Pediatric meningioma and seizures: A scoping review.

IF 1.2
Emma Ye, Ashwin Gupta, Alexander T Lyons, Shilpa B Reddy, Devang J Pastakia, Michael C Dewan
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Abstract

Objective: Pediatric meningiomas (PM) are rare tumors with unique clinical characteristics, including their association with seizures. This review aims to explore the available evidence regarding the nature of this association, the types of evidence available, and the gaps in our understanding.

Methods: We synthesized evidence from systemic literature search. We identified key clinical concepts including the frequency of seizures as a presenting feature, seizure outcomes following surgical treatment, the relationship between extent of resection and seizure freedom, the impact of histologic features or grade on seizure freedom, and the role of post-operative anti-seizure medications (ASMs). Two proportion z-tests were performed with a p < 0.05 significance threshold.

Results: In our search, we found 824 pediatric meningioma cases, with 293 (35.6%) presenting with seizure(s) at the time of meningioma diagnosis. Varying information regarding tumor grade, recurrence, seizure outcomes, and use of ASM was available in all 293 patients. One hundred-thirteen cases had a listed meningioma grade, with 80 (70.8%) classified as grade I, 19 (16.8%) as grade II, and 14 (12.4%) as grade III. 12 of the 113 patients with graded tumors (10.6%) received post-operative ASMs. Post-operative seizure status was reported in 76 of these patients and 50 (65.8%) achieved seizure freedom. Twenty-one underwent subtotal resection and only 2 of 7 (28.6%) were known to have had seizure freedom.

Conclusions: Seizures are a recognized clinical feature in pediatric meningioma, occurring in approximately 36% of patients. They may present at diagnosis or emerge as a postoperative complication, with implications for long-term neurological outcomes. Surgical resection remains the standard of care for pediatric meningioma, and a greater extent of resection improves seizure outcomes. The role of post-resection ASMs and the relationship between seizures and molecular characteristics of pediatric meningioma warrants further investigation.

儿童脑膜瘤和癫痫:范围回顾。
目的:小儿脑膜瘤(PM)是一种罕见的肿瘤,具有独特的临床特征,包括与癫痫发作有关。本综述旨在探讨有关这种关联的性质的现有证据,现有证据的类型以及我们在理解上的差距。方法:通过系统文献检索,综合证据。我们确定了关键的临床概念,包括作为表现特征的癫痫发作频率,手术治疗后的癫痫发作结果,切除程度与癫痫发作自由之间的关系,组织学特征或分级对癫痫发作自由的影响,以及术后抗癫痫药物(asm)的作用。结果:在我们的搜索中,我们发现了824例儿童脑膜瘤病例,其中293例(35.6%)在脑膜瘤诊断时出现癫痫发作。在所有293例患者中,关于肿瘤分级、复发、癫痫发作结局和ASM使用的不同信息均可获得。113例脑膜瘤分级,其中ⅰ级80例(70.8%),ⅱ级19例(16.8%),ⅲ级14例(12.4%)。113例分级肿瘤患者中有12例(10.6%)术后接受了asm治疗。76例患者报告了术后癫痫发作情况,其中50例(65.8%)实现了癫痫发作自由。21例行次全切除,7例中仅有2例(28.6%)癫痫发作自由。结论:癫痫发作是儿童脑膜瘤的一个公认的临床特征,发生在大约36%的患者中。它们可能在诊断时出现,也可能作为术后并发症出现,对神经系统的长期预后有影响。手术切除仍然是儿童脑膜瘤的标准治疗方法,更大程度的切除可以改善癫痫发作的结果。小儿脑膜瘤的分子特征与癫痫发作的关系及术后asm的作用值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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