Electrical stimulation mapping guides individualized surgical approach in an epilepsy-associated tumor within language representing cortex

IF 1.9 4区 医学 Q3 CLINICAL NEUROLOGY
Susana Palao-Duarte, Dirk-Matthias Altenmüller, Christian Scheiwe, Anika Schinkel, Hansjörg Mast, Horst Urbach, Theo Demerath, Marius Schwabenland, Andreas Schulze-Bonhage, Kathrin Wagner, Marcel Heers
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After non-invasive presurgical diagnostics, we performed an invasive subdural electroencephalogram (iEEG) with extraoperative electrical stimulation mapping (ESM) prior to tumor surgery.<span><sup>2</sup></span></p><p>A 22-year-old female university student with left-sided temporal lobe epilepsy was referred for invasive video-EEG monitoring and language mapping to guide resective tumor surgery. Her epilepsy began at the age of 20 years, and it was characterized by focal aware seizures with speech arrest, occasionally followed by focal impaired awareness seizures. Under monotherapy with Levetiracetam up to 4 g/day, she had two to three focal aware seizures/day, despite which she was able to finish her university studies. High-resolution 3T structural magnetic resonance imaging (s-MRI) showed a slowly progressive, partially contrast-enhancing low-grade neuroglial tumor located at the left posterior superior temporal gyrus (Figure 1, Panels A and B) and the basal insula. A functional language MRI (l-fMRI) confirmed left-hemispheric language dominance with activations directly adjacent to the tumor (Figure 1, Panel C). Presurgical neuropsychological assessment (NPS) revealed discrete word-finding difficulties, partly reduced verbal fluency and impaired verbal short-term and working memory performance. The right-handed patient had a normal physical examination. Written informed consent was obtained for the scientific publication of the patient's clinical data.</p><p>Invasive video-EEG monitoring for 4 days with a 32-contact subdural grid implanted over the left temporal lobe was performed (Figure 1, Panel D). The ESM language cortical mapping with 50 Hz (biphasic pulses, duration 250 μs, bipolar stimulation up to 15 mA, referential stimulation up to 18 mA) comprised six different language tasks as described in detail before.<span><sup>3</sup></span> Language representations were identified in contacts B2-3, B6, C5-C8, and D7 (Figure 1, Panel D). The language representation around contacts A3-4 and B4-5 could not be assessed due to unavoidable afterdischarges despite the additional use of lorazepam. In summary, the ESM showed a clear overlap of language representation and tumor in the left superior temporal gyrus. The irritative zone and the seizure onset zone overlapped with language representations (Figure 1, Panel D).</p><p>Due to the tumor's location, only the contrast-enhancing solid component and the cyst membrane could be resected via a transsylvian approach to minimize the risk of postoperative language deficits. No need for awake surgery with additional intraoperative language mapping was seen. The postsurgical NPS revealed unchanged performance, especially in language-related tasks, and no deterioration was found. 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引用次数: 0

Abstract

In epilepsy patients with tumors involving the cortex with language representations, a comprehensive interdisciplinary workup is required to protect language function during surgical resection.1

We report the presurgical evaluation of a patient with focal epilepsy due to a progressive tumor in the language area of the left temporal lobe. After non-invasive presurgical diagnostics, we performed an invasive subdural electroencephalogram (iEEG) with extraoperative electrical stimulation mapping (ESM) prior to tumor surgery.2

A 22-year-old female university student with left-sided temporal lobe epilepsy was referred for invasive video-EEG monitoring and language mapping to guide resective tumor surgery. Her epilepsy began at the age of 20 years, and it was characterized by focal aware seizures with speech arrest, occasionally followed by focal impaired awareness seizures. Under monotherapy with Levetiracetam up to 4 g/day, she had two to three focal aware seizures/day, despite which she was able to finish her university studies. High-resolution 3T structural magnetic resonance imaging (s-MRI) showed a slowly progressive, partially contrast-enhancing low-grade neuroglial tumor located at the left posterior superior temporal gyrus (Figure 1, Panels A and B) and the basal insula. A functional language MRI (l-fMRI) confirmed left-hemispheric language dominance with activations directly adjacent to the tumor (Figure 1, Panel C). Presurgical neuropsychological assessment (NPS) revealed discrete word-finding difficulties, partly reduced verbal fluency and impaired verbal short-term and working memory performance. The right-handed patient had a normal physical examination. Written informed consent was obtained for the scientific publication of the patient's clinical data.

