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Updated: Sep 30, 2025

Comparative Lesions Analysis Through a Targeted Sequencing Approach
Published on: November 5, 2019
Comparative Analysis of PRAME Expression in 127 Acral and Nail Melanocytic Lesions
Giacomo Santandrea1,2, Riccardo Valli1, Eleonora Zanetti1
1Pathology Unit.
Abstract:
PRAME (PReferentially expressed Antigen in MElanoma), a cancer testis antigen expressed in low levels in gonadal, endometrial, and adrenal gland tissues, has been recently considered a valuable tool in the differential diagnosis between benign and malignant melanocytic lesions. The aim of the current study is to perform PRAME immunostaining on a large series of benign and malignant acral lesions to evaluate the reproducibility of data reported in the literature and to validate PRAME as an affordable tool in the differential diagnosis between benign and malignant acral melanocytic tumors. Immunohistochemical analysis for PRAME was performed in 127 benign and malignant acral and nail melanocytic lesions. To better correlate PRAME expression with the nature (benign vs. malignant) of the lesions, we categorized PRAME tumor cells percentage positivity and intensity in a cumulative score obtained by adding the quartile of positive tumor cells (0, 1+, 2+, 3+, 4+) to PRAME expression intensity in tumor cells (0, 1+, 2+, 3+). Adopting an arbitrary PRAME expression score of < 5 versus ≥5 resulted in a correct identification of 82.5% of benign and 87.1% of malignant lesions. PRAME immunohistochemistry demonstrated good sensitivity and specificity in the diagnosis of acral melanocytic lesions, however, in line with the previous literature, we identified a subset of challenging cases such as acral Spitz nevi, in situ melanomas, and small, thin, invasive melanomas in which PRAME did not correlate with morphologic features. This suggests that PRAME can be a valid tool to be incorporated in a diagnostic clinicopathologic algorithm, subject to morphologic characteristics.
Insights
PRAME immunostaining shows promise for differentiating benign and malignant acral melanocytic tumors, achieving high accuracy. However, challenging cases like Spitz nevi and early melanomas require careful morphologic correlation.
Area of Science:
- Oncology
- Dermatopathology
- Immunohistochemistry
Background:
- PRAME (PReferentially expressed Antigen in MElanoma) is a cancer testis antigen.
- It shows potential in distinguishing benign from malignant melanocytic lesions.
- Acral melanocytic tumors present diagnostic challenges.
Purpose of the Study:
- To evaluate PRAME immunostaining in a large series of acral melanocytic lesions.
- To assess PRAME's reproducibility and diagnostic utility in differentiating benign and malignant tumors.
- To validate PRAME as an affordable diagnostic tool for acral lesions.
Main Methods:
- Immunohistochemical analysis of PRAME was performed on 127 benign and malignant acral and nail melanocytic lesions.
- A cumulative scoring system for PRAME expression (percentage and intensity) was developed.
- Lesions were categorized based on a PRAME expression score threshold.
Main Results:
- An arbitrary PRAME score threshold correctly identified 82.5% of benign and 87.1% of malignant lesions.
- PRAME immunohistochemistry demonstrated good sensitivity and specificity for acral melanocytic lesions.
- Challenging cases (Spitz nevi, in situ/thin invasive melanomas) showed discordant PRAME expression.
Conclusions:
- PRAME immunostaining is a valuable tool for diagnosing acral melanocytic lesions.
- It can be incorporated into diagnostic algorithms alongside morphologic assessment.
- Careful consideration of challenging cases where PRAME expression may not correlate with morphology is necessary.
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