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结节性硬化症患儿的侧裂周围皮层致痫灶切除术:结节中是否含有功能?

Do tubers contain function? Resection of epileptogenic foci in perirolandic cortex in children with tuberous sclerosis complex.

机构信息

Department of Neurosurgery, New York University School of Medicine, New York, New York, USA.

出版信息

Epilepsia. 2010 Jul;51(7):1242-51. doi: 10.1111/j.1528-1167.2009.02493.x. Epub 2010 May 17.

Abstract

PURPOSE

Surgical resection of single, dominant, epileptogenic lesions in patients with tuberous sclerosis complex (TSC) is now accepted as an effective therapy. However, patients with symptomatic tubers in eloquent cortex are sometimes not offered surgery because of the concern for postoperative neurologic morbidity. In this study, we examine our results in children undergoing surgery for resection of tubers and associated seizure foci in rolandic and perirolandic cortex.

METHODS

Between 1998 and 2008, 52 pediatric patients (mean age 4 years) with TSC underwent epilepsy surgery at the NYU Comprehensive Epilepsy Center. Fifteen of these patients underwent multistage surgery for invasive mapping of seizure foci and surrounding functional cortex followed by resection of tubers/seizure foci in or near rolandic cortex. Data were retrospectively collected and neurologic outcomes were tabulated.

RESULTS

Postoperatively, four patients (27%) had either new hemiparesis or worsening of a preexisting hemiparesis. However, all patients were back to their neurologic baselines at 3-month follow-up, yielding no permanent postoperative deficits. The modified Engel outcome was class I in nine patients (60%), class II in three patients (20%), class III in two patients (13%), and class IV in one patient (7%) after 40 months mean follow-up.

DISCUSSION

Surgical resection of tubers and associated epileptogenic foci in rolandic and perirolandic cortex in children with TSC is feasible, with low neurologic morbidity, and yields good seizure control. These results suggest that tubers and perituberal epileptogenic foci can be safely resected even in eloquent regions because of reorganization of functional cortex or because these lesions contain no neurologic function.

摘要

目的

目前,对于结节性硬化症(TSC)患者的单个、优势、致痫性病变进行手术切除已被广泛接受,是一种有效的治疗方法。然而,由于担心术后神经功能障碍,一些存在语言皮质内症状性结节的患者并未接受手术治疗。在这项研究中,我们研究了在接受手术切除罗兰氏区和周围脑回的结节和相关致痫灶的 TSC 患儿中的结果。

方法

1998 年至 2008 年间,在纽约大学综合癫痫中心,有 52 名儿科患者(平均年龄 4 岁)接受了癫痫手术。其中 15 名患者接受了多阶段手术,对致痫灶和周围功能皮质进行了侵袭性映射,然后切除了罗兰氏区或附近的结节/致痫灶。回顾性收集数据并列出神经学结果。

结果

术后,4 名患者(27%)出现新发偏瘫或原有偏瘫加重。然而,所有患者在 3 个月随访时均恢复到神经基线水平,没有永久性术后缺陷。改良的恩格尔结局分类为 I 级的有 9 例(60%),II 级的有 3 例(20%),III 级的有 2 例(13%),IV 级的有 1 例(7%),平均随访 40 个月。

讨论

在 TSC 儿童中,对罗兰氏区和周围脑回的结节和相关致痫灶进行切除是可行的,神经并发症发生率低,并且可以很好地控制癫痫发作。这些结果表明,即使在语言区,结节和结节周围的致痫灶也可以安全切除,这是由于功能皮质的重组,或者因为这些病变不包含神经功能。

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