University Hospital of Saint Etienne, North Hospital, Department of Pathology, Saint Etienne, France.
Mines Saint-Etienne, Univ Clermont Auvergne, CNRS, LIMOS, Centre CIS, Saint-Etienne, France.
Pathology. 2021 Aug;53(5):602-607. doi: 10.1016/j.pathol.2020.10.024. Epub 2021 Feb 20.
Meningioma grading relies on several pathological criteria (brain invasion, mitotic count, sheeting, small cell foci, necrosis, macronucleoli and hypercellularity) and histopathological subtypes. Regardless of histopathological subtype, the presence of these pathological parameters can be focally present and not present on each slide of a meningioma. We performed (1) a retrospective work comparing the frequency of parameters used for meningioma grading between two periods with different sampling techniques, and (2) we calculated the probability of presence of each criterion on resected meningiomas entirely processed included and examined. First, we compared two time periods: between 2002-2008 where meningiomas were not all entirely sampled, and between 2012-2018 where all meningiomas were entirely sampled. The frequency of tumour grades was not significantly different between the two periods (p=0.17). Mitosis ≥4/1.6mm, small cell foci, macronucleoli and hypercellularity were more frequently found when meningiomas were entirely sampled (p<0.05). Second, we focused on 59 grade 2 meningiomas entirely sampled to highlight the distribution of histopathological parameters used for meningioma grading. We have shown that a correct grading of more than 95% of meningiomas can be achieved when at least six slides are examined. Our work suggests that meningioma sampling might be an issue and the sampling system must be specified in research works on grading.
脑膜瘤的分级依赖于几个病理学标准(脑侵犯、有丝分裂计数、片状、小细胞灶、坏死、巨核细胞和细胞丰富度)和组织病理学亚型。无论组织病理学亚型如何,这些病理学参数的存在可能是局灶性的,而不是脑膜瘤的每一张切片都存在。我们进行了(1)一项回顾性工作,比较了两种不同采样技术时期用于脑膜瘤分级的参数频率,以及(2)我们计算了在完全处理和检查的切除脑膜瘤中每个标准存在的概率。首先,我们比较了两个时期:2002-2008 年期间脑膜瘤未全部进行完全采样,以及 2012-2018 年期间所有脑膜瘤均进行了完全采样。两个时期之间肿瘤分级的频率没有显著差异(p=0.17)。当脑膜瘤进行完全采样时,有丝分裂≥4/1.6mm、小细胞灶、巨核细胞和细胞丰富度更常见(p<0.05)。其次,我们专注于 59 例完全采样的 2 级脑膜瘤,以突出用于脑膜瘤分级的组织病理学参数的分布。我们已经表明,当至少检查 6 张切片时,可以正确分级超过 95%的脑膜瘤。我们的工作表明,脑膜瘤采样可能是一个问题,在分级的研究工作中必须指定采样系统。