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The incidence of adverse events (AEs) was 28.9% in the treatment group, with serious adverse events (SAEs) occurring in 26.3% of cases, showing no statistically significant difference compared to the control group

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Scarfi, and A.G.) with expertise in pigmented lesions and dermoscopy and no knowledge of the clinical history of the lesions independently analyzed the archived digital dermoscopic images and completed a printed questionnaire to categorize the lesions according to typical dermoscopic pattern analysis