Institute of Diagnostic and Interventional Radiology, Friedrich Schiller University Jena, Erlanger Allee 101, 07740, Jena, Germany.
Eur Radiol. 2010 May;20(5):1101-10. doi: 10.1007/s00330-009-1654-5. Epub 2009 Nov 20.
This study was performed to assess the sensitivity and specificity for malignant and benign mass lesions of a diagnostic approach combining DWI with T2-weighted images (unenhanced MR mammography, ueMRM) and compare the results with contrast-enhanced MR mammography (ceMRM).
Consecutive patients undergoing histopathological verification of mass lesions after MR mammography without prior breast interventions (contrast-enhanced T1-weighted, T2-weighted and DWI sequences) were eligible for this retrospective investigation. Two blinded observers first rated ueMRM and then ceMRM according to the BIRADS scale. Lesion size, ADC values and T2-weighted TSE descriptors were assessed.
This study examined 81 lesions (27 benign, 54 malignant). Sensitivity of ueMRM was 93% (observer 1) and 86% (observer 2), respectively. Sensitivity of ceMRM was 96.5% (observer 1) and 98.3% (observer 2). Specificity was 85.2% (ueMRM) and 92.6% (ceMRM) for both observers. The differences between both methods and observers were not significant (P > or = 0.09). Lesion size measurements did not differ significantly among all sequences analyzed. Tumor visibility was worse using ueMRM for both benign (P < 0.001) and malignant lesions (P = 0.004).
Sensitivity and specificity of ueMRM in mass lesions equal that of ceMRM. However, a reduced lesion visibility in ueMRM may lead to more false-negative findings.
本研究旨在评估弥散加权成像(DWI)与 T2 加权图像(未增强磁共振乳腺成像,ueMRM)相结合的诊断方法对良、恶性肿块病变的敏感性和特异性,并将结果与对比增强磁共振乳腺成像(ceMRM)进行比较。
本回顾性研究纳入了连续接受 MR 乳腺成像且无先前乳腺介入(对比增强 T1 加权、T2 加权和 DWI 序列)的肿块病变患者。两位观察者首先根据 BIRADS 量表对 ueMRM 和 ceMRM 进行评分,然后评估病灶大小、ADC 值和 T2 加权 TSE 描述符。
本研究共纳入 81 个病灶(27 个良性,54 个恶性)。ueMRM 的观察者 1 和观察者 2 的敏感性分别为 93%和 86%,ceMRM 的敏感性分别为 96.5%和 98.3%。两位观察者的特异性分别为 ueMRM 的 85.2%和 ceMRM 的 92.6%。两种方法和观察者之间的差异无统计学意义(P≥0.09)。在所有分析的序列中,病灶大小测量值无显著差异。与 ceMRM 相比,ueMRM 对良性(P<0.001)和恶性病变(P=0.004)的病灶显示更差。
ueMRM 在肿块病变中的敏感性和特异性与 ceMRM 相当。然而,ueMRM 中病灶的可见度降低可能导致更多的假阴性结果。