Differentiating Well-Differentiated from Poorly-Differentiated HCC: The Potential and the Limitation of Gd-EOB-DTPA in the Presence of Liver Cirrhosis

Author:

Goetz Andrea1,Verloh Niklas2ORCID,Utpatel Kirsten3,Fellner Claudia1,Rennert Janine1ORCID,Einspieler Ingo1,Doppler Michael2,Luerken Lukas4ORCID,Alizadeh Leona S.5ORCID,Uller Wibke2ORCID,Stroszczynski Christian1,Haimerl Michael4

Affiliation:

1. Department of Radiology, University Hospital Regensburg, 93053 Regensburg, Germany

2. Department of Diagnostic and Interventional Radiology, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, 79085 Freiburg, Germany

3. Department of Pathology, University Regensburg, 93053 Regensburg, Germany

4. Department of Radiology, Klinikum Würzburg Mitte, 97074 Würzburg, Germany

5. Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, 60596 Frankfurt am Main, Germany

Abstract

This study uses magnetic resonance imaging (MRI) to investigate the potential of the hepatospecific contrast agent gadolinium ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA) in distinguishing G1- from G2/G3-differentiated hepatocellular carcinoma (HCC). Our approach involved analyzing the dynamic behavior of the contrast agent in different phases of imaging by signal intensity (SI) and lesion contrast (C), to surrounding liver parenchyma, and comparing it across distinct groups of patients differentiated based on the histopathological grading of their HCC lesions and the presence of liver cirrhosis. Our results highlighted a significant contrast between well- and poorly-differentiated lesions regarding the lesion contrast in the arterial and late arterial phases. Furthermore, the hepatobiliary phase showed limited diagnostic value in cirrhotic liver parenchyma due to altered pharmacokinetics. Ultimately, our findings underscore the potential of Gd-EOB-DTPA-enhanced MRI as a tool for improving preoperative diagnosis and treatment selection for HCC while emphasizing the need for continued research to overcome the diagnostic complexities posed by the disease.

Publisher

MDPI AG

Reference52 articles.

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