Hepatocellular adenoma in the paediatric population: Molecular classification and clinical associations

被引:12
作者
Hahn, Elan [1 ,2 ]
Putra, Juan [1 ,2 ]
机构
[1] Hosp Sick Children, Div Pathol, Dept Paediat Lab Med, 555 Univ Ave Room 3119, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5S 1A8, Canada
关键词
Paediatric; Hepatocellular adenoma; Malignant transformation; Beta-catenin; HNF1A; Glycogen storage disorders; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL PORTOSYSTEMIC SHUNTS; DISEASE TYPE-I; LIVER-TUMORS; MALIGNANT-TRANSFORMATION; HEPATIC ADENOMA; FANCONI-ANEMIA; NUCLEAR FACTOR; ACTIVATING MUTATIONS; CATENIN ACTIVATION;
D O I
10.3748/wjg.v26.i19.2294
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular adenomas (HCAs) represent rare, benign liver tumours occurring predominantly in females taking oral contraceptives. In children, HCAs comprise less than 5% of hepatic tumours and demonstrate association with various conditions. The contemporary classification of HCAs, based on their distinctive genotypes and clinical phenotypes, includeshepatocyte nuclear factor 1 homeobox alpha-inactivated HCAs,beta-catenin-mutated HCAs, inflammatory HCAs, combinedbeta-catenin-mutated and inflammatory HCAs, sonic hedgehog-activated HCAs, and unclassified HCAs. In children, there is a lack of literature on the characteristics and distribution of HCA subtypes. In this review, we summarized different HCA subtypes and the clinicopathologic spectrum of HCAs in the paediatric population.
引用
收藏
页码:2294 / 2304
页数:11
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