| Literature DB >> 6339032 |
S Schifter, L Vendelbo, O M Jensen, S Kaae.
Abstract
Retinoblastoma is found in a hereditary and nonhereditary form. Long survivors treated for the hereditary form seem to be predisposed for developing a second primary tumor later in life. The retinoblastoma genes are supposed to be responsible for this disposition. This report describes the development of a Ewing's tumor in a nine-year-old girl, who had both eyes removed in early life for retinoblastoma.Entities:
Mesh:
Year: 1983 PMID: 6339032 DOI: 10.1002/1097-0142(19830501)51:9<1746::aid-cncr2820510930>3.0.co;2-g
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860