Skip to main content

Unclassified hepatocellular adenoma with beta-catenin mutation: a case report



Hepatocellular adenoma (HCA) subtypes are considered as risk factors for malignant transformation; thus, an accurate diagnosis is important. We report a case of resected HCA previously diagnosed as unclassified HCA using immunohistochemistry, subsequently discovered to harbor a mutation in exon 3 of the beta (β)-catenin gene using deoxyribonucleic acid (DNA) sequencing.

Case presentation

The patient was a 26-year-old woman who was referred to our hospital because of a 150-mm tumor in the right lobe of the liver. Considering the possibility of malignancy, we performed right lobe hepatectomy. Based on the histopathological and immunohistochemical findings, the tumor was diagnosed as an unclassified HCA. Next, we performed sequencing of DNA isolated from the tumor and identified a mutation in exon 3 of β-catenin, suggesting that the tumor contained an activating mutation of the β-catenin gene.


β-Catenin mutations in HCA cannot be detected by immunohistochemistry alone, and molecular analysis is required to accurately diagnose and evaluate its prognosis.


Hepatocellular adenoma (HCA) is a rare, benign tumor of the liver, often observed in young women taking oral contraceptives, with an estimated incidence of 3 per 1,000,000 per year [1]. HCA is divided into four subtypes based on molecular and pathological features: hepatocyte nuclear factor 1 alpha (HNF1α)-mutated HCA (HHCA), inflammatory HCA (IHCA), β-catenin-mutated HCA (b-HCA), and unclassified HCA (UHCA) [2]. Immunohistochemical analysis usually shows a lack of liver fatty acid-binding protein (LFABP) in HHCA, serum amyloid A (SAA) and C-reactive protein (CRP) overexpression in IHCA, diffuse and strong glutamine synthetase (GS) expression and nuclear β-catenin in b-HCA, and no specific features in UHCA [3]. Because b-HCA is associated with a high risk of malignant transformation, accurate diagnosis of the subtype is important for evaluating its prognosis [4]. However, β-catenin mutation cannot be detected by immunohistochemical analysis alone [5].

Herein, we report a case of UHCA that was demonstrated to have β-catenin mutation and discuss the significance of the collaboration between immunohistochemistry and molecular analysis in the diagnosis of HCA.

Case presentation

The patient was a 26-year-old woman. She was admitted to our hospital because of a massive hepatic tumor, which was detected incidentally during investigations for hepatic disorders. She had no history of oral contraceptives. Hepatitis B virus surface antigen and hepatitis C virus antibody were both found to be negative. The patient’s blood tests showed aspartate aminotransferase, 26 U/L (normal range, 5–30 U/L); alanine phosphatase, 14 U/L (normal range, 10–30 U/L); gamma-glutamyl transpeptidase, 260 IU/L (normal range, 10–47 IU/L); total bilirubin, 0.7 mg/dL (normal range, mg/dL); carcinoembryonic antigen, 0.9 ng/mL (normal range, < 5.0 ng/mL); carbohydrate antigen 19–9, 9.0 U/mL (normal range, < 15 U/mL); alpha-fetoprotein, 1.1 ng/mL (normal range, < 15 ng/mL); and protein induced by vitamin K absence or antagonist II, 192 mAU/mL (normal range, < 15 mAU/mL). An indocyanine green retention rate at 15 min was 4.2% with Child–Pugh grade A. Enhanced computed tomography showed a 150-mm-diameter enhanced tumor on the right hepatic lobe (Fig. 1a, b), with a clear border between the tumor and the peripheral tissue. Gadolinium-enhanced magnetic resonance imaging also showed an enhanced tumor (Fig. 1c), with no intensity difference compared to the background liver in the diffusion-weighted images (Fig. 1d). 18F-fluorodeoxyglucose positron-emission tomography showed a slightly high 2-fluoro-2-deoxy-d-glucose uptake in the tumor (maximum standard unit value = 2.7) (Fig. 2). Based on these findings, we performed right lobe hepatectomy because malignancy, including hepatocellular carcinoma (HCC), could not be excluded. The tumor was yellowish-brown, with demarcating borders, measuring 155 × 140 mm (Fig. 3). Histopathological findings showed diffuse proliferation of the hepatocellular cells, with poor atypia (Fig. 4a). Although some tumor cells had doublet nuclei, no difference in nuclear size, nuclear chromatin, or karyomitosis was observed. Based on these findings, a diagnosis of hepatocellular adenoma was made. Immunohistochemical analysis was positive for membranous β-catenin, negative for nuclear β-catenin, diffusely positive for GS, positive for LFABP, and negative for SAA and CRP (Fig. 4b, c, d, e, f, respectively). The non-tumor tissue showed similar membranous β-catenin staining (Additional file 1: Figure S1). Based on these findings, the tumor was diagnosed as UHCA. Next, we extracted DNA from the tumor and non-tumor tissues using the DNeasy Blood and Tissue Kit (QIAGEN, Germany) and performed DNA polymerase chain reaction (PCR) using primers to amplify β-catenin (CTNNB1) exons 3, 7, and 8 (Table 1). The primers designs were referenced from Rebouissou et al. [6]. The primers of exon 3 were designed to detect sequences between exon 2 and exon 4. Electrophoresis of PCR products from exon 3 showed two different bands (No. 1 and No. 2) from the tumor and one band from non-tumor DNA (Fig. 5a). The same length bands were detected in exon 7 and 8 (Fig. 5a). We extracted the DNA from each gel, including the bands, and performed direct DNA sequencing. The amplicon of No. 1 band (approximately 530-bp) was detected only from the tumor tissue but not from the non-tumor tissue and showed a large deletion of 631 bp from the intron between exon 2 and exon 3 to exon 4 (Fig. 5b; The borderline indicates the deletion site.). Based on these results, we concluded that the tumor had a β-catenin mutation. The amplicon with a band around 1100 bp (No. 2) was considered to be contaminated from non-tumor tissue. There was no mutation in exon 7 and 8 of the tumor. According to these findings, the tumor was demonstrated to have a mutation that had a large deletion including the beta-transducin repeats-containing protein (β‐TrCP) binding site.

