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. 1994 May;30(5 Pt 1):707-14.
doi: 10.1016/s0190-9622(08)81499-5.

A multiobserver, population-based analysis of histologic dysplasia in melanocytic nevi

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Free article

A multiobserver, population-based analysis of histologic dysplasia in melanocytic nevi

M W Piepkorn et al. J Am Acad Dermatol. 1994 May.
Free article

Abstract

Background: Nevi that are clinically atypical and histologically dysplastic have been associated with increased melanoma risk. There are few reproducibility studies or population-based studies of nevus histology.

Objective: Our purpose was to quantify concordance in histologic diagnosis of melanocytic lesions among a diverse group of pathologists, to assess intraobserver concordance by comparing readings of the same slide as well as of adjacent recuts from the same block, to correlate histology with nevus appearance and melanoma risk, and to estimate the range of prevalence of histologic dysplasia.

Methods: Histologic slides were prepared from 149 tissue blocks of pigmented lesions from melanoma cases, relatives, and controls. Six dermatopathologists independently evaluated the lesions for histologic dysplasia, without prior agreement on criteria.

Results: According to kappa statistics, intraobserver reproducibility was substantial, and interobserver concordance was fair, despite differences in criteria. The estimated prevalences of histologic dysplasia for the six pathologists ranged from 7% to 32%. Histologic dysplasia was correlated with nevus size for most observers, confounding the observed correlation between nevus appearance and histology.

Conclusion: Although experienced dermatopathologists use different diagnostic criteria for histologic dysplasia, their usage is consistent. Histologic changes ascribed to melanocytic dysplasia are prevalent in the white population for all pathologists. The term nevus with histologic dysplasia should be used in preference to dysplastic nevus.

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Comment in

  • Dysplastic nevi revisited.
    Weinstock MA. Weinstock MA. J Am Acad Dermatol. 1994 May;30(5 Pt 1):807-10. doi: 10.1016/s0190-9622(08)81524-1. J Am Acad Dermatol. 1994. PMID: 8176030 No abstract available.

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