DW-MRI of liver lesions: can a single ADC-value represent the entire lesion?

C Schmid-Tannwald1, F Dahi2, Y Jiang2

  • 1Department of Radiology, The University of Chicago, Chicago, IL, USA; Ludwig-Maximilians-University Hospital Munich, Institute for Clinical Radiology, Munich, Germany.

Clinical Radiology
|March 15, 2014
PubMed
Abstract

Insights

Focal liver lesions (FLLs) show significant variations in apparent diffusion coefficient (ADC) values within and between imaging sections. This inhomogeneity means a single ADC measurement may not accurately represent the entire FLL, impacting diagnostic interpretation.

Area of Science:

  • Radiology
  • Medical Imaging
  • Oncology

Background:

  • Focal liver lesions (FLLs) require accurate characterization for diagnosis and management.
  • Apparent diffusion coefficient (ADC) mapping in diffusion-weighted magnetic resonance imaging (DW-MRI) is a key technique for evaluating FLLs.
  • Understanding the variability of ADC values within FLLs is crucial for reliable interpretation.

Purpose of the Study:

  • To assess the homogeneity of FLLs on ADC maps.
  • To quantify the inter-section variation (range) of ADC values within FLLs.
  • To compare the inter-section ADC variability of FLLs with that of surrounding liver parenchyma.

Main Methods:

  • Retrospective analysis of abdominal DW-MRI from 88 patients with 128 FLLs (70 benign, 58 malignant).
  • Two observers evaluated intra-section and inter-section signal intensity variations within FLLs.
  • ADC values of FLLs and adjacent liver parenchyma were measured across all sections; inter-section ranges were compared.

Main Results:

  • Both benign and malignant FLLs demonstrated significant intra-section and inter-section inhomogeneity in ADC values.
  • Inter-section inhomogeneity was observed in 25.7-27.1% of benign FLLs and 50-51.7% of malignant FLLs.
  • The inter-section ADC range for both benign and malignant FLLs was significantly larger than that of the surrounding liver parenchyma.

Conclusions:

  • Intra- and inter-section variations in ADC values are common in both benign and malignant FLLs.
  • A single ADC value may not be representative of the entire FLL due to this variability.
  • These findings highlight the importance of considering ADC value heterogeneity in the interpretation of FLLs.