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Liver cancer with concomitant TP53 and CTNNB1 mutations: a case report
Authors:Juliane Friemel  Markus Rechsteiner  Marion Bawohl  Lukas Frick  Beat Müllhaupt  Mickaël Lesurtel  Achim Weber
Affiliation:1.Institute of Surgical Pathology, University and University Hospital Zurich,Zurich,Switzerland;2.Leibniz Institute for Prevention Research and Epidemiology (BIPS),Bremen,Germany;3.Clinics of Hepatology and Gastroenterology, University and University Hospital Zurich,Zurich,Switzerland;4.Swiss Hepato-Pancreato-Biliary Center, Department of Digestive and Transplant Surgery,University Hospital of Zurich,Zurich,Switzerland
Abstract:

Background

In the spectrum of molecular alterations found in hepatocellular carcinoma (HCC), somatic mutations in the WNT/β-catenin pathway and the p53/cell cycle control pathway are among the most frequent ones. It has been suggested that both mutations occur in a mutually exclusive manner and they are used as molecular classifiers in HCC classification proposals.

Case presentation

Here, we report the case of a treatment-naïve mixed hepatocellular/cholangiocellular carcinoma (HCC/CCC) with morphological and genetic intratumor heterogeneity. Within the predominant part of the tumor with hepatocellular differentiation, a p.D32V mutation in exon 3 of the CTNNB1 gene occurred concomitantly with a TP53 intron 7/exon 8 splice site mutation.

Conclusion

Intratumor heterogeneity challenges the concept of CTNNB1 and TP53 gene mutations being mutually exclusive molecular classifiers in HCC, which has implications for HCC classification approaches.
Keywords:
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