Medical Academy, Lithuanian University of Health Sciences, LT50161 Kaunas, Lithuania.
Faculty of Medicine, Kaunas University of Applied Sciences, LT44162 Kaunas, Lithuania.
Curr Oncol. 2023 Aug 24;30(9):7818-7835. doi: 10.3390/curroncol30090568.
Gliomas are the most frequent intrinsic central nervous system tumors. The new 2021 WHO Classification of Central Nervous System Tumors brought significant changes into the classification of gliomas, that underline the role of molecular diagnostics, with the adult-type diffuse glial tumors now identified primarily by their biomarkers rather than histology. The status of the isocitrate dehydrogenase (IDH) 1 or 2 describes tumors at their molecular level and together with the presence or absence of 1p/19q codeletion are the most important biomarkers used for the classification of adult-type diffuse glial tumors. In recent years terminology has also changed. IDH-mutant, as previously known, is diagnostically used as astrocytoma and IDH-wildtype is used as glioblastoma. A comprehensive understanding of these tumors not only gives patients a more proper treatment and better prognosis but also highlights new difficulties. MR imaging is of the utmost importance for diagnosing and supervising the response to treatment. By monitoring the tumor on followup exams better results can be achieved. Correlations are seen between tumor diagnostic and clinical manifestation and surgical administration, followup care, oncologic treatment, and outcomes. Minimal resection site use of functional imaging (fMRI) and diffusion tensor imaging (DTI) have become indispensable tools in invasive treatment. Perfusion imaging provides insightful information about the vascularity of the tumor, spectroscopy shows metabolic activity, and nuclear medicine imaging displays tumor metabolism. To accommodate better treatment the differentiation of pseudoprogression, pseudoresponse, or radiation necrosis is needed. In this report, we present a literature review of diagnostics of gliomas, the differences in their imaging features, and our radiology's departments accumulated experience concerning gliomas.
神经胶质瘤是最常见的中枢神经系统原发性肿瘤。2021 年版世界卫生组织中枢神经系统肿瘤分类对神经胶质瘤的分类带来了重大变化,强调了分子诊断的作用,成人弥漫性神经胶质瘤肿瘤现在主要根据其生物标志物而不是组织学来识别。异柠檬酸脱氢酶(IDH)1 或 2 的状态描述了肿瘤在分子水平上的状态,并且与 1p/19q 缺失的存在与否一起,是用于成人弥漫性神经胶质瘤肿瘤分类的最重要生物标志物。近年来,术语也发生了变化。以前称为 IDH 突变型,现在在诊断上被用作星形细胞瘤,IDH 野生型被用作胶质母细胞瘤。全面了解这些肿瘤不仅为患者提供了更恰当的治疗和更好的预后,而且还凸显了新的困难。磁共振成像(MRI)对于诊断和监测治疗反应至关重要。通过在随访检查中监测肿瘤,可以取得更好的结果。肿瘤诊断与临床表现和手术管理、随访护理、肿瘤治疗和结果之间存在相关性。功能成像(fMRI)和弥散张量成像(DTI)的最小切除部位使用已成为侵袭性治疗中不可或缺的工具。灌注成像提供了关于肿瘤血管生成的深入信息,光谱显示代谢活性,核医学成像显示肿瘤代谢。为了更好地治疗,需要区分假性进展、假性反应或放射性坏死。在本报告中,我们对神经胶质瘤的诊断进行了文献回顾,讨论了它们在影像学特征上的差异,以及我们放射科积累的有关神经胶质瘤的经验。