Pierce Theodore Thomas, Provenzale James M
Duke University School of Medicine; Durham, NC, USA -
Department of Radiology, Duke University Medical Center; Durham, NC, USA, - Departments of Radiology and Imaging Sciences, Oncology and Biomedical Engineering, Emory University School of Medicine; Atlanta, GA, USA.
Neuroradiol J. 2014 Feb;27(1):63-74. doi: 10.15274/NRJ-2014-10007. Epub 2014 Feb 24.
We assess a diffusion-weighted imaging (DWI) analysis technique as a potential basis for computer-aided diagnosis (CAD) of pediatric posterior fossa tumors. A retrospective medical record search identified 103 children (mean age: 87 months) with posterior fossa tumors having a total of 126 preoperative MR scans with DWI. The minimum ADC (ADCmin) and normalized ADC (nADC) values [ratio of ADCmin values in tumor compared to normal tissue] were measured by a single observer blinded to diagnosis. Receiver operating characteristic (ROC) curves were generated to determine the optimal threshold for which the nADC and ADCmin values would predict tumor histology. Inter-rater reliability for predicting tumor type was evaluated using values measured by two additional observers. At histology, ten tumor types were identified, with astrocytoma (n=50), medulloblastoma (n=33), and ependymoma (n=9) accounting for 89%. Mean ADCmin (0.54 × 10(-3) mm(2)/s) and nADC (0.70) were lowest for medulloblastoma. Mean ADCmin (1.28 × 10(-3) mm(2)/s) and nADC (1.64) were highest for astrocytoma. For the ROC analysis, the area under the curve when discriminating medulloblastoma from other tumors using nADC was 0.939 and 0.965 when using ADCmin. The optimal ADCmin threshold was 0.66 × 10(-3) mm(2)/s, which yielded an 86% positive predictive value, 97% negative predictive value, and 93% accuracy. Inter-observer variability was very low, with near perfect agreement among all observers in predicting medulloblastoma. Our data indicate that both ADCmin and nADC could serve as the basis for a CAD program to distinguish medulloblastoma from other posterior fossa tumors with a high degree of accuracy.
我们评估了一种扩散加权成像(DWI)分析技术,作为小儿后颅窝肿瘤计算机辅助诊断(CAD)的潜在基础。一项回顾性病历检索确定了103名患有后颅窝肿瘤的儿童(平均年龄:87个月),他们共有126次术前带有DWI的磁共振成像扫描。由一名对诊断不知情的观察者测量最小表观扩散系数(ADCmin)和标准化表观扩散系数(nADC)值[肿瘤中ADCmin值与正常组织的比值]。生成受试者操作特征(ROC)曲线以确定nADC和ADCmin值预测肿瘤组织学的最佳阈值。使用另外两名观察者测量的值评估预测肿瘤类型的观察者间可靠性。在组织学检查中,确定了十种肿瘤类型,其中星形细胞瘤(n = 50)、髓母细胞瘤(n = 33)和室管膜瘤(n = 9)占89%。髓母细胞瘤的平均ADCmin(0.54×10⁻³mm²/s)和nADC(0.70)最低。星形细胞瘤的平均ADCmin(1.28×10⁻³mm²/s)和nADC(1.64)最高。对于ROC分析,使用nADC区分髓母细胞瘤与其他肿瘤时曲线下面积为0.939,使用ADCmin时为0.965。最佳ADCmin阈值为0.66×10⁻³mm²/s,其阳性预测值为86%,阴性预测值为97%,准确率为93%。观察者间变异性非常低,所有观察者在预测髓母细胞瘤方面几乎完全一致。我们的数据表明,ADCmin和nADC均可作为CAD程序的基础,以高度准确地区分髓母细胞瘤与其他后颅窝肿瘤。