Liu Shu, Chan Kwok Wah, Wang Bingyuan, Qiao Liang
Department of Gastroenterology, The First Affiliated Hospital of China Medical University, Shenyang 110001, Liaoning Province, China.
Am J Gastroenterol. 2009 Oct;104(10):2617-24; quiz 2625. doi: 10.1038/ajg.2009.440. Epub 2009 Jul 28.
Fibrolamellar hepatocellular carcinoma (FHLCC) generally occurs in young individuals lacking a background of chronic liver disease and other risk factors for hepatocellular carcinoma. The clinical presentations of FLHCC are generally nonspecific, and the alpha-fetoprotein level is typically within the normal range in most cases. Imaging studies have a major role in clinical diagnosis, but pathology is the gold standard in confirming diagnosis. Pathological characteristics of FLHCC include the presence of tumor cells with a deeply eosinophilic cytoplasm and macronucleoli surrounded by abundant fibrous bands. The most effective treatment for FLHCC is aggressive surgical resection. This comprehensive literature review gives a full account of the clinical, pathological, and molecular features of FLHCC.
纤维板层型肝细胞癌(FHLCC)通常发生在没有慢性肝病背景及其他肝细胞癌危险因素的年轻人中。纤维板层型肝细胞癌的临床表现通常不具有特异性,且在大多数情况下,甲胎蛋白水平通常在正常范围内。影像学检查在临床诊断中起主要作用,但病理检查是确诊的金标准。纤维板层型肝细胞癌的病理特征包括存在细胞质嗜酸性深染且有大核仁的肿瘤细胞,周围有丰富的纤维带。纤维板层型肝细胞癌最有效的治疗方法是积极的手术切除。这篇综合性文献综述全面阐述了纤维板层型肝细胞癌的临床、病理和分子特征。