Expression of Melan-A in cutaneous granular cell tumours: a diagnostic pitfall

Pathology. 2024 Feb;56(1):47-51. doi: 10.1016/j.pathol.2023.09.009. Epub 2023 Nov 1.

Abstract

Morphological overlap exists between cutaneous granular cell tumours (GCT) and malignant melanoma, with the melanocyte-specific markers HMB45 and Melan-A commonly used to support the diagnosis of melanoma. We recently encountered several cases of GCT in our practice showing strong expression of Melan-A. The aim of this study was to establish the prevalence of positive immunohistochemical staining for Melan-A and HMB45 in a series of unequivocal GCTs. We also aimed to assess the prevalence of staining for PRAME (PReferentially expressed Antigen in MElanoma), a marker expressed in >80% of primary melanomas as well as many non-melanocytic tumours. A total of 20 cutaneous/subcutaneous GCTs were evaluated using Melan-A, HMB45 and PRAME immunohistochemistry. Staining for Melan-A and HMB45 was scored using a semiquantitative scale from 0 (absent) to 3+ (staining present in >50% of tumour cells). PRAME expression was recorded as either positive (>75% of cell nuclei staining) or negative. Melan-A expression was observed in four GCTs (20%), with strong and diffuse (3+) staining seen in two cases (10%), both from anogenital areas. Weak patchy nuclear PRAME expression was seen in every case, interpreted to be negative. HMB45 was also negative in all cases (100%). Our study demonstrates that Melan-A expression can be strong and diffuse in a subset of otherwise unequivocal cutaneous GCTs, which may cause diagnostic confusion with malignant melanoma. HMB45 and PRAME did not stain any of the GCTs in our series.

Keywords: Granular cell tumour; HMB45; Melan-A; PRAME; diagnosis; immunohistochemistry; melanoma; pathology.

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, Neoplasm / metabolism
  • Biomarkers, Tumor / metabolism
  • Diagnosis, Differential
  • Granular Cell Tumor* / diagnosis
  • Humans
  • MART-1 Antigen
  • Melanoma* / pathology
  • Skin Neoplasms* / pathology
  • Transcription Factors

Substances

  • MART-1 Antigen
  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • Antibodies, Monoclonal
  • Transcription Factors
  • PRAME protein, human