BPG is committed to discovery and dissemination of knowledge
Letter to the Editor
Copyright ©The Author(s) 2025.
World J Hepatol. Dec 27, 2025; 17(12): 115551
Published online Dec 27, 2025. doi: 10.4254/wjh.v17.i12.115551
Table 1 Comparative overview of imaging modalities utilized in preclinical hepatocellular carcinoma models
Imaging modality
Advantages
Limitations
Ref.
High-frequency ultrasound Real-time, non-invasive, affordable; enables serial monitoring and correlates well with histology or MRILimited soft-tissue contrast for small or heterogeneous lesions; accuracy may decrease for deep or poorly defined tumorsDevan et al[1], Roth et al[2], Molière et al[3]
HistologyGold standard for cellular detail; assessment of necrosis, vessels and immune cellsRequires tissue harvest; terminal procedure; not suitable for longitudinal studiesHerrero de la Parte et al[5], Choi et al[10]
Micro computed tomographyHigh-resolution three dimensional anatomy and vasculature; volume quantificationInvolves radiation exposure and need for contrast agents; limited soft-tissue contrastSingh et al[8], Cigliano et al[11]
MRIExcellent soft-tissue contrast; quantitative; reproducible; translationalExpensive; long scan time; limited accessibility in small animal settingsRojas et al[4], Renzulli and Giampalma[12]
Photoacoustic imagingCombines optical and ultrasound contrast to visualize vascular oxygenation and perfusionRestricted penetration depth; often relies on exogenous optical contrast agents; specialized setup required (operator dependent)Nyayapathi et al[7]
Super-resolution ultrasoundAllows visualization of microvascular changes beyond conventional resolutionRequires contrast microbubbles and operator dependent complex data processing; limited availability and standardizationHoyt[6], Riberdy et al[9]