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Related Experiment Videos

VS38 immunostaining in melanocytic lesions

J H Shanks1, S S Banerjee

  • 1Department of Histopathology, Christie Hospital NHS Trust, Withington, Manchester.

Journal of Clinical Pathology
|March 1, 1996
PubMed
Summary

The monoclonal antibody VS38, a marker for plasma cells, is frequently positive in malignant melanoma, including rare mucosal melanomas. This finding is crucial for diagnosing undifferentiated tumors, especially at unusual sites like the nasal cavity.

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Area of Science:

  • Oncology
  • Immunohistochemistry
  • Dermatopathology

Background:

  • The monoclonal antibody VS38 is a known marker for reactive/neoplastic plasma cells, aiding in diagnosing plasmacytoma, myeloma, and lymphomas.
  • A recent observation of a plasmacytoid melanoma showing strong VS38 immunoreactivity highlighted a potential diagnostic pitfall.

Purpose of the Study:

  • To investigate the immunoreactivity of VS38 in a spectrum of melanocytic lesions, both benign and malignant.
  • To assess the utility and potential diagnostic errors of VS38 in identifying tumor lineage, particularly in challenging cases.

Main Methods:

  • The study utilized the Streptavidin-peroxidase complex technique on 167 paraffin-embedded melanocytic lesions.
  • Chromogen selection (DAB or nickel/DAB) was adapted based on the pigmentation level of the lesions.

Main Results:

  • VS38 immunostaining was positive in 92% of primary cutaneous melanomas, 100% of primary mucosal melanomas, and 91.7% of recurrent/metastatic melanomas.
  • Positive staining was also observed in 14.5% of benign nevi (including Spitz nevi) and 10.5% of dysplastic nevi/in situ melanomas.
  • Clear cell sarcomas of soft tissues also showed 100% positivity.

Conclusions:

  • VS38 immunostaining is frequently positive in malignant melanoma, both primary and metastatic, and less commonly in benign nevi.
  • The results emphasize the importance of considering malignant melanoma in undifferentiated tumors with VS38 reactivity, especially those arising in unusual locations.
  • Clinicians should be aware of this potential diagnostic overlap when using VS38 for tumor lineage identification.

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