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Clinical, phenotypic and oncologic background differences in patients with sporadic, familial and multiple primary melanoma.

Created on 01 Nov 2026

Authors

Irene López-Riquelme, Silvestre Martínez-García, Marina Romero-Bravo, Miguel-Ángel Berciano-Guerrero

Published in

Anais brasileiros de dermatologia. Volume 101. Issue 6. Pages 501472. Oct 31, 2026. Epub Oct 31, 2026.

Abstract

Sporadic Melanoma (SM) refers to patients with a single melanoma and no family history. Multiple Primary Melanoma (MPM) includes individuals with two or more primary melanomas. Familial Melanoma (FM) is defined as melanoma occurring in two first-degree relatives, or in three or more affected family members of any degree. Previous studies describe distinct phenotypic and clinical profiles in each subgroup, and a high proportion of personal and familial cancer history in patients with melanoma.
To compare phenotype, clinicopathological features, and oncological history in the three groups.
Data from 442 patients were collected and divided into three groups: FM, MPM, and SM.
The MPM group showed light eye color (p = 0.01), more tan 50 nevi (p = 0.00014), actinic keratoses (p = 0.0025), and melanomas arising from pre-existing nevi (p = 0.0031). FM patients were younger (p = 0.01) and had a higher burden of personal and family cancer history, particularly breast neoplasms (p = 0.01). SM presented ≥ 2 mitoses (p ≤ 0.0001). Multivariate analysis confirmed independent associations specific to each group.
Long term-follow-up for secondary melanoma is needed for validation. Also, some participants may not recall certain family history.
Patients with MPM display fair phototypes, numerous nevi, and markers of chronic sun damage, suggesting a central role of phenotype and cumulative UV exposure. In FM, younger age and a higher burden of oncologic history point toward an underlying genetic predisposition. SM is characterized by fewer nevi and aggressive melanomas, reflecting a distinct biological entity. These findings highlight the complex interplay between genetic and environmental factors.

PMID:
42966279
Bibliographic data and abstract were imported from PubMed on 01 Nov 2026.

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