A 66-year-old woman had a long-standing, scaly erythematous lesion on
her left temple which histologically showed features of amelanotic len
tigo maligna. It had recurred on numerous occasions over a period of 1
7 years, in spite of multiple attempts at curative surgery. There were
also recurrences within a skin graft which, to our knowledge, has not
been documented previously with lentigo maligna. In spite of the prol
onged course, and extensive intraepidermal melanocytic proliferation a
mounting to melanoma in situ, there has been no evidence of dermal inv
asion. The lack of pigmentation in such lesions means that clinical de
finition of margins is highly inaccurate. In view of the aggressive ho
rizontal growth phase of this lesion, with rapid recurrence following
surgery, it was treated with electron beam therapy, and this has resul
ted in complete clinical remission. This most unusual case illustrates
the potential difficulties in diagnosis and management of amelanotic
lentigo maligna.