Risk of hepatoblastoma in familial adenomatous polyposis
- 1 August 1992
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 43 (6) , 1023-1025
- https://doi.org/10.1002/ajmg.1320430621
Abstract
Infantile and childhood hepatoblastoma occurs more frequently in persons heterozygous for the familial adenomatous polyposis (FAP) gene than in the general population. This observation is based on numerous case reports plus the results of an international survey of FAP registries. However, the frequency of this rare tumor in FAP patients is unknown. In a retrospective review of our family history data, 2/470 (0.42%) children born to 241 patients with FAP had hepatoblastoma. This figure is significantly higher than the 1/100,000 incidence of hepatoblastoma in the general population. However, for genetic counseling purposes, an empiric risk of <1% for hepatoblastoma can be cited to persons with FAP for their children.Keywords
This publication has 12 references indexed in Scilit:
- Brain tumors in familial adenomatous polyposisDiseases of the Colon & Rectum, 1989
- Hepatoblastoma and polyposis coli (familial adenomatous polyposis)Medical and Pediatric Oncology, 1989
- Hepatoblastoma and Familial Adenomatous PolyposisJNCI Journal of the National Cancer Institute, 1988
- Hepatoblastoma, pigmented ocular fundus lesions and jaw lesions in gardner syndromeAmerican Journal of Medical Genetics, 1988
- Adenomatous polyposis: An association with carcinoma of the thyroidBritish Journal of Surgery, 1987
- HepatoblastomaPublished by Springer Nature ,1987
- Hepatoblastoma and hepatocarcinoma in children: Analysis of a series of 29 casesJournal of Pediatric Surgery, 1986
- Association between hepatoblastoma and polyposis coli.Archives of Disease in Childhood, 1983
- Hepatocellular carcinoma associated with familial polyposis of the colonDiseases of the Colon & Rectum, 1983