Fig. 1

Enhanced computed tomography (CT) and gadolinium ethoxybenzyl diethylenetriamine pentaacetic acid-enhanced MRI findings CT showed a 150-mm-diameter tumor in the right hepatic lobe: a axial view, b coronal view. MRI showed c. No high intensity is detected compared to the background liver in the diffusion-weighted images (d)

Fig. 2

18F-fluorodeoxyglucose positron-emission tomography (FDG-PET) finding. FDG-PET showed slightly high FDG uptake of the tumor (SUVmax = 2.7). FDG 2-fluoro-2-deoxy-d-glucose, SUVmax maximum standard unit value

Fig. 3

Photograph of the resected specimen. The tumor measuring 155 × 140 mm in the resected right lobe

Fig. 4

Histopathology and immunohistochemistry findings. Hepatocellular cells with poor atypia proliferated diffusely in the tumor (a) H&E staining (magnification, 200 ×). Immunohistochemical analysis shows positive β-catenin in the cellular membrane and negative in the nucleus (magnification, 200 ×) (b), diffuse GS (magnification, 200 ×) (c), LFABP is positive (magnification, 200 ×) (d), SAA is negative (magnification, 200 ×) (e), and CRP is negative (magnification, 200 ×) (f). H&E stain, hematoxylin and eosin staining; GS, glutamine synthase; LFABP, liver fatty acid-binding protein; SAA, serum amyloid A; CRP, C-reactive protein

Table 1 The primers list for exon 3, exon 7, and exon 8 of the catenin beta-1 gene
Fig. 5

PCR and direct DNA sequencing results. a Electrophoresis of PCR products for exon 3, exon 7, and exon 8 of the β-catenin gene in tumor and non-tumor tissues. Leftmost is a 100-bp DNA ladder (Takara Bio Inc., Shiga, Japan). The PCR products of exon 3 of the β-catenin gene amplified from tumor DNA show two different bands, while that from non-tumor DNA shows a single band. The same band length is detected in exon 7 and exon 8. b DNA sequencing of exons 3 shows a large deletion, including introns between exon 2 and exon 3 to exon 4. The deletion site is marked by the solid black vertical line. PCR, polymerase chain reaction; DNA, deoxyribonucleic acid

The postoperative course was good, and the patient was discharged 13 days after the surgery. No recurrence has been observed for 1 year.


UHCA accounts for 10% of all HCAs and has not been characterized by a specific phenotype, radiological features, or genetic mutations [7]. The significance of β-catenin mutation in UHCA has not been established.

B-HCA accounts for 7–14% of HCA and is characterized by activating mutations of the CTNNB1 gene [7]. Activating mutations can occur in exons 3, 7, or 8 of the CTNNB1 gene in HCC and HCA [8] and are found in 20–34% of HCCs, suggesting that β-catenin is the most frequently activated oncogene in HCC [9].

