Author/Authors :
Bronwyn Kerr، نويسنده , , William D. Foulkes، نويسنده , , D. Cade، نويسنده , , Ted L. Hadfield، نويسنده , , P. Hopwood، نويسنده , , Corinne Serruya، نويسنده , , E. Hoare، نويسنده , , Steven A. Narod، نويسنده , , D. Gareth Evans، نويسنده ,
Abstract :
Aims
Awareness of hereditary breast and ovarian cancer in both the general public and the medical profession is increasing. Individuals who may be at risk on the basis of a family history are requesting risk determination and appropriate management in a variety of settings. Risk determination relies largely on pedigree analysis and epidemiological data.
Methods
We describe five individuals presenting in the family cancer or genetic counselling clinic where a factitious family or personal history led to erroneous risk estimation. Common factors in these families are a history of benign breast disease, poor communication within families, long survival with early onset or bilateral disease, a lack of detailed knowledge of the illness and treatment in close relatives and inconsistencies in the history in repeated consultations.