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下丘脑错构瘤致痴笑发作的急诊切除术后长期疗效。

Long-term outcome after emergency resection of hypothalamic hamartomas for status gelasticus.

机构信息

Divisions of Neurology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona 85013, USA.

出版信息

Neurosurg Focus. 2011 Feb;30(2):E5. doi: 10.3171/2010.12.FOCUS10249.

Abstract

OBJECT

Gelastic seizures are epileptic events characterized by bouts of laughter. They are rare and mostly associated with hypothalamic hamartomas (HHs). Status gelasticus, a rare form of status epilepticus, is defined as a prolonged cluster of gelastic seizures (> 20-30 minutes) without necessarily involving loss of awareness between seizures. Emergency resection of the hamartoma is highly effective in these situations and should be considered as early as possible. The authors retrospectively reviewed their surgical cases to document the success, complications, and long-term follow-up after emergency resection of HHs for status gelasticus.

METHODS

The authors report on a retrospective case series from a single tertiary care center. Three patients who presented with status gelasticus underwent emergency resection of HHs. Demographic details, seizure history, medical treatment, and postoperative follow-up data were evaluated. Long-term follow-up (minimum 2 years) data were obtained either from the last clinic visit notes or via telephone and e-mail contacts. The institutional review board at St. Joseph's Hospital approved this study.

RESULTS

In the last 7 years, of 157 patients who underwent HH resection, the resection was performed on an emergency basis for status gelasticus in 3 cases. At emergency surgery, these 3 patients ranged in age from 9 months to 3.5 years. All of the patients were boys. Delalande and Fohlen Type II, III, and IV lesions were present in the 3 patients. Surgical approaches for resection of HH included an orbitozygomatic, transcallosal anterior interforniceal approach and endoscopic resection. Status gelasticus was terminated following emergency surgery in all cases, and 1 patient was seizure free. Postsurgical complications included, in 1 case, a small right thalamic infarct with mild transient left hemiparesis, which completely resolved within 2 days. Within 2 years of their original surgery, 2 patients underwent further elective surgeries (endoscopic resection and radiosurgery for persistent symptomatic seizures). Follow-up since their most recent surgery ranged from 8 months to 2 years. Two patients were seizure free and 1 patient had greater than 50% reduction in seizures.

CONCLUSIONS

Status gelasticus associated with HHs can be successfully terminated by emergency resection of the HH. Long-term follow-up in the present series suggests good seizure freedom results or at least greater than 50% reduction in seizures, although repeat operations were necessary.

摘要

目的

发笑性癫痫发作是一种以阵发性大笑为特征的癫痫事件。它们很少见,主要与下丘脑错构瘤(HH)有关。作为一种罕见的癫痫持续状态,持续发笑性癫痫持续状态定义为长时间的阵发性发笑发作(> 20-30 分钟),发作之间不一定有意识丧失。在这种情况下,高度有效的紧急切除错构瘤应尽早考虑。作者回顾性审查了他们的手术病例,以记录紧急切除 HH 治疗发笑性癫痫持续状态的成功率、并发症和长期随访结果。

方法

作者报告了来自单一三级护理中心的回顾性病例系列。3 名出现发笑性癫痫持续状态的患者接受了 HH 的紧急切除术。评估了人口统计学细节、癫痫发作史、药物治疗和术后随访数据。通过最近的诊所就诊记录或通过电话和电子邮件联系获得长期随访(至少 2 年)数据。圣约瑟夫医院的机构审查委员会批准了这项研究。

结果

在过去 7 年中,在 157 例接受 HH 切除术的患者中,有 3 例因发笑性癫痫持续状态而紧急进行了手术。在紧急手术中,这 3 名患者的年龄从 9 个月到 3.5 岁不等。所有患者均为男性。Delalande 和 Fohlen Ⅱ型、Ⅲ型和Ⅳ型病变存在于这 3 例患者中。HH 切除术的手术入路包括眶颧、经胼胝体前连合间入路和内镜切除。所有病例均在紧急手术后终止发笑性癫痫持续状态,1 例患者无癫痫发作。术后并发症包括 1 例右侧丘脑小梗死伴轻度短暂性左侧偏瘫,2 天内完全缓解。在原始手术后 2 年内,2 例患者接受了进一步的择期手术(内镜切除和放射外科治疗持续性有症状的癫痫发作)。自最近一次手术后的随访时间为 8 个月至 2 年。2 例患者无癫痫发作,1 例患者癫痫发作减少> 50%。

结论

HH 相关的发笑性癫痫持续状态可以通过紧急切除 HH 成功终止。本系列的长期随访结果表明,癫痫发作完全缓解或至少减少> 50%,尽管需要重复手术。

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