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PMID: 1447251 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A significant proportion of patients with osteosarcoma may belong to Li-Fraumeni cancer families.

The Journal of bone and joint surgery. British volume ·Vol. 74 ·No. 6 ·1992-11-00 ·Pages 883-6

Porter DE, Holden ST, Steel CM, Cohen BB, Wallace MR, Reid R

Abstract

We studied the pedigrees of 17 index patients with osteosarcoma, recording malignant disease and cause of death for first- and second-degree relatives. There were seven cancers and five cancer deaths per 2151.5 person-years in first-degree relatives of osteosarcoma patients under the age of 50 years, a significantly greater incidence than in an age- and sex-matched population group (p < 0.001). This excess of malignancy was largely due to two families which fulfilled the criteria for the Li-Fraumeni cancer family syndrome. Both of these families were shown to have the genetic alterations in the p53 gene which have been implicated in this syndrome. Our study suggests that orthopaedic surgeons seeing new cases of osteosarcoma should arrange screening for familial malignancy.

MeSH Terms
Adolescent Adult Aged Bone Neoplasms/genetics Child Child, Preschool Genes, p53 Humans Infant Middle Aged Osteosarcoma/genetics Pedigree Scotland Soft Tissue Neoplasms/genetics Syndrome
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Porter D E
MRC Human Genetics Unit, Western General Hospital, Edinburgh, Scotland.
Holden S T
Steel C M
Cohen B B
Wallace M R
Reid R
Article Info
Journal
The Journal of bone and joint surgery. British volume
Abbr.
J Bone Joint Surg Br
ISSN
0301-620X
Published
1992-11-00
Pages
883-6
Language
English
Region
England
NLM ID
0375355
Subset
IM
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