151. Three-Tesla dynamic contrast-enhanced MRI: a critical assessment of its use for differentiation of renal lesion subtypes.
- Author
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Sevcenco S, Ponhold L, Javor D, Kuehhas FE, Mauermann J, Miernik A, Schoenthaler M, and Baltzer PA
- Subjects
- Adult, Aged, Aged, 80 and over, Carcinoma, Renal Cell pathology, Cross-Sectional Studies, Diagnosis, Differential, Humans, Kidney Diseases pathology, Kidney Neoplasms pathology, Middle Aged, Nephrectomy, ROC Curve, Reproducibility of Results, Retrospective Studies, Sensitivity and Specificity, Carcinoma, Renal Cell diagnosis, Kidney pathology, Kidney Diseases diagnosis, Kidney Neoplasms diagnosis, Magnetic Resonance Imaging methods
- Abstract
Purpose: To evaluate the ability of dynamic contrast-enhanced (DCE) 3-T MRI for preoperative differentiation between benign and malignant renal tumors and RCC subtypes., Methods: Sixty consecutive patients undergoing preoperative DCE 3-T MRI of the kidney were evaluated in this retrospective IRB-approved evaluation. Fifty-four malignant tumors and 17 benign tumors upon surgical verification were included. Relative enhancement values of complete lesions and the most enhancing part of the lesions (hotspot) were measured using four repetitions: precontrast, arterial, venous, and delayed., Results: Mean relative enhancement patterns between malignant and benign lesions did not differ significantly during any postcontrast phase (p > 0.05). The highest mean enhancement during all postcontrast phases was identified in clear cell RCC followed by chromophobic RCC. The enhancement pattern in papillary RCC was significantly less than that of non-papillary RCC lesions. Arterial enhancement was an independent predictor for RCC subtypes (papillary vs. non-papillary, p = 0.008). The diagnostic accuracy for differentiation of papillary from non-papillary RCC based on ROC analysis was 76.4% [95% CI 62.2-87.2%]; p < 0.0001., Conclusions: Dynamic contrast-enhanced MRI at 3 T showed intermediate diagnostic capability for differentiation between papillary and non-papillary RCC subtypes but could not differentiate between benign and malignant renal lesions.
- Published
- 2014
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