BACKGROUND. Incidence rates of cutaneous malignant melanoma (CMM) have been
increasing for decades among Caucasian populations worldwide. Multiple fac
tors identify persons at increased risk of CMM, including those with a fami
ly history of melanoma and those with atypical moles. Approximately 6-12% o
f melanomas are familial and approximately 12% of patients with familial me
lanoma have multiple primary melanomas.
OBJECTIVE. TO report a case of a patient with atypical moles and with 17 mu
ltiple primary melanomas. To review the literature on multiple primary mela
nomas as well as to review the genetics and treatment of melanoma.
CONCLUSION. Patients with numerous atypical moles and a family or personal
history of melanoma are at greatest risk for developing CMM. Patients from
this population tend to develop CMM approximately 10 years earlier than the
general population and have an increased risk for developing multiple prim
ary melanomas. Since genetic tests capable of detecting individuals with an
inherited susceptibility to CMM are not available, it is important to iden
tify those patients with an increased risk and monitor them closely with re
gular total-body examinations.