Hepatocellular Carcinoma in a 24-Year-Old Female with Beckwith-Wiedemann Syndrome: A Case Report and Review of the Literature.

Case Reports in Genetics Pub Date : 2020-10-07 eCollection Date: 2020-01-01 DOI:10.1155/2020/8811296
Carolyn G Ahlers, Quoc-Huy Trinh, Martin Montenovo
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Abstract

In this report, the case of a 24-year-old female with Beckwith-Wiedemann Syndrome (BWS) who was diagnosed with well-differentiated hepatocellular carcinoma (HCC) is described. While BWS has been associated with childhood embryonal tumors, most commonly Wilms tumors and hepatoblastomas, this is the first case report to describe HCC in an adult with BWS. Although HCC typically occurs in elderly adults or those with underlying liver disease, in this case, we show that HCC can occur in a young adult with BWS without any underlying liver disease.

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一名 24 岁女性贝克维特-维德曼综合征患者的肝细胞癌:病例报告与文献综述。
本报告描述了一名 24 岁女性贝克维茨-韦德曼综合征(BWS)患者被诊断为分化良好的肝细胞癌(HCC)的病例。虽然贝克维德曼综合征与儿童胚胎肿瘤(最常见的是威尔姆斯肿瘤和肝母细胞瘤)有关,但这是首例描述贝克维德曼综合征成人 HCC 的病例报告。虽然 HCC 通常发生在老年人或有潜在肝病的人身上,但在本病例中,我们发现患有 BWS 的年轻成人在没有任何潜在肝病的情况下也可能发生 HCC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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