Hepatocellular carcinoma in non-alcoholic steatohepatitis:Current knowledge and implications for management

被引:9
|
作者
George Cholankeril [1 ]
Ronak Patel [2 ]
Sandeep Khurana [3 ]
Sanjaya K Satapathy [1 ]
机构
[1] Division of Gastroenterology and Hepatology, Methodist University Hospital Transplant Institute, University of Tennessee Health Sciences Center
[2] Department of Medicine, University of Alabama at Birmingham, Montgomery Health Center
[3] Division of Gastroenterology, Georgia Regents University
关键词
Non-alcoholic steatohepatitis; Cirrhosis; Non-alcoholic fatty liver disease; Obesity; Hepatocellular carcinoma;
D O I
暂无
中图分类号
R575.5 [肝代谢障碍]; R735.7 [肝肿瘤];
学科分类号
1002 ; 100201 ; 100214 ;
摘要
With the prevalence of hepatitis C virus expected to decline, the proportion of hepatocellular carcinoma(HCC) related to non-alcoholic steatohepatitis(NASH) is anticipated to increase exponentially due to the growing epidemic of obesity and diabetes. The annual incidence rate of developing HCC in patients with NASH-related cirrhosis is not clearly understood with rates ranging from 2.6%-12.8%. While multiple new mechanisms have been implicated in the development of HCC in NASH; further prospective long-term studies are needed to validate these findings. Recent evidence has shown a significant proportion of patients with non-alcoholic fatty liver disease and NASH progress to HCC in the absence of cirrhosis. Liver resection and transplantation represent curative therapeutic options in select NASHrelated HCC patients but have placed a significant burden to our healthcare resources and utilization. Currently NASH-related HCC is the fastest growing indication for liver transplant in HCC candidates. Increased efforts to implement effective screening and preventative strategies, particularly in non-cirrhotic NASH patients, are needed to reduce the future impact imposed by NASH-related HCC.
引用
收藏
页码:533 / 543
页数:11
相关论文
共 50 条
  • [1] Non-Alcoholic Steatohepatitis and Hepatocellular Carcinoma: Implications for Lycopene Intervention
    Ip, Blanche C.
    Wang, Xiang-Dong
    NUTRIENTS, 2014, 6 (01) : 124 - 162
  • [2] Non-alcoholic Steatohepatitis (NASH) and Hepatocellular Carcinoma
    Antonio Cuadrado
    Aitor Orive
    Covadonga García-Suárez
    Agustín Domínguez
    Jose Carlos Fernández-Escalante
    Javier Crespo
    Fernando Pons-Romero
    Obesity Surgery, 2005, 15 : 442 - 446
  • [3] Non-alcoholic steatohepatitis and risk of hepatocellular carcinoma
    Rios, Rafael S.
    Zheng, Kenneth, I
    Zheng, Ming-Hua
    CHINESE MEDICAL JOURNAL, 2021, 134 (24) : 2911 - 2921
  • [4] Non-alcoholic steatohepatitis (NASH) and hepatocellular carcinoma
    Cuadrado, A
    Orive, A
    García-Suárez, C
    Domínguez, A
    Fernández-Escalante, JC
    Crespo, J
    Pons-Romero, F
    OBESITY SURGERY, 2005, 15 (03) : 442 - 446
  • [5] Non-alcoholic steatohepatitis and risk of hepatocellular carcinoma
    Rafael S. Rios
    Kenneth I. Zheng
    Ming-Hua Zheng
    中华医学杂志英文版, 2021, 134 (24) : 2911 - 2921
  • [6] Hepatocellular carcinoma in patients with non-alcoholic steatohepatitis
    Shimada, M
    Hashimoto, E
    Taniai, M
    Hasegawa, K
    Okuda, H
    Hayashi, N
    Takasaki, K
    Ludwig, J
    JOURNAL OF HEPATOLOGY, 2002, 37 (01) : 154 - 160
  • [7] Hepatocellular carcinoma arising in non-alcoholic steatohepatitis
    Zen, Y
    Katayanagi, K
    Tsuneyama, K
    Harada, K
    Araki, I
    Nakanuma, Y
    PATHOLOGY INTERNATIONAL, 2001, 51 (02) : 127 - 131
  • [8] Current management of non-alcoholic steatohepatitis
    Muthiah, Mark D.
    Sanyal, Arun J.
    LIVER INTERNATIONAL, 2020, 40 : 89 - 95
  • [9] Obesity and non-alcoholic steatohepatitis in immunotherapy for hepatocellular carcinoma
    Shuichiro Shiina
    Hitoshi Maruyama
    Maki Tobari
    Tatsuya Yamashita
    Hepatology International, 2023, 17 : 827 - 829
  • [10] Obesity and non-alcoholic steatohepatitis in immunotherapy for hepatocellular carcinoma
    Shiina, Shuichiro
    Maruyama, Hitoshi
    Tobari, Maki
    Yamashita, Tatsuya
    HEPATOLOGY INTERNATIONAL, 2023, 17 (04) : 827 - 829