Herneth Andreas M, Guccione Samira, Bednarski Mark
Department of Radiology, Division of Muskulo Skeletal Radiology, University of Vienna, AKH-7F Währinger Gürtel 18-20, A-1090 Vienna, Austria.
Eur J Radiol. 2003 Mar;45(3):208-13. doi: 10.1016/s0720-048x(02)00310-8.
The purpose of the this study was to evaluate the potential of diffusion weighted imaging (DWI) to distinguish different tissue compartments in early, intermediate and advanced tumor stages.
Twenty-two male mice were induced with squamous cell tumor (SCCVII) and scanned with a clinical 1.5 T scanner. T1-SE, T2-FSE, diffusion weighted Line-Scan-MRI and contrast enhanced T1-SE were obtained from mice with early (tumor volume 10-100 mm(3)), intermediate (200-600 mm(3)), advanced tumors (600-1000 mm(3)) and tumor necrosis (>1500 mm(3)). The apparent diffusion coefficient (ADC) of different tumor compartments was calculated offline with a pixel-by-pixel method. The animals were sacrificed immediately after scanning and histopathologic correlation was performed.
In early stages of tumor development, tumors appeared homogeneous on diffusion weighted images with an ADC of 0.64+/-0.06 x 10(-3) mm(2)/s. With tumor progression the ADC in the rim areas of tumor increased significantly (intermediate stage: 0.70+/-0.11 x 10(-3) mm(2)/s; advanced stage: 0.88+/-0.11 x 10(-3) mm(2)/s; tumor necrosis 1.03+/-0.06 x 10(-3) mm(2)/s), whereas the ADC in viable tumor remained constant. Histologically the areas with an increased ADC correlated well with areas of necrosis (reduced cell density).
The ADC is a non-invasive technique to monitor changes in the biological structure of tumor tissue during tumor progression. Thus, DWI is a potential diagnostic tool for in-vivo tissue characterization.
本研究的目的是评估扩散加权成像(DWI)在区分早期、中期和晚期肿瘤阶段不同组织成分方面的潜力。
22只雄性小鼠被诱导产生鳞状细胞肿瘤(SCCVII),并用临床1.5T扫描仪进行扫描。对早期(肿瘤体积10 - 100立方毫米)、中期(200 - 600立方毫米)、晚期肿瘤(600 - 1000立方毫米)和肿瘤坏死(>1500立方毫米)的小鼠进行T1加权自旋回波(T1-SE)、T2加权快速自旋回波(T2-FSE)、扩散加权线扫描磁共振成像(Line-Scan-MRI)和对比增强T1-SE检查。采用逐像素法离线计算不同肿瘤区域的表观扩散系数(ADC)。扫描后立即处死动物并进行组织病理学相关性分析。
在肿瘤发展的早期阶段,肿瘤在扩散加权图像上表现为均匀性,ADC为0.64±0.06×10⁻³平方毫米/秒。随着肿瘤进展,肿瘤边缘区域的ADC显著增加(中期:0.70±0.11×10⁻³平方毫米/秒;晚期:0.88±0.11×10⁻³平方毫米/秒;肿瘤坏死:1.03±0.06×10⁻³平方毫米/秒),而存活肿瘤中的ADC保持不变。组织学上,ADC增加的区域与坏死区域(细胞密度降低)相关性良好。
ADC是一种监测肿瘤进展过程中肿瘤组织生物学结构变化的非侵入性技术。因此,DWI是一种潜在的体内组织特征诊断工具。