Aberrant expression of HMB-45 in traumatized melanocytic nevi

Todd M Leleux1, Victor G Prieto, A Hafeez Diwan

  • 1Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA.

Abstract

Insights

Traumatized melanocytic nevi (TMN) can exhibit altered HMB-45 staining, mimicking melanoma. Evaluating MIB-1 expression and trauma-specific histology aids accurate diagnosis of these benign nevi.

Area of Science:

  • Dermatopathology
  • Oncology
  • Immunohistochemistry

Background:

  • Histologic and immunohistochemical assessment using HMB-45 and anti-Ki-67 aids in differentiating benign melanocytic nevi (BMN) from malignant melanoma.
  • Previous research indicated loss of maturation and aberrant immunohistochemical findings in melanocytic nevi post-cryotherapy.
  • This study investigates a similar phenomenon in traumatized melanocytic nevi (TMN).

Purpose of the Study:

  • To evaluate the histologic and immunohistochemical characteristics of traumatized nevi at early and late stages.
  • To identify potential diagnostic challenges in distinguishing traumatized nevi from melanoma.

Main Methods:

  • Retrieved 24 cases of traumatized melanocytic nevi (TMN) from pathology archives.
  • Assessed cases using HMB-45 and MIB-1 (for Ki-67) antibodies.
  • Evaluated by two independent pathologists.

Main Results:

  • TMN exhibited epidermal changes (parakeratosis, ulceration, crusting) and dermal changes (fibrosis, melanophages).
  • Architectural disorder of melanocytes was observed, with basal layer crowding but no significant pagetoid spread.
  • Fifty-four percent of TMN lacked typical HMB-45 maturation, showing strong labeling in nevus cells within or beneath the scar; no significant Ki-67 labeling was noted.

Conclusions:

  • Loss of HMB-45 maturation in TMN can be a diagnostic pitfall, potentially mimicking melanoma.
  • Concurrent evaluation of MIB-1 expression and characteristic histologic features of trauma is crucial for accurate diagnosis.
  • The precise time interval between trauma and biopsy could not be determined.

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