3-特斯拉酰胺质子转移加权成像(APT-WI):肿瘤模拟物中的信号也升高。

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
European Radiology Pub Date : 2025-06-01 Epub Date: 2024-11-26 DOI:10.1007/s00330-024-11202-8
Guillaume Hamon, Augustin Lecler, Jean-Christophe Ferré, Pierre Bourdillon, Loïc Duron, Julien Savatovsky
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引用次数: 0

摘要

目的通过系统报告肿瘤模拟物和脑肿瘤的APTwi信号强度(APT-SI),探索酰胺质子转移加权成像(APTwi)在临床实践中用于脑肿块的初步分类:单中心回顾性分析(2017-2020年)156名患者(84名男性,平均年龄:50.9±20岁)的APTwi,这些患者在接受任何治疗前使用3-特斯拉磁共振成像对脑肿块进行了特征成像。125/156(80%)名患者患有脑肿瘤,31/156(20%)名患者患有肿瘤模拟物。由两名阅读者在二维轴切片上手动绘制病变区和周围区的 APTwi 图,并系统报告与 3.5 ppm 磁化转移比不对称相对应的 APT-SI。采用学生 t 检验或 Wilcoxon 检验来比较患者组别:结果:与模拟肿瘤相比,肿瘤病变区和周围区域的平均 APT-SI 明显更高:3% [2.10-4](中位数 [Q1-Q3]) vs 1.7% [0.80-2.55](P 结论:ATPwi 上的高信号并不代表肿瘤病变区和周围区域的高信号:ATPwi上的高信号并非高级别脑肿瘤所独有,在一些肿瘤模拟物和低级别肿瘤亚型中也可观察到:问题 酰胺质子转移加权成像(APTwi)在脑肿块分类中的价值是什么?研究结果 脑肿块肿瘤核心的高 APT 信号强度可能与高级别或低级别肿瘤或肿瘤模拟物相对应。临床意义 在对患者进行脑肿块初步分类时,应谨慎解释 APTwi 结果,并结合其他 MRI 参数,因为 APTwi 信号高并不一定表示肿瘤等级高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
3-Tesla amide proton transfer-weighted imaging (APT-WI): elevated signal also in tumor mimics.

Objectives: To explore amide proton transfer-weighted imaging (APTwi) for the initial classification of brain masses in clinical practice by systematically reporting APTwi signal intensity (APT-SI) in tumor mimics and brain tumors.

Materials and methods: Single-center retrospective analysis (2017-2020) of APTwi in 156 patients (84 men, mean age: 50.9 ± 20) who underwent characterization imaging of a brain mass prior to any treatment, using 3-Tesla MRI. 125/156 (80%) patients presented with brain tumor and 31/156 (20%) with tumor mimics. Regions of interest were manually drawn on 2D axial slices by two readers on APTwi map in lesional and perilesional areas and APT-SI, corresponding to the Magnetization Transfer Ratio asymmetry at 3.5 ppm, was systematically reported. Student's t-test or Wilcoxon-test were used to compare groups of patients.

Results: The mean APT-SI in lesional and perilesional areas were significantly higher in tumors compared to tumor mimics: 3% [2.10-4] (median [Q1-Q3]) vs 1.7% [0.80-2.55] (p < 0.001) and 1.9% [1.2-2.80] vs. 1.0% [0.55-2.3] (p < 0.01). There were no differences in mean APT-SI in the tumor core between low and high-grade tumors: 2.5% [1.80-4.0] vs. 3.25% [2.5-4.0]. The mean APT-SI was significantly higher in high-grade glioma compared to low-grade glioma: 3.4% [2.7-4] vs. 2.1% [1.7-2.5] (p < 0.001). Highest mean APT-SI in tumor core were found in mesenchymal tumors (5.83% ± 1.45, mean ± SD), embryonal tumors (5.27% ± 3.5) and meningiomas (4.28% ± 0.70). In tumor mimics, highest mean APT-SI was found in the core of infectious lesions (3.52% ± 0.67).

Conclusion: High signal on ATPwi is not exclusive to high-grade brain tumors but can be observed in some tumor mimics and subtypes of low-grade tumors.

Key points: Question What is the value of amide proton transfer-weighted imaging (APTwi) in the setting of brain mass classification? Findings High APT-signal intensity in the tumor core of a brain mass could correspond to a high- or low-grade tumor or tumor mimic. Clinical relevance In patients presenting for the initial classification of brain masses, APTwi findings should be interpreted with caution and in conjunction with other MRI parameters, as a high APTwi signal does not necessarily indicate a high-grade tumor.

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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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