Multiple cutaneous melanomas in a patient with Li-Fraumeni syndrome: A case report

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Authors: Monika Rimdeikaite, Tomas Petras Vileikis, Domantas Stundys
Cited by: 0
References: 18

Abstract

Li-Fraumeni syndrome (LFS) is a rare genetic condition associated with an increased predisposition to various malignancies due to a mutation in the TP53 tumour-suppressor gene. The typical LFS tumour spectrum includes osteosarcoma, soft tissue sarcoma, pre-menopausal breast cancer, brain tumours and adrenocortical carcinoma. Although melanoma is not a hallmark of LFS, sporadic cases have been described in the literature. This article reports a patient with genetically confirmed Li-Fraumeni syndrome carrying the pathogenic TP53 NM_000546.5: c.357delC (p.Lys120Serfs∗3) variant, who developed three primary cutaneous melanomas in addition to several classical LFS-associated malignancies. While cutaneous tumours are not part of the typical LFS spectrum, the increased risk of multiple malignancies in LFS patients underscores the importance of annual dermatological examinations.

Fields of Study & Subjects

Virus-based gene therapy research Cancer-related Molecular Pathways Poxvirus research and outbreaks

Publication details

Journal / source
Heliyon
Publisher
Elsevier BV
Volume
12
Issue
13
Pages
e45210–e45210
Publication date
16 July 2026
Language
EN