Meningioma: Molecular Updates from the 2021 World Health Organization Classification of CNS Tumors and Imaging Correlates.

Neetu Soni, Manish Ora, Girish Bathla, Denes Szekeres, Amit Desai, Jay J Pillai, Amit Agarwal
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Abstract

Meningiomas, the most common primary intracranial neoplasms, account for more than one-third of primary CNS tumors. While traditionally viewed as benign, meningiomas can be associated with considerable morbidity, and specific meningioma subgroups display more aggressive behavior with higher recurrence rates. The risk stratification for recurrence has been primarily associated with the World Health Organization (WHO) histopathologic grade and extent of resection. However, a growing body of literature has highlighted the value of molecular characteristics in assessing recurrence risk. While maintaining the previous classification system, the 5th edition of the 2021 WHO Classification of Central Nervous System tumors (CNS5) book expands upon the molecular information in meningiomas to help guide management. The WHO CNS5 stratifies meningioma into 3 grades (1-3) based on histopathology criteria and molecular profile. The telomerase reverse transcriptase promoter mutations and cyclin-dependent kinase inhibitor 2A/B (CDKN2A/B) deletions now signify a grade 3 meningioma with increased recurrence risk. Tumor location also correlates with underlying mutations. Cerebral convexity and most spinal meningiomas carry a 22q deletion and/or NF2 mutations, while skull base meningiomas have AKT1, TRAF7, SMO, and/or PIK3CA mutations. MRI is the primary imaging technique for diagnosing and treatment-planning of meningiomas, while DOTATATE PET imaging offers supplementary information beyond anatomic imaging. Herein, we review the evolving molecular landscape of meningiomas, emphasizing imaging/genetic biomarkers and treatment strategies relevant to neuroradiologists.

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脑膜瘤:2021 年世界卫生组织中枢神经系统肿瘤分类的分子更新及成像相关性。
脑膜瘤是最常见的原发性颅内肿瘤,占原发性中枢神经系统肿瘤的三分之一以上。虽然脑膜瘤传统上被视为良性肿瘤,但其发病率也相当高,而且特定的脑膜瘤亚群表现得更具侵袭性,复发率更高。复发风险分层主要与世界卫生组织(WHO)的组织病理学分级和切除范围有关。然而,越来越多的文献强调了分子特征在评估复发风险中的价值。2021 年第五版世界卫生组织中枢神经系统肿瘤(CNS5)一书在保留以前的分类系统的同时,扩展了脑膜瘤的分子信息,以帮助指导管理。现在,pTERT 突变和 CDKN2A/B 缺失标志着脑膜瘤 3 级,复发风险增加。肿瘤位置也与潜在的突变有关。凸面脑膜瘤和大多数脊髓脑膜瘤带有 22q 缺失和/或 NF2 突变,而颅底脑膜瘤则带有 AKT1、TRAF7、SMO 和/或 PIK3CA 突变。核磁共振成像是脑膜瘤诊断和治疗计划的主要成像方式,而 DOTATATE-PET 成像则提供了解剖成像之外的补充信息。在此,我们回顾了脑膜瘤不断发展的分子状况,强调了与神经放射科医生相关的成像/遗传生物标志物和治疗策略:AKT1=AKT丝氨酸/苏氨酸激酶1;BAP1=BRCA1相关蛋白1;CDK4/6=环素依赖性激酶4和6;KLF4=克鲁珀尔样因子4;NF2=神经纤维瘤病 2 型;PIK3CA=磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚基 alpha;POLR2A=RNA 聚合酶 II 亚基 A;SMO:SMARCB1=SWItch/sucrose non-fermentable related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1; TERT=Telomerase reverse transcriptase; TRAF7=TNF receptor-associated factor 7.
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