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  • Presentation

Dysplastic Nevi: Diagnostic Challenges, Management Controversies, and Clinical Decision-Making

Description

The talk explains that managing dysplastic nevi is challenging because their malignant potential is uncertain, histologic grading is subjective, and practice patterns vary widely. It reviews evidence showing that most melanoma arises de novo, that pathologists have limited agreement and accuracy when classifying melanocytic lesions, and that re-excision often finds no residual nevus and rarely upstages to melanoma. Based on the literature and expert consensus, mildly dysplastic nevi and moderately dysplastic nevi with negative margins can usually be monitored, while severely dysplastic nevi are generally re-excised. For moderately dysplastic nevi with positive margins, a large multicenter study found no same-site melanomas over long follow-up, suggesting observation is reasonable when the lesion was fully removed clinically and follow-up is reliable. The speaker emphasizes that dysplastic nevi are markers of increased melanoma risk rather than true pre-melanomas, encourages complete biopsy when possible, warns that partial biopsies with atypia should prompt complete excision, and stresses incorporating dermoscopic features, pathology nuances, patient anxiety, and clinical context into shared decision-making.

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Conclusions

  • Dysplastic nevi should be viewed as markers of melanoma risk rather than inevitable pre-melanomas.
  • Histologic grading of dysplastic nevi is highly subjective, with only modest agreement and accuracy except at the extremes of benignity and obvious melanoma.
  • Practice patterns vary widely, especially for moderately dysplastic nevi, reflecting uncertainty in their management.
  • Most dysplastic nevi do not recur after biopsy, and upstaging to melanoma on re-excision is rare.
  • Moderately dysplastic nevi with positive margins showed no same-site melanomas in the presented multicenter cohort, supporting observation in selected cases.
  • Close clinical follow-up with routine skin surveillance is reasonable for mild and moderate dysplastic nevi when the lesion has been adequately sampled and no residual pigment remains.
  • Re-excision remains appropriate to consider for severely dysplastic nevi and some moderate-to-severe lesions because of diagnostic uncertainty.
  • Patients with multiple dysplastic nevi have elevated risk for future melanomas elsewhere on the body, so they warrant ongoing surveillance.
  • The decision to re-excise or monitor should incorporate pretest clinical suspicion, dermoscopic features, pathology nuances, patient anxiety, and overall risk context.
  • Shared decision-making and patient education improve understanding and confidence even if they do not necessarily change the ultimate choice of excision versus monitoring.
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