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Mass Cytometry Analysis of Systemic and Local Immune Responses in Hepatocellular Carcinoma
Published on: April 25, 2025
868
A Limited Immunohistochemical Panel Can Subtype Hepatocellular Adenomas for Routine Practice
1From the Department of Pathology, Keck School of Medicine of the University of Southern California, Los Angeles.
American Journal of Clinical Pathology
|May 5, 2017
Summary
Immunohistochemistry readily identifies inflammatory and beta-catenin-activated adenomas, which carry a risk of cancer. This study confirms the necessity of immunostains for accurate subclassification of hepatocellular adenomas.
Area of Science:
- Hepatobiliary pathology
- Gastrointestinal pathology
- Oncology
Background:
- Hepatocellular adenomas with beta-catenin activation or inflammation have increased malignant transformation risk.
- These subtypes benefit from surgical excision.
- Accurate identification is crucial for patient management.
Purpose of the Study:
- To assess if a limited immunohistochemical panel can identify beta-catenin-activated and inflammatory adenomas.
- To determine the diagnostic accuracy of morphology versus immunohistochemistry for adenoma subclassification.
Main Methods:
- Morphological assessment of 46 adenomas.
- Immunohistochemical staining for beta-catenin, serum amyloid A, and glutamine synthetase.
- Comparison of morphologic diagnosis with final immunohistochemical results.
Main Results:
- Morphology alone yielded inaccurate subclassification in 43% of cases.
- Immunohistochemistry confirmed the diagnosis in 33% and changed it in 43% of cases.
- Final classification included inflammatory adenomas (35%), beta-catenin-activated adenomas (9%), beta-catenin-activated inflammatory adenomas (15%), and other adenomas (41%).
Conclusions:
- Immunohistochemistry effectively identifies inflammatory and beta-catenin-activated adenomas.
- Morphological assessment alone is insufficient for accurate adenoma subclassification.
- A limited panel of widely available immunostains enables accurate diagnosis of these high-risk adenoma subtypes.
Keywords:
Amyloid AGlutamine synthetaseHepatocellular adenomaHepatocellular carcinomaImmunohistochemistryInflammatory adenomaLiver diseaseLiver surgeryLiver tumorβ-Catenin
