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一名患有家族性罗素-西尔弗综合征儿童的肝细胞癌

Hepatocellular carcinoma in a child with familial Russell-Silver syndrome.

作者信息

Chitayat D, Friedman J M, Anderson L, Dimmick J E

机构信息

University of British Columbia Clinical Genetics Unit, Grace Hospital, Vancouver, B.C., Canada.

出版信息

Am J Med Genet. 1988 Dec;31(4):909-14. doi: 10.1002/ajmg.1320310425.

Abstract

We describe a 4-year-old boy with Russell-Silver syndrome (RSS) found to have hepatocellular carcinoma. The brother of this child also had manifestations of RSS. This is the third malignancy and the first hepatocellular carcinoma described in a patient with RSS. The coexistence of hepatocellular carcinoma and RSS may be completely fortuitous; however, the known association of liver cancer with growth abnormality and hemihypertrophy, findings also present in RSS, suggest that these disorders may be related.

摘要

我们描述了一名患有罗素-西尔弗综合征(RSS)的4岁男孩,他被发现患有肝细胞癌。该患儿的兄弟也有RSS的表现。这是RSS患者中描述的第三例恶性肿瘤,也是首例肝细胞癌。肝细胞癌与RSS的共存可能完全是偶然的;然而,已知肝癌与生长异常和半侧肥大有关,而这些表现也见于RSS,这表明这些疾病可能存在关联。

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