MITF E318K: A rare homozygous case with multiple primary melanoma

Author:

Wallingford Courtney K.12,Maas Ellie J.1ORCID,Howard Antonia3,DeBortoli Emily13,Bhanja Deboshmita1,Lee Katie1,Mothershaw Adam1ORCID,Jagirdar Kasturee14,Willett Rod5,Betz‐Stablein Brigid1,Sturm Richard A.1,Soyer H. Peter12,McInerney‐Leo Aideen M.1

Affiliation:

1. Dermatology Research Centre Frazer Institute, The University of Queensland Brisbane Queensland Australia

2. Department of Dermatology Princess Alexandra Hospital Brisbane Queensland Australia

3. Graduate School of Health University of Technology Sydney Sydney Australia

4. Biochemistry and Molecular Biology Department Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

5. Jimboomba Junction Family Practice and Skin Cancer Clinic Jimboomba Queensland Australia

Abstract

AbstractMITF E318K moderates melanoma risk. Only five MITF E318K homozygous cases have been reported to date, one in association with melanoma. This novel report uses 3D total‐body‐photography (TBP) to describe the dermatological phenotype of a homozygous MITF E318K individual. The case, a 32‐year‐old male, was diagnosed with his first of six primary melanomas at 26 years of age. Five melanomas were located on the back and one in the groin. Two were superficial spreading. Three arose from pre‐existing naevi and one was a rare naevoid melanoma. 3D‐TBP revealed a high naevus count (n = 162) with pigmentation varying from light to dark. Most naevi generally (n = 90), and large (>5 mm diameter) and clinically atypical naevi specifically were located on the back where sun damage was mild. In contrast, naevi count was low (n = 25 total) on the head/neck and lower limbs where sun damage was severe. Thus, melanoma location correlated with naevi density, rather than degree of sun damage. In addition to the MITF E318K homozygosity, there was heterozygosity for four other moderate‐risk variants, which may contribute to melanoma risk. Further research is warranted to explore whether melanomas in E318K heterozygous and other homozygotes coincide with regions of high naevi density as opposed to sun damage. This could inform future melanoma screening/surveillance.

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

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