Tumor growth patterns in central nervous system tumors with astrocytic differentiation

Glioma Pub Date : 2020-04-01 DOI:10.4103/glioma.glioma_8_20
E. Lyutfi, Reneta Georgieva, G. Stoyanov, D. Dzhenkov
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Abstract

Background and Aim: Glial tumors with astrocytic differentiation are the most common primary malignant brain tumors. Hans Joachim Scherer established histological criteria based on hematoxylin and eosin (H&E) staining, which form the basis of the World Health Organization (WHO) glial tumor grades. The aim of this study was to investigate the incidence of Scherer structures across different classes of WHO grade tumors with astrocytic differentiation and determine whether secondary structures can be used as a grade-defining tool. Materials and Methods: Tumor samples were obtained from 36 patients with central nervous system (CNS) tumors with astrocytic differentiation between February 2018 and March 2019. The study was approved by the Committee on Ethics for Scientific Research, Medical University—Varna “Prof. Dr. Paraskev Stoyanov,” Protocol no. 20 [1] on April 26, 2012. The presence or absence of primary Scherer structures (pseudopalisading necrosis, glomeruloid vascular proliferation) and secondary Scherer structures (subpial palisading, fascicular aggregation, satellitosis around neurons, and blood vessels) was analyzed in H&E stained samples. Results: The samples were divided into two groups: 28 glioblastoma multiforme (GBM) cases and 8 lower grade astrocytoma cases. All 28 GBM cases exhibited pseudopalisading necrosis. Glomeruloid vascular proliferation was present only in 89.3% of the GBM cases. The GBM group also showed 67.9% subpial palisading, 78.5% fascicular aggregation of tumor cells, 96.4% perineuronal, and 100% perivascular satellitosis. The lower grade astrocytoma group had 0% pseudopalisading necrosis and glomeruloid vascular proliferation. Among all cases of lower grade gliomas, 50.0% showed subpial palisading, 87.5% fascicular aggregation, 100% perineuronal, and 100% perivascular satellitosis. Conclusions: Secondary Scherer structures can be considered as natural phenomena in glial tumors but cannot be used as features for grading.
星形细胞分化中枢神经系统肿瘤的生长模式
背景与目的:星形细胞分化的胶质瘤是最常见的原发性恶性脑肿瘤。Hans-Joachim Scherer根据苏木精和伊红(H&E)染色建立了组织学标准,这是世界卫生组织(世界卫生组织)胶质瘤分级的基础。本研究的目的是调查不同类别世界卫生组织星形细胞分化肿瘤中Scherer结构的发生率,并确定二级结构是否可用作分级定义工具。材料和方法:从2018年2月至2019年3月期间36例星形细胞分化的中枢神经系统(CNS)肿瘤患者中获得肿瘤样本。该研究于2012年4月26日获得了瓦尔纳医科大学科学研究伦理委员会“Paraskev Stoyanov教授博士”第20号协议[1]的批准。在H&E染色的样本中分析初级Scherer结构(假栅栏坏死、肾小球样血管增殖)和次级Scherer组织(膜下栅栏、束状聚集、神经元周围的卫星状突起和血管)的存在与否。结果:将样本分为两组:28例多形性胶质母细胞瘤(GBM)和8例低级别星形细胞瘤。28例GBM均表现为假栅栏样坏死。肾小球样血管增生仅发生在89.3%的GBM病例中。GBM组还表现出67.9%的膜下栅栏、78.5%的肿瘤细胞束聚集、96.4%的会阴和100%的血管周围卫星变性。低级别星形细胞瘤组有0%的假性栅栏状坏死和肾小球样血管增生。在所有低级别胶质瘤中,50.0%的胶质瘤表现为膜下栅栏,87.5%的胶质束聚集,100%的神经胶质瘤和100%的血管周围卫星变性。结论:继发性Scherer结构可以被认为是神经胶质瘤的自然现象,但不能作为分级的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
42 weeks
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