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. 2025 Jan 22;14(3):686.
doi: 10.3390/jcm14030686.

Age-Related Variations in Clinical, Histological, and Genetic Characteristics in Multiple and Familial Melanomas: A Study of 333 Patients

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Age-Related Variations in Clinical, Histological, and Genetic Characteristics in Multiple and Familial Melanomas: A Study of 333 Patients

Andrea Carugno et al. J Clin Med. .

Abstract

Background/Objectives: Melanoma is an aggressive cutaneous malignancy with a rising incidence. While most cases are sporadic, 5-10% are hereditary, especially in patients with multiple or familial melanomas. The aim of this study is to explore the epidemiological, clinical, histological, and genetic features of this class of patients to identify risk factors for better management and surveillance. Methods: Between 2021 and 2024, patients with multiple melanomas or a familial history of melanoma were recruited. Collected data included demographic, clinic-pathologic features, and genetic analyses. Results: Patients >60 years had a higher prevalence of multiple melanomas (>50%, p = 0.0002), while familial melanoma was more common in those <40 years (54.3%). UV exposure increased with age, while sunscreen use decreased (p = 0.0004). Younger patients showed the highest nevi counts (mean: 139.6) and density (p < 0.0001). Dermatologists more frequently detected subsequent melanomas in older patients (>60 years) (p = 0.001). Genetic testing and melanoma subtypes showed no significant age-related differences. Conclusions: melanoma can develop at any age, and early detection through regular screening is crucial. Older patients (>60 years) have a higher prevalence of multiple melanomas, influenced by UV exposure and genetics. Indeed, in our cohort, a history of sun exposure, sunburns, and tanning bed use emerged as key risk factors, particularly among older individuals. Genetic testing showed a 4.3% rate of pathogenic/likely pathogenic variants, mainly in CDKN2A. Family history and nevus burden are significant risk factors, highlighting the need for targeted surveillance in high-risk populations.

Keywords: CDKN2A; familiar melanoma; genetic; melanoma; multiple primary melanoma; risk factors.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Distribution of melanoma subtypes across age groups. The classification includes multiple melanomas (purple), familial melanomas (green), and combined multiple and familial melanomas (blue). Patients over 60 years of age exhibited a significantly higher prevalence of multiple melanomas compared to younger age groups, with more than half presenting with multiple lesions. In contrast, familial melanoma was more common among younger patients, with 54.3% of individuals under 40 years showing a familial pattern (p = 0.0002).
Figure 2
Figure 2
Distribution of melanoma patients according to UV exposure and prevention behaviors across age groups. (a) History of sunburns. (b) Occupational UV exposure. (c) Use of tanning beds. (d) Use of sunscreens. Older patients (>60 years) reported the highest levels of occupational and recreational UV exposure (19.7%, p = 0.005) and tanning bed use (81.7%, p < 0.0001), alongside significantly lower sunscreen use (35.2% reported no sunscreen use, p = 0.0004). In contrast, younger patients (<40 years) reported more frequent sunburns during both childhood and adulthood, while older patients reported more sunburns in adulthood (p = 0.01).

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References

    1. Karimkhani C., Green A.C., Nijsten T., Weinstock M.A., Dellavalle R.P., Naghavi M., Fitzmaurice C. The global burden of melanoma: Results from the Global Burden of Disease Study 2015. Br. J. Dermatol. 2017;177:134–140. doi: 10.1111/bjd.15510. - DOI - PMC - PubMed
    1. Paolino G., Podo Brunetti A., De Rosa C., Cantisani C., Rongioletti F., Carugno A., Zerbinati N., Valenti M., Mascagni D., Tosti G., et al. Anorectal melanoma: Systematic review of the current literature of an aggressive type of melanoma. Melanoma Res. 2024;34:487–496. doi: 10.1097/CMR.0000000000001003. - DOI - PMC - PubMed
    1. Wu X.C., Eide M.J., King J., Saraiya M., Huang Y., Wiggins C., Barnholtz-Sloan J.S., Martin N., Cokkinides V., Miller J., et al. Racial and ethnic variations in incidence and survival of cutaneous melanoma in the United States, 1999–2006. J. Am. Acad. Dermatol. 2011;65((Suppl. 1)):S26–S37. doi: 10.1016/j.jaad.2011.05.034. - DOI - PubMed
    1. Whiteman D.C., Green A.C., Olsen C.M. The Growing Burden of Invasive Melanoma: Projections of Incidence Rates and Numbers of New Cases in Six Susceptible Populations through 2031. J. Investig. Dermatol. 2016;136:1161–1171. doi: 10.1016/j.jid.2016.01.035. - DOI - PubMed
    1. Shaikh W.R., Dusza S.W., Weinstock M.A., Oliveria S.A., Geller A.C., Halpern A.C. Melanoma Thickness and Survival Trends in the United States, 1989 to 2009. J. Natl. Cancer Inst. 2015;108:djv294. doi: 10.1093/jnci/djv294. - DOI - PMC - PubMed

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