新生儿肝炎后肝细胞癌。

L. Moore, A. J. Bourne, BS David Moore, BS Henry Preston, BS Roger Byard
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引用次数: 17

摘要

肝细胞癌是一种罕见的恶性肿瘤,发生于幼儿,与多种先天性和后天疾病有关。人们普遍认为,特发性新生儿肝炎不是儿童时期肝细胞瘤的前兆。我们报告了一个28个月大的女婴,在4个月大时通过肝活检证实了新生儿巨细胞肝炎的诊断,并进行了一系列肝活检。乙型和丙型肝炎病毒感染和代谢异常已通过适当的检测排除。没有肠外营养史。在23个月大时进行的肝活检满足肝硬化诊断的形态学标准。在28个月时,由于持续的黄疸和腹部肿块的发展,进行了剖腹手术。肿块活检显示为肝细胞癌。倍性研究显示为非整倍体肿瘤,染色体分析证实为超二倍体核型。本病例通过连续活检证实了新生儿肝炎到肝硬化和肝细胞癌的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatocellular carcinoma following neonatal hepatitis.
Hepatocellular carcinoma is an uncommon malignancy in young children associated with a variety of congenital and acquired conditions. It has been generally held that idiopathic neonatal hepatitis is not an antecedent of hepatocellular neoplasia in childhood. We report a 28-month-old girl in whom a diagnosis of neonatal giant cell hepatitis was confirmed by liver biopsy at 4 months of age who was followed up with serial liver biopsies. Hepatitis B and C virus infection and metabolic abnormalities had been excluded by appropriate testing. There was no history of parenteral nutrition. The morphologic criteria for a diagnosis of cirrhosis were satisfied in a liver biopsy undertaken at 23 months of age. At 28 months a laparotomy was performed because of continuing jaundice and the development of an abdominal mass. Biopsy of the mass revealed a hepatocellular carcinoma. Ploidy studies showed an aneuploid tumor and a hyperdiploid karyotype was confirmed by chromosomal analysis. This case demonstrates by sequential biopsy the progression from neonatal hepatitis to cirrhosis and hepatocellular carcinoma in a young child.
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