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Clinicopathologically Defined Nevus Subtypes and Melanoma Risk
Veronique Clauwaert1, Evelien Verhaeghe2, Sofie De Schepper2
1Dermpat, Ghent, Oost-Vlaanderen, Belgium; Dermatology Department, Ghent University Hospital, Ghent, Oost-Vlaanderen, Belgium.
The Journal of Investigative Dermatology
|June 28, 2024
Summary
Nearly half of excised nevi are hypermelanotic subtypes with low melanoma risk, suggesting overtreatment. Atypical lentiginous and orange pulverocytic flat nevi subtypes show higher melanoma risk and atypia, warranting further research.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Early melanoma detection significantly impacts patient outcomes and influences clinical nevus excision rates.
- Understanding nevus subtypes is crucial for accurate risk assessment and optimizing clinical management.
Purpose of the Study:
- To evaluate demographic characteristics and melanoma risk associated with clinically suspicious, primarily flat nevus subtypes.
- To identify specific nevus subtypes that may indicate increased melanoma risk.
Main Methods:
- Analysis of over 7000 excised nevi using ex vivo dermoscopy and derm dotting to identify 12 prevalent subtypes.
- Detailed description of dermoscopic, histopathological, and clinical features for each subtype.
- Comparison of nevus subtypes regarding melanoma history, histopathological atypia, and in-situ melanoma occurrence.
Main Results:
- The hypermelanotic nevus subtype constituted nearly half of excised nevi, exhibiting mild atypia and low melanoma association, suggesting potential overtreatment.
- Atypical lentiginous nevus and orange pulverocytic flat nevus subtypes were linked to increased rates of severe atypia and melanoma history.
- Significant variations in melanoma risk and histopathological atypia were observed across different nevus subtypes.
Conclusions:
- Certain nevus subtypes, like atypical lentiginous and orange pulverocytic flat nevi, are associated with higher melanoma risk and atypia.
- Findings suggest these subtypes may represent distinct genetic or tumoral entities influencing melanoma development.
- Further prospective research on specific nevus subtypes is recommended to elucidate clinical/genetic factors and refine melanoma risk assessment.

