Highlights
- •Algorithms perform similarly to trained subspecialists in diagnosing T2 iso- and hypointense renal mass.
- •Higher inter-reader agreement with algorithm utilization likely due to use of quantitative MR parameters
- •Substantial diagnosis-limiting overlap in the MR appearance of T2 iso- and hypointense renal masses
Abstract
Purpose
To assess if a templated algorithm can improve the diagnostic performance of MRI for
characterization of T2 isointense and hypointense renal masses.
Methods
In this retrospective study, 60 renal masses with histopathologic diagnoses that were
also confirmed as T2 iso- or hypointense on MRI were identified (mean ± standard deviation,
range: 3.9 ± 2.5, 1.0–13.7 cm). Two semi-quantitative diagnostic algorithms were created
based on MRI features of renal masses reported in the literature. Three body-MRI trained
radiologists provided clinical diagnoses based on their experience and separately
provided semiquantitative data for each components of the two algorithms. The algorithms
were applied separately by a radiology trainee without additional interpretive input.
Logistic regression was used to compare the accuracy of the three methods in distinguishing
malignant versus benign lesions and in diagnosing the exact histopathology. Inter-reader
agreement for each method was calculated using Fleiss' kappa statistics.
Results
The accuracy of the two algorithms and clinical experience were similar (70%, 69%,
and 64%, respectively, p = 0.22–0.32), with fair to moderate inter-reader agreement (Fleiss's kappa: r = 0.375, r = 0.308, r = 0.375, respectively, all p < 0.0001). The accuracy of the two algorithms and clinical experience in diagnosing
specific histopathology were also no different from each other (34%, 29%, and 32%,
respectively, p = 0.49–0.74), with fair to moderate inter-reader agreement (Fleiss's kappa: r = 0.20, r = 0.28, r = 0.375, respectively, all p < 0.0001).
Conclusion
Semi-quantitative templated algorithms based on MRI features of renal masses did not
improve the ability to diagnose T2 iso- and hypointense renal masses when compared
to unassisted interpretation by body MR trained subspecialists.
Keywords
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References
- Renal cell carcinoma: T1 and T2 signal intensity characteristics of papillary and clear cell types correlated with pathology.Am J Roentgenol. 2009; 192: 1524-1530https://doi.org/10.2214/AJR.08.1727
- Small (<4 cm) renal mass: differentiation of Angiomyolipoma without visible fat from renal cell carcinoma utilizing MR imaging.Radiology. 2012; 263: 160-168https://doi.org/10.1148/radiol.12111205
- Diagnostic performance and Interreader agreement of a standardized MR imaging approach in the prediction of small renal mass histology.Radiology. 2018; 287: 543-553https://doi.org/10.1148/radiol.2018171557
- Diagnostic accuracy of multiparametric magnetic resonance imaging to identify clear cell renal cell carcinoma in cT1a renal masses.J Urol. 2017; 198: 780-786https://doi.org/10.1016/j.juro.2017.04.089
- MRI evaluation of small (<4cm) solid renal masses: multivariate modeling improves diagnostic accuracy for angiomyolipoma without visible fat compared to univariate analysis.Eur Radiol. 2016; 26: 2242-2251https://doi.org/10.1007/s00330-015-4039-y
- Renal cortical tumors: use of multiphasic contrast-enhanced MR imaging to differentiate benign and malignant histologic subtypes.Radiology. 2012; 264: 779-788https://doi.org/10.1148/radiol.12110746
- H. Baroni R, Genega EM, Galaburda L, et al. MR classification of renal masses with pathologic correlation.Eur Radiol. 2008; 18: 365-375https://doi.org/10.1007/s00330-007-0757-0
- Hepatic arterial-phase dynamic gadolinium-enhanced MR imaging: optimization with a test examination and a power injector.Radiology. 1997; 202: 268-273https://doi.org/10.1148/radiology.202.1.8988222
- Diffusion-weighted imaging of focal renal lesions: a meta-analysis.Eur Radiol. 2014; 24: 241-249https://doi.org/10.1007/s00330-013-3004-x
- Ability and utility of diffusion-weighted MRI with different b values in the evaluation of benign and malignant renal lesions.Clin Radiol. 2011; 66: 420-425https://doi.org/10.1016/j.crad.2010.11.013
- Renal lesions: characterization with diffusion-weighted imaging versus contrast-enhanced MR imaging.Radiology. 2009; 251: 398-407https://doi.org/10.1148/radiol.2512080880
- Diffusion weighted imaging and perfusion weighted imaging in the differential diagnosis of benign and malignant renal masses on 3.0 T MRI.Zhonghua Yi Xue Za Zhi. 2015; 95: 200-204
Wang H, Cheng L, Zhang X, Wang D, Guo A, Gao Y, et al. Renal Cell Carcinoma: Diffusion-weighted MR Imaging for Subtype Differentiation at 3.0 T. Radiology 2010;257:135–43. doi:https://doi.org/10.1148/radiol.10092396.
- Segmental enhancement inversion at biphasic multidetector CT: characteristic finding of small renal Oncocytoma.Radiology. 2009; 252: 441-448https://doi.org/10.1148/radiol.2522081180
- MRI phenotype in renal cancer.Top Magn Reson Imaging. 2014; 23: 85-105https://doi.org/10.1097/RMR.0000000000000019
- Combined late gadolinium-enhanced and double-Echo chemical-shift MRI help to differentiate renal Oncocytomas with high central T2 signal intensity from renal cell carcinomas.Am J Roentgenol. 2013; 200: 830-838https://doi.org/10.2214/AJR.12.9122
- Imaging of small renal masses.Am J Roentgenol. 2000; 175: 945-955https://doi.org/10.2214/ajr.175.4.1750945
Article info
Publication history
Published online: November 05, 2020
Accepted:
October 29,
2020
Received in revised form:
October 3,
2020
Received:
August 26,
2020
Identification
Copyright
© 2020 Elsevier Inc. All rights reserved.