胶质母细胞瘤的临床特征和影像学特征,idh野生型,4级伴组织学级别较低的胶质瘤。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Kazuya Motomura, Yuji Kibe, Fumiharu Ohka, Kosuke Aoki, Junya Yamaguchi, Ryuta Saito
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引用次数: 0

摘要

2021年世界卫生组织(WHO)中枢神经系统肿瘤分类采用分子标准,进一步整合了胶质瘤的组织学和分子诊断。这种分类允许诊断异柠檬酸脱氢酶野生型(IDHwt)胶质母细胞瘤(GBM)和WHO分级4级组织学级别较低的胶质瘤(LrGGs),即使没有高级别的组织病理学特征,如坏死和/或微血管增生。它们至少包含以下一种分子特征:表皮生长因子受体扩增,染色体7增加/10减少,或端粒酶逆转录酶启动子突变。在组织学诊断时的影像学特征中,在这些肿瘤中经常观察到脑胶质瘤病的生长模式。此外,这种生长模式在IDHwt GBM, WHO分级4,组织学分级II的胶质瘤中明显更高。尽管IDHwt GBM (WHO 4级)伴组织学LGGs的确切预后尚不清楚,但其生存期与组织学IDHwt GBM (WHO 4级)相似,尽管其组织病理学特征与IDHmut LrGGs相似。这些发现加强了对分子特征分析的需求,无论是否表现出与IDHmut lrgg相似的临床特征和影像学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical characteristics and radiological features of glioblastoma, IDH-wildtype, grade 4 with histologically lower-grade gliomas.

Clinical characteristics and radiological features of glioblastoma, IDH-wildtype, grade 4 with histologically lower-grade gliomas.

The 2021 World Health Organization (WHO) classification of central nervous system tumors applied molecular criteria and further integrated histological and molecular diagnosis of gliomas. This classification allows for the diagnosis of isocitrate dehydrogenase wild-type (IDHwt) glioblastoma (GBM), and WHO grade 4 with histologically lower-grade gliomas (LrGGs), even in the absence of high-grade histopathologic features, such as necrosis and/or microvascular proliferation. They contain at least one of the following molecular features: epidermal growth factor receptor amplification, chromosome 7 gain/10 loss, or telomerase reverse transcriptase promoter mutation. In the imaging features at the time of histological diagnosis, a gliomatosis cerebri growth pattern was frequently observed in these tumors. Furthermore, this growth pattern was significantly higher in IDHwt GBM, WHO grade 4, with histological grade II gliomas. Although the exact prognosis of IDHwt GBM, WHO grade 4, with histologically LGGs remains unknown, its OS was approximately 1-2 years similar to that of histologically IDHwt GBM, WHO grade 4, despite histopathological features similar to IDHmut LrGGs. These findings reinforce the need for the analysis of molecular features, regardless of presenting similar clinical characteristics and imaging features to IDHmut LrGGs.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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