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本文引用的文献

1
Hepatocellular carcinoma in long-term sustained virological responders following antiviral combination therapy for chronic hepatitis C.慢性丙型肝炎抗病毒联合治疗后长期持续病毒学应答者中的肝细胞癌
J Viral Hepat. 2008 Sep;15(9):659-65. doi: 10.1111/j.1365-2893.2008.01006.x. Epub 2008 Jul 10.
2
[Hepatocellular carcinoma in the non-cirrhotic liver].非肝硬化肝脏中的肝细胞癌
Pathologe. 2008 Feb;29(1):47-52. doi: 10.1007/s00292-007-0953-3.
3
Hepatic precancerous lesions and small hepatocellular carcinoma.肝癌前病变与小肝细胞癌
Gastroenterol Clin North Am. 2007 Dec;36(4):867-87, vii. doi: 10.1016/j.gtc.2007.08.010.
4
Liver enzyme flares and occult hepatitis B in persons with chronic hepatitis C infection.慢性丙型肝炎感染者的肝酶升高及隐匿性乙型肝炎
J Clin Virol. 2007 Jun;39(2):101-5. doi: 10.1016/j.jcv.2007.03.006. Epub 2007 Apr 23.
5
TP53 mutations and hepatocellular carcinoma: insights into the etiology and pathogenesis of liver cancer.TP53突变与肝细胞癌:对肝癌病因及发病机制的见解
Oncogene. 2007 Apr 2;26(15):2166-76. doi: 10.1038/sj.onc.1210279.
6
Hepatitis B virus integration, fragile sites, and hepatocarcinogenesis.乙型肝炎病毒整合、脆性位点与肝癌发生
Cancer Lett. 2007 Jul 18;252(2):157-70. doi: 10.1016/j.canlet.2006.11.010. Epub 2006 Dec 22.
7
Viral hepatitis and liver cancer: the case of hepatitis C.病毒性肝炎与肝癌:丙型肝炎病例
Oncogene. 2006 Jun 26;25(27):3834-47. doi: 10.1038/sj.onc.1209562.
8
The prevalence of hepatitis C virus infection in the United States, 1999 through 2002.1999年至2002年美国丙型肝炎病毒感染的流行情况。
Ann Intern Med. 2006 May 16;144(10):705-14. doi: 10.7326/0003-4819-144-10-200605160-00004.
9
Hepatocellular carcinoma: epidemiology, risk factors, and screening.肝细胞癌:流行病学、危险因素及筛查
Semin Liver Dis. 2005;25(2):143-54. doi: 10.1055/s-2005-871194.
10
Hepatitis C virus core protein stimulates hepatocyte growth: correlation with upregulation of wnt-1 expression.丙型肝炎病毒核心蛋白刺激肝细胞生长:与wnt-1表达上调的相关性。
Hepatology. 2005 May;41(5):1096-105. doi: 10.1002/hep.20668.

非肝硬化肝脏中的丙型肝炎相关肝细胞癌。

Hepatitis C-associated hepatocellular carcinomas in non-cirrhotic livers.

机构信息

Department of Pathology, University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

Mod Pathol. 2010 Feb;23(2):276-83. doi: 10.1038/modpathol.2009.174. Epub 2009 Nov 20.

DOI:10.1038/modpathol.2009.174
PMID:19935643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3037012/
Abstract

Chronic hepatitis C viral infection can lead to cirrhosis and hepatocellular carcinoma. It is generally believed that hepatitis C infection is not oncogeneic per se, but that the presence of cirrhosis determines the increased risk for hepatocellular carcinoma. However, a search of surgical pathology files from two large tertiary care centers for the years 2001-2008 identified a total of 18 hepatocellular carcinomas in non-cirrhotic livers with chronic hepatitis C infection. In six cases the background livers showed bridging fibrosis, while the remainder showed lower stages of fibrosis. Cases were negative for clinical and serological evidence of hepatitis B co-infection, and occult hepatitis B test was negative by PCR of formalin-fixed, paraffin embedded tissues. The tumors were also negative for TP53, exon 7, codon 249 mutations, a characteristic mutation strongly linked to aflatoxin exposure. The hepatocellular carcinomas had typical histology with no enrichment for unusual growth patterns or histological features. Among all resected hepatocellular carcinomas in non-cirrhotic livers over this time period, the prevalence of 16% with HCV infection was significantly greater than that expected by chance. In conclusion, these results demonstrate that hepatocellular carcinomas can arise in livers chronically infected with hepatitis C but without cirrhosis. These findings raise the possibility that in some cases hepatitis C infection and inflammation can be directly oncogeneic. It is also possible that established cirrhosis may have regressed in some cases. Regardless of the mechanism, these findings highlight an important and previously under-recognized risk for hepatocellular carcinoma in HCV-infected individuals who do not have cirrhosis.

摘要

慢性丙型肝炎病毒感染可导致肝硬化和肝细胞癌。一般认为,丙型肝炎感染本身并非致癌基因,但肝硬化的存在决定了肝细胞癌风险的增加。然而,在 2001 年至 2008 年间,对两个大型三级保健中心的外科病理学档案进行检索,共发现 18 例非肝硬化慢性丙型肝炎感染患者的肝细胞癌。在 6 例病例中,背景肝脏显示桥接纤维化,而其余病例显示较低阶段的纤维化。这些病例的临床和血清学乙型肝炎合并感染证据均为阴性,乙型肝炎隐匿性检测也为阴性(通过福尔马林固定石蜡包埋组织的 PCR 检测)。肿瘤也未检测到 TP53、外显子 7、密码子 249 突变,这种突变与黄曲霉毒素暴露密切相关。这些肝细胞癌具有典型的组织学特征,没有不寻常的生长模式或组织学特征的富集。在这段时间内,所有非肝硬化肝切除的肝细胞癌中,16%的病例与 HCV 感染相关,这一比例明显高于偶然预期。总之,这些结果表明,在没有肝硬化的情况下,丙型肝炎慢性感染的肝脏中也可能发生肝细胞癌。这些发现提示,在某些情况下,丙型肝炎感染和炎症可能直接致癌。也有可能在某些情况下,已确立的肝硬化已经消退。无论机制如何,这些发现突出了丙型肝炎感染个体中以前未被认识到的重要且以前被低估的肝细胞癌风险,这些个体没有肝硬化。