Multiple primary tumours in a population-based series of patients with histopathologically peer-reviewed sarcomas
Open Access
- 1 December 1993
- journal article
- Published by Springer Nature in British Journal of Cancer
- Vol. 68 (6) , 1243-1246
- https://doi.org/10.1038/bjc.1993.512
Abstract
Multiple primary tumours occurring in a three-year population-based series of patients with histopathologically peer-reviewed sarcomas from North West England were ascertained in order to look at the patterns of neoplasms seen. A total of 30 out of the 310 patients entered in the study had additional primary tumours. Very few patients were aged under 60 years at diagnosis of both their malignancies. The youngest was a known case of neurofibromatosis and, although seven patients were diagnosed with a sarcoma and carcinoma of the breast--a combination of cancers characteristic of the Li-Fraumeni cancer family syndrome--no other patients could directly be identified as suffering from any other cancer predisposition syndrome.Keywords
This publication has 13 references indexed in Scilit:
- Sarcomas in north west England: III SurvivalBritish Journal of Cancer, 1992
- p53 germline mutations in Li-Fraumeni syndromeThe Lancet, 1991
- Sarcomas in north west England: II IncidenceBritish Journal of Cancer, 1991
- Sarcomas in north west England: I. Histopathological peer reviewBritish Journal of Cancer, 1991
- Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other NeoplasmsScience, 1990
- A cancer family syndrome in twenty-four kindreds.1988
- CANCER IN SURVIVORS OF CHILDHOOD SOFT-TISSUE SARCOMA AND THEIR RELATIVES1987
- Soft-tissue and bone sarcoma histopathology peer review: the frequency of disagreement in diagnosis and the need for second pathology opinions. The Southeastern Cancer Study Group experience.Journal of Clinical Oncology, 1986
- Assessing completeness of cancer registration in the north-western region of England by a method of independent comparisonBritish Journal of Cancer, 1982
- Malignancy in neurofibromatosis.1981