Actinic keratoses (AKs) are focal areas of dysplasia with low risk of
progression to squamous cell cancer; many regress spontaneously. Using
polymerase-chain-reaction microsatellite analysis, we found that loss
of heterozygosity on several chromosome arms, including 17p, 17q, 9p,
9q, and 13q, was common in AKs. More than half the AKs examined showe
d loss of heterozygosity at four or more loci. The apparent genetic in
stability of these lesions contrasts with their benign clinical course
.