Abstract

Melanocytic nevi, including dysplastic or atypical nevi (DN), can recur or persist following shave removal procedures, and recurrence may resemble melanoma, both clinically and histologically (pseudomelanoma). Recurrence may originate from proliferation of the remaining neoplastic melanocytes following incomplete removal. The present study determines the rate and etiology of this event. A cross-sectional analysis of 110 excision specimens showing histological recurrence was performed, and these specimens were compared to the slides of the original shave specimens showing mildly atypical DN. In the second portion of the study, a retrospective review of 167 cases with biopsy-proven mildly atypical DN which were followed up for at least two years was conducted to determine the rate of recurrence/persistence. When followed up for two years, DN, with positive shave margins, defined by extension or very close extension (≤0.2 mm) of the lesions to the lateral margins and into the deep margins through the hair follicles in the shave removal specimens, have a higher probability of recurrence than DN with negative (or clear) margins (odds ratio (OR) = 158; 95% confidence interval (CI) = 36.62–683; P < 0.001). The overall rate of histologically confirmed recurrence/persistence was approximately 10%.

Highlights

  • Dysplastic or atypical nevi (DN) are one of the most frequently encountered lesions in dermatopathology

  • Architectural atypia includes lentiginous proliferation at the dermoepidermal junction extending beyond the dermal component, elongation and bridging of adjacent epidermal rete ridges, and lamellar fibrosis in the papillary dermis, which is often accompanied by perivascular lymphocytic infiltrate

  • No shave specimen showed dermal atypical melanocytes extending to the deep margins

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Summary

Introduction

Dysplastic or atypical nevi (DN) are one of the most frequently encountered lesions in dermatopathology. The prevalence of histological DN varies by race and ethnicity and can reach up to 50% in some white populations [1]. DN are typically graded into three categories of mild, moderate, and severely atypical DN, which involve architectural atypia and cytological atypia. Architectural atypia includes lentiginous proliferation at the dermoepidermal junction extending beyond the dermal component (shoulder phenomena), elongation and bridging of adjacent epidermal rete ridges, and lamellar fibrosis in the papillary dermis, which is often accompanied by perivascular lymphocytic infiltrate. Cytological atypia is based on nuclear enlargement, hyperchromasia, uneven distribution of chromatin, presence of conspicuous cytoplasm with dusty pigmentation, and prominence of the nucleoli [5, 6]

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