According to a recent study, multiple melanomas may be related to genetic factors. Dr. Jeannet J. Stam-Posthuma and his colleagues from Leiden University Medical Center in the Netherlands conducted a retrospective study on 56 melanoma patients to analyze the risk factors of the disease. These patients had a total of 157 melanomas. Of these patients, 64% had a family history of melanoma and 70.8% had a family history of dysplastic nevi. Eighty-two percent of the 50 patients examined had dysplastic nevi. Sixty percent of the patients had both clinically confirmed dysplastic nevi and a family history of melanoma. The mean age of patients at melanoma diagnosis was 38.2 years, and 58.9% of patients were younger than 40 years. The mean interval between the first and second melanoma resection was 34.3 months. In 76.8% of cases, the second melanoma was in a different anatomical site than the first tumor. Dr. Stam-Posthuma's team concluded, "The high incidence of dysplastic nevi in the patient and his family members, the high frequency of family history of melanoma, and the early onset of melanoma suggest that a genetic factor is involved in the development of multiple melanomas. Therefore, patients with one of these risk factors should be particularly careful." |
>>: Is melanoma a familial genetic disease?
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