Bronte Fabrizio, D'Amato Fabio, Barcellona Maria Rosa, Bronte Giuseppe, Malizia Giuseppe, Ialuna Salvatore, Fusco Giorgio, Verderame Francesco, Bronte Enrico, Bavetta Maria Grazia
Gastroenterology Unit, Ospedali Riuniti Villa Sofia - V. Cervello, Palermo, Italy.
Interventional Radiology and Neuroradiology Unit, Ospedali Riuniti Villa Sofia - V. Cervello, Palermo, Italy.
Cancer Rep (Hoboken). 2025 May;8(5):e70182. doi: 10.1002/cnr2.70182.
This case series aimed to explore the occurrence of synchronous hepatocellular carcinoma (HCC) and gastrointestinal adenocarcinoma in cirrhotic patients and to propose a potential common pathogenic mechanism.
We reviewed the available literature and retrospectively analyzed seven cases of cirrhotic patients with synchronous HCC and gastrointestinal adenocarcinoma (colon or gastric) identified in our center between March 2020 and June 2023. All patients underwent upper gastrointestinal endoscopy, abdominal ultrasound, computed tomography (CT) scan, and histological confirmation through biopsy or surgery. The mean age of the patients was 77.3 years (range 76-83), with five males and two females. Five patients had liver cirrhosis, and two had chronic hepatitis (one with HCV, one with MASLD). HCC was confirmed in all patients, with elevated alpha-fetoprotein levels (mean: 737.6 ng/mL). Colon adenocarcinoma was found in five patients, and gastric adenocarcinoma in one patient. Genetic and microsatellite instability analyses were performed in selected cases, revealing high microsatellite instability in one patient. We suggest that the Wnt/APC/β-catenin pathway might play a key role in the pathogenesis of both HCC and gastrointestinal malignancies.
Synchronous HCC and gastrointestinal adenocarcinoma may be increasingly identified due to prolonged survival in cirrhotic patients. Alterations in the Wnt/APC/β-catenin pathway could represent a shared pathogenic mechanism. Regular surveillance through ultrasound and endoscopy is essential for early diagnosis in this high-risk population. Future research is needed to confirm these findings and explore targeted treatments.
本病例系列旨在探讨肝硬化患者中同步发生肝细胞癌(HCC)和胃肠道腺癌的情况,并提出一种潜在的共同致病机制。
我们回顾了现有文献,并对2020年3月至2023年6月期间在本中心确诊的7例肝硬化患者同步发生HCC和胃肠道腺癌(结肠癌或胃癌)的病例进行了回顾性分析。所有患者均接受了上消化道内镜检查、腹部超声、计算机断层扫描(CT),并通过活检或手术进行了组织学确诊。患者的平均年龄为77.3岁(范围76 - 83岁),男性5例,女性2例。5例患者患有肝硬化,2例患有慢性肝炎(1例为丙型肝炎病毒感染,1例为代谢相关脂肪性肝病)。所有患者均确诊为HCC,甲胎蛋白水平升高(平均:737.6 ng/mL)。5例患者发现结肠癌,1例患者发现胃癌。对部分病例进行了基因和微卫星不稳定性分析,发现1例患者存在高微卫星不稳定性。我们认为Wnt/APC/β-连环蛋白通路可能在HCC和胃肠道恶性肿瘤的发病机制中起关键作用。
由于肝硬化患者生存期延长,同步发生的HCC和胃肠道腺癌可能会越来越多地被发现。Wnt/APC/β-连环蛋白通路的改变可能是一种共同的致病机制。通过超声和内镜进行定期监测对于这一高危人群的早期诊断至关重要。需要进一步的研究来证实这些发现并探索靶向治疗方法。