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成人弥漫性胶质瘤队列中 T2-FLAIR 不匹配模式及经典 T2-FLAIR 不匹配征象的偏离。

Patterns of T2-FLAIR discordance across a cohort of adult-type diffuse gliomas and deviations from the classic T2-FLAIR mismatch sign.

机构信息

Division of Neuroradiology, Department of Medical Imaging, St. Michael's Hospital, University of Toronto, 30 Bond St., Toronto, ON, M5B 1W8, Canada.

Diagnostic and Interventional Radiology Department, Assiut University, Asyut, Egypt.

出版信息

Neuroradiology. 2024 Apr;66(4):521-530. doi: 10.1007/s00234-024-03297-z. Epub 2024 Feb 13.

Abstract

PURPOSE

T2-FLAIR mismatch serves as a highly specific but insensitive marker for IDH-mutant (IDHm) astrocytoma with potential limitations in real-world application. We aimed to assess the utility of a broader definition of T2-FLAIR discordance across a cohort of adult-type diffuse lower-grade gliomas (LrGG) to see if specific patterns emerge and additionally examine factors determining deviation from the classic T2-FLAIR mismatch sign.

METHODS

Preoperative MRIs of non-enhancing adult-type diffuse LrGGs were reviewed. Relevant demographic, molecular, and MRI data were compared across tumor subgroups.

RESULTS

Eighty cases satisfied the inclusion criteria. Highest discordance prevalence and > 50% T2-FLAIR discordance volume were noted with IDHm astrocytomas (P < 0.001), while < 25% discordance volume was associated with oligodendrogliomas (P = 0.03) and IDH-wildtype (IDHw) LrGG (P = 0.004). "T2-FLAIR matched pattern" was associated with IDHw LrGG (P < 0.001) and small or minimal areas of discordance with oligodendrogliomas (P = 0.03). Sensitivity and specificity of classic mismatch sign for IDHm astrocytoma were 25.7% and 100%, respectively (P = 0.06). Retained ATRX expression and/or non-canonical IDH mutation (n = 10) emerged as a significant factor associated with absence of classic T2-FLAIR mismatch sign in IDHm astrocytomas (100%, P = 0.02) and instead had minimal discordance or matched pattern (40%, P = 0.04).

CONCLUSION

T2-FLAIR discordance patterns in adult-type diffuse LrGGs exist on a diverging but distinct spectrum of classic mismatch to T2-FLAIR matched patterns. Specific molecular markers may play a role in deviations from classic mismatch sign.

摘要

目的

T2-FLAIR 不匹配是 IDH 突变型(IDHm)星形细胞瘤的一个高度特异但不敏感的标志物,在实际应用中可能存在局限性。我们旨在评估在一组成人型弥漫性低级别胶质瘤(LrGG)中,更广泛的 T2-FLAIR 不匹配定义的效用,以观察是否出现特定模式,并进一步研究决定偏离经典 T2-FLAIR 不匹配征象的因素。

方法

回顾性分析非增强成人型弥漫性 LrGG 的术前 MRI。比较肿瘤亚组的相关人口统计学、分子和 MRI 数据。

结果

80 例符合纳入标准。IDHm 星形细胞瘤的不匹配发生率最高(P<0.001),且>50% T2-FLAIR 不匹配体积;而<25%不匹配体积与少突胶质细胞瘤(P=0.03)和 IDH 野生型(IDHw)LrGG(P=0.004)相关。“T2-FLAIR 匹配模式”与 IDHw LrGG 相关(P<0.001),与少突胶质细胞瘤的小或最小面积不匹配相关(P=0.03)。经典不匹配征象对 IDHm 星形细胞瘤的敏感性和特异性分别为 25.7%和 100%(P=0.06)。保留 ATRX 表达和/或非典型 IDH 突变(n=10)是与 IDHm 星形细胞瘤中经典 T2-FLAIR 不匹配征象缺失相关的重要因素(100%,P=0.02),而是具有最小的不匹配或匹配模式(40%,P=0.04)。

结论

成人型弥漫性 LrGG 中 T2-FLAIR 不匹配模式存在于经典不匹配到 T2-FLAIR 匹配模式的离散但不同的光谱上。特定的分子标志物可能在偏离经典不匹配征象中发挥作用。

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