Extracranial Meningioma Metastasis: A Systematic Review of Clinical Characteristics, Management Strategies, and Outcomes

Mohammad Faizan Khan, Kurtis Young, Erin Rauber, Christian T. Ogasawara, G. Umana, Paolo Palmisciano, Gina Watanabe
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Abstract

Background: Meningioma is the most common type of intracranial neoplasm, accounting for approximately 40% of all primary brain tumors. Although these tumors are usually benign and slow-growing, extracranial metastasis can occur in less than 1% of cases. Due to the rarity, diagnosis can pose a challenge. In this systematic review, we summarize and analyze patient demographics, clinical characteristics, management strategies, and outcomes of patients with extracranial meningioma metastasis. Project Methods: A systematic review was performed following the (PRISMA) guidelines. PubMed, Ovid EMBASE, Cochrane, Scopus, and Web of Science databases were searched. Clinical characteristics, management, and outcomes were analyzed. Results: A total of 127 studies with 164 patients were included. There were 51% males and mean age of primary tumor diagnosis was 48 years (range, 8-91). Primary tumors were mostly located on the convexity of the brain (52%) and WHO grade 1 (38%) or grade 2 (37%). Histological findings were predominantly atypical (37%). Mean number of intracranial recurrences was 2 (range, 0-7) and occurred in 81% of cases. Average time between primary tumor and the first extracranial metastasis was 103 months (range, 2-450). The top three most common locations of metastases were the lungs (39%), spine (15%), and liver (12%). Most often, there was no change in grade (68%) from the primary tumor to the first metastasis. Gross total resection of the primary tumor was achieved in 76% of cases. Mean survival from primary diagnosis and survival from first metastasis was 118 and 31 months, respectively. Conclusion/Impact: Mechanisms by which extracranial meningioma metastasis occur are still unclear, though do not appear to involve evolution into a more aggressive histologic type in most cases. In a patient with a history of intracranial meningioma recurrence and symptoms of lung, spine, or liver, dysfunction, extracranial meningioma metastasis should be considered within the differential.
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颅外脑膜瘤转移:临床特征、管理策略和结果的系统回顾
背景:脑膜瘤是最常见的颅内肿瘤,约占所有原发性脑肿瘤的 40%。虽然这些肿瘤通常是良性的,生长缓慢,但只有不到1%的病例会发生颅外转移。由于其罕见性,诊断可能是一项挑战。在这篇系统性综述中,我们总结并分析了颅外脑膜瘤转移患者的人口统计学特征、临床特征、管理策略和预后。项目方法:按照(PRISMA)指南进行系统性综述。检索了 PubMed、Ovid EMBASE、Cochrane、Scopus 和 Web of Science 数据库。对临床特征、管理和结果进行了分析。结果:共纳入了 127 项研究,164 名患者。男性占 51%,原发性肿瘤诊断的平均年龄为 48 岁(8-91 岁)。原发性肿瘤大多位于大脑凸面(52%),WHO分级为1级(38%)或2级(37%)。组织学结果以非典型为主(37%)。颅内复发的平均次数为 2 次(0-7 次不等),占 81% 的病例。原发肿瘤与首次颅外转移之间的平均间隔时间为 103 个月(2-450 个月)。最常见的前三个转移部位分别是肺部(39%)、脊柱(15%)和肝脏(12%)。大多数情况下,从原发肿瘤到第一个转移灶的分级没有变化(68%)。76%的病例实现了原发肿瘤的全切除。从原发诊断到首次转移的平均生存期分别为 118 个月和 31 个月。结论/影响:颅外脑膜瘤转移的发生机制尚不清楚,但在大多数病例中似乎并不涉及演变为更具侵袭性的组织学类型。对于有颅内脑膜瘤复发史和肺部、脊柱或肝脏功能障碍症状的患者,在鉴别时应考虑颅外脑膜瘤转移。
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