4级星形细胞瘤vs 4级胶质母细胞瘤:H&E有什么线索吗?

IF 1.7 4区 医学 Q4 NEUROSCIENCES
Cevriye Cansiz Ersöz, Havva Berber, Aylin Heper
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引用次数: 0

摘要

胶质瘤是中枢神经系统最常见的原发性肿瘤。世界卫生组织(WHO)第五版中枢神经系统肿瘤分类将IDH突变型星形细胞瘤4级和IDH野生型胶质母细胞瘤4级确定为不同的实体。本研究旨在从两组50例患者中确定可以预测4级弥漫性星形细胞瘤和4级胶质母细胞瘤中IDH突变状态的形态学指标。使用数字扫描仪扫描苏木精和伊红(H&E)染色的肿瘤切片,并在数字图像上进行进一步的组织病理学检查,并进行额外的计算和测量。研究表明,idh野生型胶质母细胞瘤和idh突变4级星形细胞瘤表现出独特的形态学特征,特别是在坏死水平、微血管密度和“C”或“环”形巨细胞的存在方面。尽管基因组生物标志物技术取得了进步,但组织学仍然是预测患者预后的重要工具。因此,病理学家必须继续研究和记录中枢神经系统肿瘤分子变化的形态学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Grade 4 astrocytoma vs. grade 4 glioblastoma: is there any clue in H&E?

Objective: Gliomas are the most common primary tumors of the central nervous system. The fifth edition of the World Health Organization (WHO) Classification of Tumors of the CNS identifies IDH mutant astrocytomas grade 4 and IDH wild type glioblastomas grade 4 as distinct entities. This study aimed to identify morphological indicators that could predict IDH mutation status in grade 4 diffuse astrocytomas and grade 4 glioblastomas among fifty patients from two groups.

Methods: Hematoxylin and eosin (H&E)-stained tumor slides were scanned using a digital scanner and further histopathological examinations were performed on digital images, with additional calculations and measurements.

Results: The study showed that, IDH-wildtype glioblastomas and IDH-mutant grade 4 astrocytomas exhibit unique morphological features, particularly in relation to levels of necrosis, microvessel density, and the presence of "C" or "Ring" shape giant cells.

Conclusion: Despite advancements in genomic biomarker technology, histology remains an essential tool for predicting patient outcomes. Therefore, pathologists must continue to investigate and document the morphological implications of molecular changes in CNS tumors.

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来源期刊
CiteScore
5.10
自引率
0.00%
发文量
132
审稿时长
2 months
期刊介绍: The International Journal of Neuroscience publishes original research articles, reviews, brief scientific reports, case studies, letters to the editor and book reviews concerned with problems of the nervous system and related clinical studies, epidemiology, neuropathology, medical and surgical treatment options and outcomes, neuropsychology and other topics related to the research and care of persons with neurologic disorders.  The focus of the journal is clinical and transitional research. Topics covered include but are not limited to: ALS, ataxia, autism, brain tumors, child neurology, demyelinating diseases, epilepsy, genetics, headache, lysosomal storage disease, mitochondrial dysfunction, movement disorders, multiple sclerosis, myopathy, neurodegenerative diseases, neuromuscular disorders, neuropharmacology, neuropsychiatry, neuropsychology, pain, sleep disorders, stroke, and other areas related to the neurosciences.
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