = 2.4-87.7): rates of seizure freedom were 54% after subtotal resection, 96% after gross total resection, and 93% after gross total resection with intraoperative electrocorticography-guided extended lesionectomy.

CONCLUSION

We report excellent long-term seizure control outcomes after surgery for gangliogliomas. Intraoperative electrocorticography may be a useful adjunct for guiding extended resection in certain pharmacoresistant epilepsy patients with gangliogliomas. Subtotal resection is associated with higher rates of tumor progression and nonoptimal seizure outcomes.

摘要

背景

神经节神经胶质瘤是一种罕见的胶质神经元肿瘤,通常在生命的头 30 年内引起难治性癫痫发作。

目的

确定神经节神经胶质瘤手术后癫痫发作结果的预测因素。

方法

我们回顾了在加利福尼亚大学旧金山分校接受神经节神经胶质瘤切除术的 66 例患者的病例。检查了人口统计学、癫痫发作史和手术数据,以确定与术后癫痫发作结果的统计学关联。

结果

在接受神经节神经胶质瘤手术切除的 66 例患者中,有 49 例(74%)有癫痫发作史。在这 49 例患者中,50%的患者患有难治性癫痫。有癫痫发作史的患者中,76%的患者存在颞叶神经节神经胶质瘤。35%的患者进行了皮层脑电图检查,其中 82%的患者进行了扩大病变切除术以切除异常致痫性的瘤外组织。中位随访时间为 6.9 年,次全切除术后有 38%的患者肿瘤进展,而全切除术后有 8%的患者肿瘤进展(P=0.02)。总的来说,85%的患者在手术后 5 年内无癫痫发作(国际抗癫痫联盟 I 级或 II 级)。次全切除术后 1 年癫痫发作结果较差(优势比=14.6;95%置信区间=2.4-87.7):次全切除后癫痫无发作率为 54%,全切除后为 96%,全切除后联合术中皮层脑电图引导扩大病变切除术为 93%。

结论

我们报告了神经节神经胶质瘤手术后长期癫痫控制效果良好。术中皮层脑电图可能是指导某些耐药性癫痫伴神经节神经胶质瘤患者扩大切除的有用辅助手段。次全切除与更高的肿瘤进展率和不理想的癫痫发作结果相关。

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