青少年晚期肝细胞癌合并先天性胆汁淤积症：病例报告
Advanced hepatocellular carcinoma in adolescence associated with congenital cholestasis: a case description.
作者信息
Ladekarl Morten, Villadsen Gerda Elisabeth, Rudbeck Anne Roed, Aagenæs Oystein, Nielsen Jens Erik, Hamilton-Dutoit Stephen, Nordsmark Marianne
机构信息
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark, Norway.
出版信息
Case Rep Oncol. 2013 Feb 19;6(1):98-103. doi: 10.1159/000348715. Print 2013 Jan.
This case describes the clinical course and treatment of a 17-year-old male patient with advanced hepatocellular carcinoma (HCC) arising in a non-cirrhotic liver. The disease was thought to be caused by a congenital cholestatic syndrome associated with intermittent oedema in childhood, resembling the rare Aagenaes syndrome. Treatment choices in advanced HCC arising in adolescence are discussed.
本病例描述了一名17岁男性患者的临床病程及治疗情况，该患者患有非肝硬化肝脏中发生的晚期肝细胞癌（HCC）。该疾病被认为是由一种先天性胆汁淤积综合征引起的，该综合征在儿童期伴有间歇性水肿，类似于罕见的阿格内斯综合征。文中讨论了青少年晚期肝细胞癌的治疗选择。
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