4.3 Article

Shedding light on PRAME expression in dysplastic nevi: a cohort study

Journal

VIRCHOWS ARCHIV
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s00428-023-03720-5

Keywords

PRAME; Dysplastic nevi; Melanoma; Immunohistochemistry; Differential diagnosis; Dermatopathology

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This study explores the expression of PRAME in dysplastic nevi and its potential diagnostic value. The results show heterogeneous expression profiles of PRAME in dysplastic nevi, and PRAME positivity effectively distinguishes high-grade dysplastic nevi from cutaneous melanomas. However, the applicability of PRAME in the differential diagnosis of dysplastic lesions remains unclear as it can yield conflicting results with morphology.
Dysplastic nevi represent one of the least agreed-upon entities in dermatopathology despite the existence of established criteria. This study explores preferentially expressed antigen in melanoma (PRAME) in dysplastic nevi, an uncharted area. We examined 22 common melanocytic nevi (CMN), 20 cutaneous melanomas (CM), 48 low-grade dysplastic nevi (LG-DN), and 40 high-grade dysplastic nevi (HG-DN). PRAME was immunohistochemically assessed using a five-tiered system (0 to 4 +). Among CMN, 59% scored 0, 32% scored 1 + , and 9% scored 2 + . CM had score 2 + and 4 + in 11% and 89% of cases, respectively. Among LG-DN, 38% presented score 0, 31% score 1 + , 17% score 2 + , 8% score 3 + , and 6% score 4 + . Thirty per cent of HG-DN demonstrated a score 0, 30% with score 1 + , 15% score 2 + , 10% score 3 + , and 15% score 4 + . Compared to CMN and CM, LG-DN and HG-DN showed heterogeneous expression profiles of PRAME. PRAME positivity effectively distinguished HG-DN from CM with 85% specificity and 80% sensitivity (p < 0.0001). Predictive values were 87% (negative) and 76% (positive). Furthermore, a trend of increased PRAME expression from LG-DN to HG-DN was observed. However, the applicability of PRAME in the differential diagnosis of dysplastic lesions remains unclear as can yield conflicting results with morphology, which remains the primary diagnostic tool for melanocytic lesions.

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