neuro-oncology surgery

  • 文章类型: Case Reports
    儿童巨大的幕上脑肿瘤(GSBT)是小儿神经外科手术中罕见且极具挑战性的实体。诸如年轻患者年龄等因素,需要紧急干预,术中失血,和持续升高的颅内压症状是所面临的困难的例子。最近,关于成人神经外科增强现实(AR)的文献越来越多。相比之下,AR在小儿神经外科手术中的应用相对较少。尽管如此,我们假设AR系统将有助于理解复杂GSBT解剖结构的空间关系,以便及时进行术前规划。这项研究描述了我们在将AR作为三例小儿GSBT的潜在工具进行试验方面的经验。总的来说,AR平台为我们的神经外科团队提供了出色的术前决策视觉空间见解。然而,我们观察到,在神经外科团队讨论每个临床病例之前,需要大量时间来建立AR系统.与现有文献一致,我们的初步研究结果显示,在这些对时间敏感的儿童脑肿瘤的临床工作流程中无缝实施该技术之前,仍有一些障碍需要解决.据我们所知,这是第一项报道AR用于复杂儿科GSBT病例的潜在用途的研究.
    Giant supratentorial brain tumors (GSBTs) in children are uncommon and extremely challenging entities unique to pediatric neurosurgery. Factors such as young patient age, need for urgent intervention, intraoperative blood loss, and ongoing raised intracranial pressure symptoms are examples of difficulties faced. Recently, there has been a growing body of literature on augmented reality (AR) in adult neurosurgery. In contrast, the use of AR in pediatric neurosurgery is comparatively less. Nonetheless, we postulate that AR systems will be helpful for understanding spatial relationships of complex GSBT anatomy for preoperative planning in a timely fashion. This study describes our experience in trialing AR as a potential tool for three cases of pediatric GSBTs. Overall, the AR platform offers our neurosurgical team excellent visuospatial insights for preoperative decision-making. However, we observe that substantial time is required to set up the AR system prior to each clinical case discussion by the neurosurgical team. In congruency with existing literature, our preliminary results report that there are still obstacles that need to be addressed before the technology can be seamlessly implemented into the clinical workflow for these time-sensitive childhood brain tumors. To our knowledge, this is the first study to report the potential use of AR for complex pediatric GSBT cases.
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  • 文章类型: Journal Article
    室管膜瘤是从脑实质中发现的室管膜细胞发展而来的神经上皮肿瘤,可以扩散到脊髓的任何部分。影响中枢神经系统(CNS)的所有恶性肿瘤中有3%至6%是室管膜瘤。即使是最有才华的外科医生也受到脊髓室管膜瘤的挑战;结果,应该继续研究这种临床现象。自1979年以来,世界卫生组织(WHO)发布了中枢神经系统恶性肿瘤的分类和分级系统,以确保全球范围内一致的诊断标准。世界卫生组织准备了关于这些肿瘤的最新资料,特别注意分子技术,以更高的准确性和清晰度对每位患者的治疗管理进行分类。我们彻底回顾了流行病学的文献,病因学,诊断,以及脊髓室管膜瘤的治疗,因为最近还没有对这些肿瘤进行审查。这包括对2021年WHO中枢神经系统肿瘤分类的修改。
    Ependymomas are neuroepithelial tumors that develop from ependymal cells found in the brain parenchyma and can spread to any part of the spinal cord. Three to six percent of all malignancies affecting the central nervous system (CNS) are ependymomas. Even the most talented surgeons are challenged by spinal cord ependymomas; as a result, research into this clinical phenomenon should continue. Since 1979, the World Health Organization (WHO) has published a classification and grading system for CNS malignancies to ensure consistent diagnostic standards worldwide. The WHO prepared an update on these tumors, paying particular attention to molecular techniques to categorize the therapeutic management of each patient with greater accuracy and clarity. We thoroughly reviewed the literature on the epidemiology, etiology, diagnosis, and treatment of spinal ependymomas since there has not been a recent review of these tumors. This included modifications to the 2021 WHO Classification of Tumors of the Central Nervous System.
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  • 文章类型: Journal Article
    UNASSIGNED:清醒开颅手术与多模态神经生理标测和轴内肿瘤切除监测的结合没有得到很好的描述,但可能有我们试图调查的理论上的好处。
    UNASSIGNED:所有接受清醒开颅手术切除肿瘤的患者,皮质和/或皮质下刺激以及一个或多个皮质脑电图(ECoG/EEG),从两个中心的两名外科医生在5年内的手术记录中确定了运动或体感诱发电位。病人,对手术和结局数据进行了整理.进行统计分析以评估预测术中癫痫发作和手术结果的因素。
    未经批准:83例患者的中位年龄为50岁(18-80岁)。80%的胶质瘤(37%的低级别)和13%的转移。35%(语言区域)和24%(运动区域)的皮质作图为阴性。80%的患者实现了完全或几乎完全切除,5%的严重长期神经功能缺损。负皮质作图与正皮质下作图相结合的比例为42%,与接受正皮质作图的患者相比,切除率的程度无显着差异(p=0.95)。在14%内无法完成唤醒映射,但对切除程度(p=0.55)或并发症发生率(p=0.09)没有影响。术中癫痫发作发生率为11%,与术中EEG尖峰显着相关(p=0.003)。
    UNASSIGNED:Awake多模态监测是一种安全且耐受性良好的技术。在清醒开颅手术中止的情况下,它可以保留切除程度和临床结果。负皮质映射结合正皮质下映射也被证明是安全的,虽然迄今没有很好的描述。皮质脑电图进一步能够区分癫痫发作活动和真正的阳性映射,以及在完全临床癫痫发作之前成功治疗尖峰。
    UNASSIGNED: The combination of awake craniotomy with multimodal neurophysiological mapping and monitoring in intra-axial tumour resection is not well described, but may have theoretical benefits which we sought to investigate.
    UNASSIGNED: All patients undergoing awake craniotomy for tumour resection with cortical and/or subcortical stimulation together with one or more of electrocorticography (ECoG/EEG), motor or somatosensory evoked potentials were identified from the operative records of two surgeons at two centres over a 5 year period. Patient, operative and outcome data were collated. Statistical analysis was performed to evaluate factors predictive of intra-operative seizures and surgical outcomes.
    UNASSIGNED: 83 patients with a median age 50 years (18-80 years) were included. 80% had gliomas (37% low grade) and 13% metastases. Cortical mapping was negative in 35% (language areas) and 24% (motor areas). Complete or near total resection was achieved in 80% with 5% severe long-term neurological deficits. Negative cortical mapping was combined with positive subcortical mapping in 42% with no significant difference in extent of resection rates to patients undergoing positive cortical mapping (p = 0.95). Awake mapping could not be completed in 14%, but with no compromise to extent of resection (p = 0.55) or complication rates (p = 0.09). Intraoperative seizures occurred in 11% and were significantly associated with intra-operative EEG spikes (p = 0.003).
    UNASSIGNED: Awake multi-modal monitoring is a safe and well tolerated technique. It provides preservation of extent of resection and clinical outcomes in cases of aborted awake craniotomy. Negative cortical mapping in combination with positive subcortical mapping was also shown to be safe, although not hitherto well described. Electrocorticography further enables the differentiation of seizure activity from true positive mapping, and the successful treatment of spikes prior to full clinical seizures occurring.
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