侵袭性脑膜瘤的影像学特征、组织病理学特征和手术注意事项

G. Popescu, F. Paslaru, A. Paslaru, M. Apostol, M. Zaharia, T. Corneliu, M. Mitrica, M. Popescu, R. M. Gorgan
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摘要

脑膜瘤是主要由蛛网膜帽细胞引起的脑膜肿瘤,但在其他部位,如脑室内,它们也很少作为原发性肿瘤发生。它们占原发性颅内肿瘤的24-30%,主要影响中年或成年后的女性[1,2]。根据世界卫生组织(世界卫生组织)对中枢神经系统(CNS)肿瘤的分类,脑膜瘤可分为良性(I级,最常见类型)、非典型(II级)或间变性(III级),主要基于已知与肿瘤进展、复发风险和存活相关的组织病理学标准。由于基于世界卫生组织分类的脑膜瘤分级是决定治疗管理和肿瘤预后的最重要因素,因此增加新的标准以更好地表征这些肿瘤的兴趣越来越大。因此,2016年版世界卫生组织分类将脑侵袭作为非典型(II级)脑膜瘤诊断的独立标准[3]。然而,表现出侵袭性特征的脑膜瘤,如快速生长和较高的复发率,也可能涉及血管和骨骼。因此,作者旨在描述一种不同的实体,侵袭性脑膜瘤,在世界卫生组织的脑膜瘤细胞肿瘤分类中未被列为肿瘤表型,涉及术前、术中和术后的诊断方法,并探讨其对手术策略和辅助治疗的影响。
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Imaging characteristics, histopathological features and surgical considerations regarding aggressive meningiomas
Meningiomas are tumours of the meninges that arise primarily from arachnoidal cap cells, but they can also occur rarely as primary tumours in other localizations, such as within the ventricles. They stand for 24-30% of primary intracranial tumours and affect mostly women in their middle age or later adult life [1, 2]. Meningiomas can be classified, according to the World Health Organization (WHO) classification of Central Nervous System (CNS) tumours, as benign (grade I, most frequently encountered type), atypical (grade II) or anaplastic (grade III), based mostly on histopathological criteria known to be associated with tumour progression, recurrence risk and survival. Since meningioma grading based on the WHO classification is the most important factor determining therapeutic management and tumour prognosis, there has been an increasing interest in adding new criteria for better characterization of these tumours. Thus, the 2016 edition of the WHO classification recognized brain invasion as an independent criterion for atypical (grade II) meningioma diagnosis [3]. However, meningiomas that display aggressive features such as rapid growth and higher recurrence rate, can also involve blood vessels and bone. Hence, the authors aim to describe a different entity, aggressive meningiomas, not previously listed as a tumour phenotype in the WHO classification of meningothelial-cell tumours, with regard to pre-, intra- and postoperative methods for diagnosis and explore the implications on surgical strategies and adjuvant therapy.
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