Volume 59, Issue 3 pp. 362-365
Clinical Research Short Report

Increased risk of melanoma in C9ORF72 repeat expansion carriers: A case–control study

Miguel Tábuas-Pereira MD

Corresponding Author

Miguel Tábuas-Pereira MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

Faculty of Medicine, University of Coimbra, Portugal

These authors contributed equally to this study.

Correspondence to: M. Tábuas-Pereira; e-mail: [email protected]Search for more papers by this author
Luciano Almendra MD

Luciano Almendra MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

These authors contributed equally to this study.

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Maria Rosário Almeida MSC, PhD

Maria Rosário Almeida MSC, PhD

Centre for Neuroscience and Cell Biology, University of Coimbra, Portugal

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João Durães MD

João Durães MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

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André Pinho MD

André Pinho MD

Dermatology Department, Centro Hospitalar e Universitário de Coimbra, Portugal

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Anabela Matos MD

Anabela Matos MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

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Luis Negrão MD

Luis Negrão MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

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Argemiro Geraldo MD

Argemiro Geraldo MD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

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Isabel Santana MD, PhD

Isabel Santana MD, PhD

CHUC, Serviço de Neurologia, Praceta Prof. Mota Pinto, 3000-075, Coimbra, Portugal

Faculty of Medicine, University of Coimbra, Portugal

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First published: 17 November 2018
Citations: 3
Funding: Nothing to report.
Conflicts of Interest: None of the authors has any conflict of interest to disclose.

ABSTRACT

Introduction: Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are considered part of the same pathological spectrum. There is an increased risk of ALS in patients who have had melanoma. The risk of FTLD in melanoma (or cancer) patients is unknown. We aimed to study if C9ORF72 expansion is linked to a higher prevalence of melanoma. Methods: We selected patients with a diagnosis in the ALS-FTLD spectrum who were tested for pathogenic mutations. Medical history was reviewed, to identify those with pathologically documented melanomas. Results: We included 189 patients. Sixty-two had identified pathogenic mutations (39 C9ORF72). C9ORF72 carriers had a significantly higher risk of melanoma (odds ratio = 24.709; P < 0.007). There was no association with phenotype. Conclusions: These findings suggest that patients with a history of melanoma may have an increased probability of carrying a C9ORF72 repeat expansion. ALS or FTLD carriers of C9ORF72 should undergo surveillance for skin changes. Muscle Nerve 59:362–365, 2019

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