Several mutations have been identified in the CTNNB1 gene in HCA, leading to the activation of β‐catenin. Large in‐frame exon 3 deletions and point mutations occurring at the D32‐S37 residues cause a strong β‐catenin signal due to the direct disruption of the β‐TrCP binding site, consequently suppressing its ubiquitination and proteasomal degradation [8]. Male sex and β-catenin exon 3 mutations in b-HCA are significantly associated with a higher risk of malignant transformation [10]. Mutations located at the T41 amino acid residue show moderate activation, whereas mutations located at S45, K335, and N387 show weak activation of β‐catenin [6]. Mutations in exon 3 often show both homogeneous GS overexpression and nuclear β‐catenin accumulation [6]. Conversely, exon 3 S45, exon 7, and exon 8 mutations demonstrate only weak, heterogeneous GS expression without nuclear β‐catenin accumulation [11]. β-Catenin mutations are not associated with nuclear β-catenin staining, suggesting that some CTNNB1 alterations may not disrupt GS and β-catenin patterns.

In our patient, although the tumor had a large deletion of exon 3, including the β‐TrCP binding site, it did not show nuclear β-catenin staining, leading to UHCA diagnosis. Because both tumor and non-tumor sections showed similar membranous β-catenin staining, it was not suggested that the large deletion of CTNNB1 gene caused the loss of β-catenin antigenicity.

Regarding cases with discordance between GS and β-catenin staining, the tumors are speculated to have activation of an alternative pathway causing GS expression [4]. Austinat et al. reported a case of HCC that showed an expression of cytosolic β-catenin and GS, which was identified as a 3-bp deletion affecting the tyrosine at position 97 within the adenomatous polyposis coli protein-binding site of Axin1 [12]. Additionally, another study described strong GS staining in a peliotic HCA, suggesting that vascular flow alterations and hepatic parenchymal remodeling increased GS expression [13]. Therefore, aberrant GS expression can occur without β-catenin nuclear translocation.

Abnormal GS expression is considered to be a useful marker for b-HCA, even in the absence of aberrant nuclear β-catenin staining [14]. In HCC, GS immunostaining was reported to have better sensitivity and specificity than β‐catenin because β‐catenin antibody is often difficult to interpret due to weak staining and lower sensitivity [15, 16]. In cases with positive GS staining, molecular analysis is needed to detect β-catenin mutations. In this case because the tumor possibly includes a strong activation of β-catenin signaling, close follow-up is necessary based on the risk of recurrence.


We performed hepatectomy for HCA, and β-catenin mutation was detected using PCR and direct DNA sequencing. It is necessary to perform mutational analysis in cases with positive GS staining.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.



Hepatocellular adenoma


Hepatocyte nuclear factor 1 alpha-mutated HCA


Inflammatory HCA


β-Catenin-mutated hepatocellular adenoma


Unclassified hepatocellular adenoma


Liver fatty acid-binding protein


Serum amyloid A


C-reactive protein


Glutamine synthetase


Hepatocellular carcinoma


Deoxyribonucleic acid




Polymerase chain reaction


Beta-transducin repeats-containing proteins

H&E staining:

Hematoxylin and eosin staining


Magnetic resonance imaging


  1. 1.

    Barthelmes L, Tait IS. Liver cell adenoma and liver cell adenomatosis. HPB (Oxf). 2005;7:186–96.

    Article  Google Scholar 

  2. 2.

    Renzulli M, Clemente A, Tovoli F, Cappabianca S, Bolondi L, Golfieri R. Hepatocellular adenoma: an unsolved diagnostic enigma. World J Gastroenterol. 2019;25:2442–9.

    Article  Google Scholar 

  3. 3.

    Beaufrère A, Paradis V. Hepatocellular adenomas: review of pathological and molecular features. Hum Pathol. 2020.

    Article  PubMed  Google Scholar 

  4. 4.

    Krause K, Tanabe KK. A shifting paradigm in diagnosis and management of hepatic adenoma. Ann Surg Oncol. 2020;27:3330–8.

    Article  Google Scholar 

  5. 5.

    Margolskee E, Bao F, de Gonzalez AK, Moreira RK, Lagana S, Sireci AN, et al. Hepatocellular adenoma classification: a comparative evaluation of immunohistochemistry and targeted mutational analysis. Diagn Pathol. 2016;11:27.

    Article  Google Scholar 

  6. 6.

