Sensitivity and specificity of unenhanced MR mammography (DWI combined with T2-weighted TSE imaging, ueMRM) for the differentiation of mass lesions

被引:107
作者
Baltzer, Pascal A. T. [1 ]
Benndorf, Matthias [1 ]
Dietzel, Matthias [1 ]
Gajda, Mieczyslaw [2 ]
Camara, Oumar [3 ]
Kaiser, Werner A. [1 ]
机构
[1] Univ Jena, Inst Diagnost & Intervent Radiol, D-07740 Jena, Germany
[2] Univ Jena, Inst Pathol, D-07740 Jena, Germany
[3] Univ Jena, Clin Gynecol, D-07740 Jena, Germany
关键词
DWI; Sensitivity and specificity; Breast; MRI; DCE-MRI; INTRAVENOUS GADOLINIUM-DTPA; BREAST-CANCER; INTERPRETATION MODEL; TUMORS; ADC; CARCINOMA; CONTRAST; BENIGN;
D O I
10.1007/s00330-009-1654-5
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
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 a parts per thousand yenaEuro parts per thousand 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.
引用
收藏
页码:1101 / 1110
页数:10
相关论文
共 32 条
[1]   Gadolinium-based contrast agents and nephrogenic systemic fibrosis: a systematic review and meta-analysis [J].
Agarwal, Rajender ;
Brunelli, Steven M. ;
Williams, Kendal ;
Mitchell, Matthew D. ;
Feldman, Harold I. ;
Umscheid, Craig A. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2009, 24 (03) :856-863
[2]   STATISTICS NOTES - DIAGNOSTIC-TESTS-1 - SENSITIVITY AND SPECIFICITY .3. [J].
ALTMAN, DG ;
BLAND, JM .
BRITISH MEDICAL JOURNAL, 1994, 308 (6943) :1552-1552
[3]  
Altmann DG., 1991, Practical Statistics for Medical Research
[4]   Diffusion-weighted imaging (DWI) in MR mammography (MRM): clinical comparison of echo planar imaging (EPI) and half-Fourier single-shot turbo spin echo (HASTE) diffusion techniques [J].
Baltzer, P. A. T. ;
Renz, D. M. ;
Herrmann, K. -H. ;
Dietzel, M. ;
Krumbein, I. ;
Gajda, M. ;
Camara, O. ;
Reichenbach, J. R. ;
Kaiser, W. A. .
EUROPEAN RADIOLOGY, 2009, 19 (07) :1612-1620
[5]   Extracellular gadolinium-based contrast media: An overview [J].
Bellin, Marie-France ;
Van Der Molen, Aart J. .
EUROPEAN JOURNAL OF RADIOLOGY, 2008, 66 (02) :160-167
[6]  
Charles-Edwards Elizabeth M, 2006, Cancer Imaging, V6, P135, DOI 10.1102/1470-7330.2006.0021
[7]   Intravenous administration of Gd-DTPA prior to DWI does not affect the apparent diffusion constant [J].
Chen, G ;
Jespersen, SN ;
Pedersen, M ;
Pang, Q ;
Horsman, MR ;
Stodkilde-Jorgensen, H .
MAGNETIC RESONANCE IMAGING, 2005, 23 (05) :685-689
[8]   Echoplanar diffusion-weighted MRI with intravenous gadolinium-DTPA [J].
Fitzek, C ;
Mentzel, HJ ;
Fitzek, S ;
Sauner, D ;
Kaiser, WA ;
Reichenbach, JR .
NEURORADIOLOGY, 2003, 45 (09) :592-597
[9]   Differentiation of clinically benign and malignant breast lesions using diffusion-weighted imaging [J].
Guo, Y ;
Cai, YQ ;
Cai, ZL ;
Gao, YG ;
An, NY ;
Ma, L ;
Mahankali, S ;
Gao, JH .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 16 (02) :172-178
[10]  
Hatakenaka Masamitsu, 2008, Magn Reson Med Sci, V7, P23, DOI 10.2463/mrms.7.23