Annals of Internal Medicine · 1969 · 1.5K citations · 20 references
MedicineGeneticsOncologyCancer GeneticsHuman GeneticsNeoplasiaFamilial Cancer AggregationHereditary Cancer SyndromesMalignant NeoplasmsPediatric SarcomasPediatric TumorsSoft Tissue SarcomasCancer Susceptibility SyndromesFamilial Cancer RiskFamilial Cancer SyndromesFamilial SyndromesMalignant Soft Tissue NeoplasmsNeoplastic DiseasePediatric Soft Tissue TumorsPrimary Neoplasms
Four families were identified in which a pair of children had soft-tissue sarcomas: three sets of sibs and one set of cousins. One parent of each affected child developed cancer; carcinoma of the breast occurred in three mothers under 30 years of age. Other young adults in these families had a high frequency of cancer, with no evidence of underlying genetic disorders known to carry a high risk of neoplasia. The increased familial susceptibility to cancer was manifested not only by the large number of members affected but by a seeming excess of multiple primary neoplasms. These findings suggest a new "familial" syndrome of neoplastic diseases in which heredity or oncogenic agents, or both, may have a causal role.
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