    Rebouissou S, Franconi A, Calderaro J, Letouzé E, Imbeaud S, Pilati C, et al. Genotype-phenotype correlation of CTNNB1 mutations reveals different ß-catenin activity associated with liver tumor progression. Hepatology. 2016;64:2047–61.

    CAS  Article  Google Scholar 

  7. 7.

    Hoshino K, Harimoto N, Muranushi R, Hagiwara K, Yamanaka T, Ishii N, et al. Unclassified hepatocellular adenoma with histological brown pigment deposition and serum Pivka-II level elevation: a case report. Surg Case Rep. 2020;6:94.

    Article  Google Scholar 

  8. 8.

    Nault JC, Couchy G, Balabaud C, Morcrette G, Caruso S, Blanc JF, et al. Molecular classification of hepatocellular adenoma associates with risk factors, bleeding, and malignant transformation. Gastroenterology. 2017;152(880–94):e6.

    Google Scholar 

  9. 9.

    Zucman-Rossi J, Jeannot E, Nhieu JT, Scoazec JY, Guettier C, Rebouissou S, et al. Genotype-phenotype correlation in hepatocellular adenoma: new classification and relationship with HCC. Hepatology. 2006;43:515–24.

    CAS  Article  Google Scholar 

  10. 10.

    Dokmak S, Paradis V, Vilgrain V, Sauvanet A, Farges O, Valla D, et al. A single-center surgical experience of 122 patients with single and multiple hepatocellular adenomas. Gastroenterology. 2009;137:1698–705.

    Article  Google Scholar 

  11. 11.

    Klompenhouwer AJ, de Man RA, Dioguardi Burgio M, Vilgrain V, Zucman-Rossi J, Ijzermans JNM. New insights in the management of hepatocellular adenoma. Liver Int. 2020;40:1529–37.

    Article  Google Scholar 

  12. 12.

    Austinat M, Dunsch R, Wittekind C, Tannapfel A, Gebhardt R, Gaunitz F. Correlation between beta-catenin mutations and expression of Wnt-signaling target genes in hepatocellular carcinoma. Mol Cancer. 2008;7:21.

    Article  Google Scholar 

  13. 13.

    Berry RS, Gullapalli RR, Wu J, Morris K, Hanson JA. Diffuse glutamine synthetase overexpression restricted to areas of peliosis in a β-catenin-activated hepatocellular adenoma: a potential pitfall in glutamine synthetase interpretation. Virchows Arch. 2014;465:241–5.

    CAS  Article  Google Scholar 

  14. 14.

    Bioulac-Sage P, Taouji S, Le Bail B, Possenti L, Balabaud C. Value and limits of routine histology alone or combined with glutamine synthetase immunostaining in the diagnosis of hepatocellular adenoma subtypes on surgical specimens. Int J Hepatol. 2013;2013:1–8.

    Google Scholar 

  15. 15.

    Audard V, Grimber G, Elie C, Radenen B, Audebourg A, Letourneur F, et al. Cholestasis is a marker for hepatocellular carcinomas displaying beta-catenin mutations. J Pathol. 2007;212:345–52.

    CAS  Article  Google Scholar 

  16. 16.

    Hale G, Liu X, Hu J, Xu Z, Che L, Solomon D, et al. Correlation of exon 3 β-catenin mutations with glutamine synthetase staining patterns in hepatocellular adenoma and hepatocellular carcinoma. Mod Pathol. 2016;29:1370–80.

    CAS  Article  Google Scholar 

Download references


We would like to thank Editage ( for English language editing.


No grant support or funding from public institutions or private enterprises was received for this case report.

Author information




RM performed DNA sequencing and wrote the manuscript. KA, NH, TY, KH, KH, NI, MT, TI, AW, and NK were involved in treating the patient and helped draft the manuscript. SA diagnosed the pathological findings. KS participated in critically revising the manuscript. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Norifumi Harimoto.

Ethics declarations

Ethics approval and consent to participate

This case report was performed in accordance with the Declaration of Helsinki, and patients granted their written informed consent to participate in this study according to our institutional consent form.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and the accompanying images.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Figure S1.

Immunohistochemistry findings of β-catenin in non-tumor tissue. β-Catenin is positive in the cellular membrane and negative in the nucleus.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Muranushi, R., Araki, K., Harimoto, N. et al. Unclassified hepatocellular adenoma with beta-catenin mutation: a case report. surg case rep 7, 46 (2021).

Download citation


  • Hepatocellular adenoma
  • β-Catenin mutation
  • Hepatectomy