小儿脑室内上皮瘤:人口统计学、临床特征和疗效的系统回顾

Mohammad Faizan Khan, A. Conching, Lane Fry, Dillon Putzer, Ammar Haider, Ali S. Haider, G. Ferini, Mayur Sharma, G. Umana, Paolo Palmisciano, Gina Watanabe
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摘要

背景:室管膜内肿瘤是一种罕见的肿瘤,占所有原发性小儿脑肿瘤的 5 - 7%。小儿脑室内上皮瘤是这些肿瘤中的一个复杂子集,目前的文献对其讨论较少。虽然手术通常是公认的首选治疗方法,但有关临床过程和预后的信息仅限于异质性病例报告和侧重于特定组织学亚型或脑室位置的小型病例系列。我们对小儿脑室内上皮瘤进行了系统性回顾,以调查患者人群、肿瘤特征、管理策略和相关结果。项目方法:根据PRISMA指南检索了PubMed、Scopus、Web-of-Science和Cochrane,纳入了报告室管膜内上胚瘤儿科患者的研究。对临床特征、治疗方案和结果进行了分析。结果:共纳入9项研究,70名患者。大多数患者为男性(54%),确诊时平均年龄为7岁(0.2-17岁),经常出现恶心呕吐(38%)、头痛(31%)和共济失调(25%)。肿瘤主要位于第四脑室(79%),大多数肿瘤为WHO 2级(73%)。肿瘤平均体积为 3 立方厘米(0.1-13.2 厘米)。治疗方法包括手术切除(96%)、放疗(87%)和化疗(38%)。69%的病例实现了大体全切除。颅神经缺损是最常见的术后并发症(71%)。最常见的治疗组合包括手术切除和放射治疗(53%)。这些患者的平均总生存期为 50 个月。结论/影响:小儿脑室内上皮瘤是一种罕见肿瘤,有关治疗策略的信息非常有限。治疗的主要方法是彻底手术切除。与外胚窦瘤相比,室管膜内上胚窦瘤的总体预后似乎较差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraventricular Ependymoma in Pediatric Patients: A Systematic Review of Demographics, Clinical Characteristics, and Outcomes
Background: Intraventricular neoplasms are rare occurrences observed in 5 – 7% of all primary pediatric brain tumors. Pediatric intraventricular ependymomas are a complex subset of these tumors, poorly discussed across the current literature. Although surgery is generally the accepted treatment of choice, information on clinical course and outcomes is limited to heterogeneous case reports and small case series focusing on specific histologic subtypes or ventricular locations. We conducted a systematic review on pediatric intraventricular ependymomas to survey the patient population, tumor characteristics, management strategies, and associated outcomes. Project Methods: PubMed, Scopus, Web-of-Science, and Cochrane were searched upon the PRISMA guidelines to include studies reporting pediatric patients with intraventricular ependymomas. Clinical characteristics, treatment protocols, and outcomes were analyzed. Results: A total of 9 studies with 70 patients were included. Most patients were male (54%), diagnosed at a mean age of 7 years (range, 0.2-17), and frequently exhibited nausea and vomiting (38%), headache (31%), and ataxia (25%). Tumors were predominantly located in the fourth ventricle (79%) and most tumors were WHO grade 2 (73%). Mean tumor volume was 3 cm3 (range, 0.1-13.2). Management included surgical resection (96%), radiotherapy (87%), and chemotherapy (38%). Gross total resection was achieved in 69% of cases. Cranial nerve deficit was the most common post-surgical complication (71%). Most common combination of treatment included surgical resection and radiotherapy (53%). Mean overall survival was 50 months in these patients. Conclusion/Impact: Pediatric intraventricular ependymomas are rare tumors with limited information on management strategies. The mainstay of treatment is complete surgical resection. Compared to ependymomas, intraventricular ependymomas appear to have a worse overall prognosis.
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