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少突胶质细胞瘤:当前的概念、误解及传闻

Oligodendroglial neoplasms: current concepts, misconceptions, and folklore.

作者信息

Perry A

机构信息

Washington University School of Medicine, St Louis, Missouri 63110-1093, USA.

出版信息

Adv Anat Pathol. 2001 Jul;8(4):183-99. doi: 10.1097/00125480-200107000-00001.

Abstract

Given current prognostic and therapeutic implications, the accurate classification and grading of oligodendroglial neoplasms has become critical. However, the prevalence of morphologically ambiguous gliomas, subjective histologic criteria, personal biases, oligodendroglioma mimics, and the lack of specific oligodendroglioma markers has led to high interobserver variability and created a contentious problem encountered daily in active surgical neuropathology practices. Since histologic assessment is still a powerful prognosticator, it appropriately remains the diagnostic gold standard. However, recent efforts have focused on identifying the most reproducible and clinically relevant criteria, standardizing classification and grading schemes, and searching for useful ancillary biologic and genetic markers capable of further stratifying an otherwise heterogeneous patient population. This paper reviews the morphologic and genetic spectrum of oligodendroglial neoplasms, recent diagnostic and prognostic developments, and potential future directions.

摘要

鉴于当前的预后和治疗意义,少突胶质细胞瘤的准确分类和分级已变得至关重要。然而,形态学上模棱两可的胶质瘤的普遍性、主观的组织学标准、个人偏见、少突胶质细胞瘤的模仿物以及缺乏特异性的少突胶质细胞瘤标志物,导致了观察者间的高度变异性,并在活跃的外科神经病理学实践中造成了一个每天都会遇到的有争议的问题。由于组织学评估仍然是一个强大的预后指标,它理所当然地仍然是诊断的金标准。然而,最近的努力集中在确定最可重复和临床相关的标准、规范分类和分级方案,以及寻找能够进一步对原本异质性的患者群体进行分层的有用辅助生物学和基因标志物。本文综述了少突胶质细胞瘤的形态学和基因谱、近期的诊断和预后进展以及潜在的未来方向。

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