Teaching non-specialist health care professionals how to identify the atypical mole syndrome phenotype: a multinational study
- 1 February 2000
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 142 (2) , 331-337
- https://doi.org/10.1046/j.1365-2133.2000.03405.x
Abstract
The atypical mole syndrome (AMS) phenotype is the strongest known risk factor for cutaneous melanoma but recognition of the phenotype has been claimed to be problematic and to require specialist assessment. This study determined the ability of previously unskilled doctors and nurses in five countries to recognize the phenotype after brief training. The system used was the AMS scoring system. This incorporates melanocytic naevus counts, clinical atypia of naevi and distribution of naevi. The agreement in scoring between the dermatologist and trained personnel was determined in 986 patients; overall agreement in diagnosis was 94.5% (kappa 0.70, P < 0.0001). The kappa scores in different countries ranged from 0.65 to 0.77 for individual naevus characteristics, indicative of good agreement. Accurate diagnosis of the atypical mole syndrome phenotype is possible by non-specialists. This has implications for collaborative studies of naevi, for screening and for both primary and secondary prevention of melanomaKeywords
This publication has 15 references indexed in Scilit:
- Family studies in melanoma: identification of the atypical mole syndrome (AMS) phenotypeMelanoma Research, 1994
- How common is the atypical mole syndrome phenotype in apparently sporadic melanoma?Journal of the American Academy of Dermatology, 1993
- Familial melanomaClinical and Experimental Dermatology, 1993
- The Dutch FAMMM family material: Clinical and genetic dataCytogenetic and Genome Research, 1992
- Genetic analysis of nevus density in melanoma familiesCytogenetic and Genome Research, 1992
- Prevalence of common and dysplastic naevi in a Swedish populationBritish Journal of Dermatology, 1991
- Mapping the Gene for Hereditary Cutaneous Malignant Melanoma–Dysplastic Nevus to Chromosome LpNew England Journal of Medicine, 1989
- Benign melanocytic naevi as a risk factor for malignant melanoma.BMJ, 1986
- Origin of familial malignant melanomas from heritable melanocytic lesions. 'The B-K mole syndrome'Archives of Dermatology, 1978