Invasive video-EEG monitoring for 4 days with a 32-contact subdural grid implanted over the left temporal lobe was performed (Figure 1, Panel D). The ESM language cortical mapping with 50 Hz (biphasic pulses, duration 250 μs, bipolar stimulation up to 15 mA, referential stimulation up to 18 mA) comprised six different language tasks as described in detail before.3 Language representations were identified in contacts B2-3, B6, C5-C8, and D7 (Figure 1, Panel D). The language representation around contacts A3-4 and B4-5 could not be assessed due to unavoidable afterdischarges despite the additional use of lorazepam. In summary, the ESM showed a clear overlap of language representation and tumor in the left superior temporal gyrus. The irritative zone and the seizure onset zone overlapped with language representations (Figure 1, Panel D).

Due to the tumor's location, only the contrast-enhancing solid component and the cyst membrane could be resected via a transsylvian approach to minimize the risk of postoperative language deficits. No need for awake surgery with additional intraoperative language mapping was seen. The postsurgical NPS revealed unchanged performance, especially in language-related tasks, and no deterioration was found. The neuropathological diagnosis was a low-grade neuroepithelial tumor not elsewhere classified (IDH1, IDH2: wild-type; Multiplex Ligation-Dependent Probe Amplification: no BRAF-V600e mutation or BRAF-KIAA1549-fusion or homozygous CDKN2A/B loss, 850 k methylome analysis inconclusive). Postsurgical s-MRI showed no complications (Figure 1F). As it was impossible to resect the entire tumor and the seizure onset zone, it is likely that the patient will not become seizure-free after surgery.

The case presented illustrates how individualized concepts guide surgical decisions in patients with focal epilepsy due to a tumor in eloquent areas. The aim of removing the most relevant, contrast-enhancing tumor part was achieved without endangering cortical language representations based on solid ESM findings. It was necessary to prioritize avoiding damage to language areas over the complete removal of the tumor and the seizure onset area.

Robust functional assessment of language representations is critical to minimize the risk of permanent postoperative language deficits. The ESM is the gold standard method for accurately delineating the language-relevant cortex, although the procedure is not yet standardized.2-4 As described by Wellmer et al., the type and number of applied language tasks vary between centers.3 The l-fMRI allows visualization of hemispheric lateralization of language, but its localization value is not accurate enough to define the margins of surgical resection.4-6 For a more rigorous evaluation before and after surgery, NPS assessment of language-associated functions is indispensable.7

The evaluation of functional connectivity in iEEG is promising but has not yet been proven to be as accurate as ESM in iEEG.8 Also, awake tumor surgery does not offer similar flexibility in choosing time windows free of afterdischarges and multimodal language tasks for comprehensive language mappings. So, ESM in iEEG remains the gold standard for guiding neurosurgical resection adjacent to cortical language representations.

