| Literature DB >> 708576 |
Abstract
A primary renal tumour of childhood with histological appearances different from the nephroblastoma is described. This neoplasm, predominantly seen in boys, has a tendency to metastasize to bone. Such metastases are considered to be rare in nephroblastoma and this aspect in studies of Wilms' tumour series is thought to be due, for the most part, to the inclusion of a particular bone-metastasizing tumour in the material.Entities:
Mesh:
Year: 1978 PMID: 708576 PMCID: PMC2009742 DOI: 10.1038/bjc.1978.226
Source DB: PubMed Journal: Br J Cancer ISSN: 0007-0920 Impact factor: 7.640