Untreated liver observation on multiphase CT/MRI
Adult at high risk for HCC. No pathology proof. CT or MRI with extracellular contrast, or MRI with hepatobiliary contrast.
Liver Lesion Characterization (LI-RADS v2018): Untreated liver observation on multiphase CT/MRI → Do not use LI-RADS: under 18, vascular or congenital c...
Pathway Overview
21 steps
21 total
Adult at high risk for HCC. No pathology proof. CT or MRI with extracellular contrast, or MRI with hepatobiliary contrast.
In these patients LI-RADS is not validated. Benign nodules can look like HCC, so an LR-5 can be a false HCC diagnosis.
Cirrhosis, chronic hepatitis B, or current or prior HCC (includes adult liver transplant candidates and recipients). None of the exclusions above.
Not categorisable if image degradation or a missing phase prevents it.
Unequivocal enhancing soft tissue in a vein, with or without a visible mass. If unsure, it is not tumour in vein.
Multidisciplinary discussion for tailored workup. May include biopsy. Report: next to a targetoid mass, 'may be due to non-HCC malignancy'; next to an LR-5 mass, 'definitely due to HCC'; otherwise 'probably due to HCC'.
Examples: cyst, haemangioma, perfusion alteration (for example arterioportal shunt), focal fat deposition or sparing, hypertrophic pseudomass, confluent fibrosis or focal scar, spontaneous disappearance. A nodule that looks like FNH or hepatocellular adenoma is never LR-1: usually LR-3; LR-2 only with caution.
Return to surveillance in 6 months.
Probable forms of the benign entities above, or a distinctive solid nodule under 20 mm with no major feature and no LR-M feature, and either no ancillary feature of malignancy or ancillary features of both malignancy and benignity.
Return to surveillance in 6 months. Consider repeat diagnostic imaging in 6 months or less.
Targetoid mass (rim APHE, peripheral washout, delayed central enhancement, or targetoid diffusion restriction, transitional or hepatobiliary phase appearance). Or nontargetoid mass (no tumour in vein, not meeting LR-5) with infiltrative appearance, marked diffusion restriction, necrosis or severe ischaemia, or another feature of non-HCC malignancy. If unsure between LR-M and LR-4 or LR-5, choose LR-M.
Multidisciplinary discussion for tailored workup. Often includes biopsy. May be cholangiocarcinoma, combined HCC-cholangiocarcinoma, metastasis or atypical HCC.
Count a feature only when it is unequivocal. If unsure, count it as absent. Gadoxetate MRI: count washout only in the portal venous phase. Transitional or hepatobiliary phase hypointensity is not washout (ancillary feature only).
Category depends on APHE, size and the number of additional major features. LR-5 needs nonrim APHE and size 10 mm or more.
Ancillary features can never upgrade to LR-5. Distinctive nodule under 20 mm with no major feature: the ancillary feature of malignancy (with none of benignity) that excluded LR-2 gives LR-3. Do not upgrade it again.
Go to the one step below that matches the final category (LR-3, LR-4 or LR-5). Use the table category after any ancillary adjustment. If ancillary features downgrade LR-3 to LR-2: return to surveillance in 6 months; consider repeat diagnostic imaging in 6 months or less.
Repeat or alternative diagnostic imaging in 3 to 6 months.
Multidisciplinary discussion for tailored workup. May include biopsy.
Nonrim APHE, size 10 mm or more and the required major features. HCC is confirmed on imaging. Multidisciplinary discussion for consensus management.
Repeat or alternative diagnostic imaging in 3 months or less.
No HCC risk factor, under 18, cirrhosis from congenital hepatic fibrosis or a vascular disorder, or a path-proven lesion (report the pathology). Describe the observation and discuss with the hepatology or HCC team.
ACR CT/MRI LI-RADS v2018 Core (described in Chernyak et al., Radiology 2018)
Clinical Decision Support — Not a Substitute for Clinical Judgment
Individual patient factors may require deviation from these recommendations.
Known Limitations
Contraindicated Populations
Applicable Regions
AU: No Australian variant of LI-RADS. The ACR CT/MRI v2018 criteria apply. Follow the local HCC multidisciplinary team.
EU: EASL guidance uses its own non-invasive HCC criteria. Follow the local multidisciplinary team.
US: ACR LI-RADS CT/MRI v2018 is integrated into the AASLD 2018 HCC guidance. OPTN class 5A has adopted the LR-5 criteria.
APAC: Regional societies (for example APASL) use their own HCC imaging criteria. Follow the local multidisciplinary team.
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The Liver Lesion Characterization (LI-RADS v2018) is a diagnostic clinical algorithm for Radiology. It provides a structured decision tree to guide clinical decision-making, based on ACR CT/MRI LI-RADS v2018 Core (described in Chernyak et al., Radiology 2018).
This algorithm is based on ACR CT/MRI LI-RADS v2018 Core (described in Chernyak et al., Radiology 2018) (DOI: 10.1148/radiol.2018181494).
Known limitations include: CT/MRI LI-RADS only for adults at high risk for HCC (cirrhosis, chronic hepatitis B, current or prior HCC). Not for under 18, or cirrhosis from congenital hepatic fibrosis or a vascular disorder.; Does not cover treated observations (use LI-RADS CT/MRI treatment response v2024), CEUS LI-RADS or ultrasound surveillance.; Categories state imaging probability only. Final management needs multidisciplinary review of the whole patient.. Individual patient factors may require deviation from these recommendations.
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