Abstract Image

电刺激图引导语言代表皮层癫痫相关肿瘤的个体化手术方法。
1 我们报告了对一名因左颞叶语言区进展性肿瘤而患局灶性癫痫的患者进行的术前评估。2A 22 岁的女大学生患有左侧颞叶癫痫,她被转诊接受有创视频脑电图监测和语言图谱检查,以指导肿瘤切除手术。她的癫痫始于 20 岁,主要表现为局灶性意识发作伴言语停止,偶尔伴有局灶性意识障碍发作。在使用左乙拉西坦(Levetiracetam)单药治疗(最高4克/天)的情况下,她每天有2到3次局灶性意识发作,尽管如此,她仍能完成大学学业。高分辨率3T结构磁共振成像(s-MRI)显示,左侧颞上回后部(图1,面板A和B)和岛叶基底有一个缓慢进展、部分对比度增强的低级别神经胶质瘤。功能性语言核磁共振成像(l-fMRI)证实了左侧大脑半球的语言优势,其激活直接邻近肿瘤(图 1,C 组)。手术前的神经心理学评估(NPS)显示,患者存在离散性词汇查找困难、部分言语流畅性降低、言语短期记忆和工作记忆能力受损。这名右撇子患者的体格检查结果正常。在左侧颞叶上植入了一个32触点硬膜下网格,进行了为期4天的有创视频-EEG监测(图1,D组)。ESM语言皮层图谱以50赫兹(双相脉冲,持续时间250微秒,双极刺激达15毫安,参考刺激达18毫安)绘制,包括六种不同的语言任务,详见之前的描述。尽管额外使用了劳拉西泮,但由于不可避免的后放电,触点 A3-4 和 B4-5 周围的语言表达仍无法评估。总之,ESM 显示左侧颞上回的语言表达与肿瘤明显重叠。刺激区和癫痫发作区与语言表达重叠(图 1,D 组)。由于肿瘤的位置,只能通过经颞侧入路切除对比度增强的实性成分和囊膜,以尽量减少术后语言障碍的风险。无需进行清醒手术和额外的术中语言映射。手术后的 NPS 显示,患者的表现没有变化,尤其是在与语言相关的任务中,没有发现任何恶化。神经病理学诊断为未在别处分类的低级别神经上皮性肿瘤(IDH1、IDH2:野生型;多重连接依赖性探针扩增:无 BRAF-V600e 突变或 BRAF-KIAA1549 融合或同种 CDKN2A/B 缺失,850 k 甲基组分析未确定)。手术后的 s-MRI 显示无并发症(图 1F)。由于不可能切除整个肿瘤和癫痫发作区,因此患者术后很可能无法摆脱癫痫发作。根据可靠的 ESM 研究结果,在不危及大脑皮层语言表达的情况下,实现了切除最相关的、对比度增强的肿瘤部分的目标。与完全切除肿瘤和癫痫发作区相比,有必要优先考虑避免对语言区造成损害。2-4 正如 Wellmer 等人所描述的那样,不同中心应用的语言任务类型和数量各不相同。3 l-fMRI 可以显示语言的半球侧化,但其定位价值还不足以准确界定手术切除的边缘。7 iEEG 中的功能连接评估很有前景,但尚未被证明与 iEEG 中的 ESM 一样准确。8 此外,清醒肿瘤手术在选择无放电后时间窗和多模态语言任务以进行全面语言映射方面不具备类似的灵活性。 因此,iEEG 中的 ESM 仍是指导邻近皮层语言表征的神经外科切除术的黄金标准。
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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来源期刊
Epileptic Disorders
Epileptic Disorders 医学-临床神经学
CiteScore
4.10
自引率
8.70%
发文量
138
审稿时长
6-12 weeks
期刊介绍: Epileptic Disorders is the leading forum where all experts and medical studentswho wish to improve their understanding of epilepsy and related disorders can share practical experiences surrounding diagnosis and care, natural history, and management of seizures. Epileptic Disorders is the official E-journal of the International League Against Epilepsy for educational communication. As the journal celebrates its 20th anniversary, it will now be available only as an online version. Its mission is to create educational links between epileptologists and other health professionals in clinical practice and scientists or physicians in research-based institutions. This change is accompanied by an increase in the number of issues per year, from 4 to 6, to ensure regular diffusion of recently published material (high quality Review and Seminar in Epileptology papers; Original Research articles or Case reports of educational value; MultiMedia Teaching Material), to serve the global medical community that cares for those affected by epilepsy.
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