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. 2020 May 21;26(19):2294–2304. doi: 10.3748/wjg.v26.i19.2294

Table 1.

Clinicopathologic characteristics of different hepatocellular adenoma subtypes

HCA subtype Risk factors Specific clinical features Histologic features IHCs
HHCA HNF1A germline mutations, MODY type 3, microsatellite instability Hepatic adenomatosis Intralesional steatosis LFABP (absent/decreased)
IHCA Obesity, alcohol, glycogenosis Inflammatory syndrome Sinusoidal dilatation, inflammatory infiltrate CRP, SAA
bex3HCA Male, liver vascular disease, androgen therapy Frequent malignant transformation Pseudoacinar formation, mild nuclear atypia beta-catenin (nuclear staining), GS (diffuse and strong)
bex7,8HCA No specific risk factors No specific clinical features No specific features GS (weak, heterogeneous)
shHCA Obesity Symptomatic bleeding Intratumoural hemorrhage Prostaglandin D2 synthase
UHCA No specific risk factors No specific clinical features No specific features None

HCA: Hepatocellular adenoma; IHCs: Immunohistochemical stains; HNF1A: hepatocyte nuclear factor 1 homeobox alpha; HHCA: HNF1A-inactivated hepatocellular adenoma; IHCA: Inflammatory hepatocellular adenoma; bex3HCA: Beta-catenin-mutated hepatocellular adenoma (exon 3); bex7,8HCA: Beta-catenin-mutated hepatocellular adenoma (exon 7/8); shHCA: Sonic hedgehog-activated hepatocellular adenoma; UHCA: Unclassified hepatocellular adenoma; MODY: Maturity-onset diabetes of the young; LFABP: Liver fatty acid binding protein; CRP: C-reactive protein; SAA: Serum amyloid A; GS: Glutamine synthetase.