Sorkin Tracy, Strautnieks Sandra, Foskett Pierre, Peddu Praveen, Thompson Richard J, Heaton Nigel, Quaglia Alberto
Histopathology Department, King's College Hospital, London, UK SE5 9RS.
Liver Molecular Genetics, King's College Hospital, London, UK SE5 9RS.
Hum Pathol. 2016 Jul;53:153-8. doi: 10.1016/j.humpath.2016.02.025. Epub 2016 Mar 30.
An 18-year-old man underwent liver transplantation due to an Abernethy malformation associated with multiple hepatocellular nodules including one which was rapidly enlarging and was suspicious for malignant transformation. Analysis of the explanted liver showed a spectrum of multiple hepatocellular nodules ranging in appearance from focal nodular hyperplasia, hepatocellular adenoma and to a well-differentiated hepatocellular neoplasm borderline for hepatocellular carcinoma. Mutational analysis revealed wild-type β-catenin expression in the background liver and some nodules, whilst different variants were present in other lesions irrespective of their morphological appearance. No telomerase reverse transcriptase (TERT) promoter mutation was identified. Abernethy malformations can lead to independent genetic events which can result in β-catenin mutations associated with malignant transformation of hepatocellular nodules. When following up such patients, one must therefore have a high index of suspicion, particularly if radiological surveillance reveals a change in the nature of hepatic lesions.
一名18岁男性因阿伯内西畸形伴多个肝细胞结节接受肝移植,其中一个结节迅速增大,怀疑发生恶变。对切除肝脏的分析显示有一系列多个肝细胞结节,其外观从局灶性结节性增生、肝细胞腺瘤到肝细胞癌边缘的高分化肝细胞肿瘤不等。突变分析显示,背景肝脏和一些结节中β-连环蛋白表达为野生型,而其他病变中存在不同变体,与它们的形态外观无关。未发现端粒酶逆转录酶(TERT)启动子突变。阿伯内西畸形可导致独立的基因事件,从而导致与肝细胞结节恶变相关的β-连环蛋白突变。因此,在对这类患者进行随访时,必须保持高度怀疑,尤其是当影像学监测显示肝脏病变性质发生变化时。