Imaging the renal lesion with dual-energy multidetector CT and multi-energy applications in clinical practice: what can it truly do for you?

Published

Journal Article (Review)

OBJECTIVE: Many fortuitously detected renal lesions are incompletely characterised at traditional MDCT imaging, thus posing daily challenges to radiologists and referring physicians. There is burgeoning evidence that dual-energy MDCT and multi-energy applications provide an added value over traditional MDCT imaging in renal lesion characterisation and throughput. This special report gives a vendor-neutral outlook on technical essentials, recommended protocols, high-yield clinical opportunities and reviews radiation dose aspects of dual-energy MDCT imaging and multi-energy applications in renal lesions. In addition to a guide on interpretative traps and emerging problems, we provide an update on new, potential imaging horizons. CONCLUSION: Dual-energy MDCT and multi-energy applications can facilitate the imaging interpretation and throughput of renal lesions. Conjointly with capitalisation on the benefits, familiarity with dual- and multi-energy data sets as well as continuous scrutiny of interpretative traps can be the keys to the successful implementation and enhanced clinical acceptance of this powerful technique in the imaging community. Continuous advances in hardware and computer interfaces are expected to pave the way for the further expansion of the application spectrum. KEY POINTS: • Optimal protocols must be adopted for leveraging dual-energy benefits in renal imaging. • Virtual monochromatic imaging can overcome renal cyst pseudoenhancement. • Iodine maps help to interpret renal lesions incompletely characterised at traditional MDCT. • Interpretative traps need to be weighed-up in dual-energy renal lesions imaging. • Technical advances are expanding the dual-energy applications spectrum for renal lesions imaging.

Full Text

Duke Authors

Cited Authors

  • Mileto, A; Sofue, K; Marin, D

Published Date

  • October 2016

Published In

Volume / Issue

  • 26 / 10

Start / End Page

  • 3677 - 3690

PubMed ID

  • 26801162

Pubmed Central ID

  • 26801162

Electronic International Standard Serial Number (EISSN)

  • 1432-1084

Digital Object Identifier (DOI)

  • 10.1007/s00330-015-4180-7

Language

  • eng

Conference Location

  • Germany