At-risk populations for osteosarcoma: the syndromes and beyond
- PMID: 22550413
- PMCID: PMC3329649
- DOI: 10.1155/2012/152382
At-risk populations for osteosarcoma: the syndromes and beyond
Abstract
Osteosarcoma is the most common primary malignancy of bone. Most cases are sporadic without a known genetic or environmental cause. Heritable genetic predisposition syndromes are associated with a small percentage of osteosarcomas. Study of these rare disorders has provided insight into the molecular pathogenesis of osteosarcoma. Screening of at-risk families and surveillance of affected individuals for these syndromes may permit earlier diagnosis and more effective treatment of osteosarcoma in these populations. This paper reviews the genetic and clinical features of the known osteosarcoma predisposition syndromes.
References
-
- Hauben EI, Arends J, Vandenbroucke JP, van Asperen CJ, Van Marck E, Hogendoorn PCW. Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma. European Journal of Human Genetics. 2003;11(8):611–618. - PubMed
-
- Ji J, Hemminki K. Familial risk for histology-specific bone cancers: an updated study in Sweden. European Journal of Cancer. 2006;42(14):2343–2349. - PubMed
-
- Li FP, Fraumeni JF. Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? Annals of Internal Medicine. 1969;71(4):747–752. - PubMed
