| Literature DB >> 22497519 |
Claudia Curchin1, Elisabeth Wurm, Kasturee Jagirdar, Richard Sturm, Peter Soyer.
Abstract
We present a case of an amelanotic nodular melanoma occurring in a 26-year-old woman who carried a heterozygous (melancortin-1-receptor) MC1R 160R/W and tyrosinase (TYR) 402R/Q genotype and had a dark hair phenotype. We present dermoscopic, reflectance confocal microscopy (RCM) and histopathological images of the melanoma. We discuss the relationship between MC1R red hair colour (RHC) variants, TYR variants, phenotype and melanoma development. We also discuss the merits of RCM as an additional diagnostic aid for equivocal melanocytic lesions.Entities:
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Year: 2012 PMID: 22497519 DOI: 10.1111/j.1440-0960.2012.00882.x
Source DB: PubMed Journal: Australas J Dermatol ISSN: 0004-8380 Impact factor: 2.875