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[Multifocal vulvar pigmentation: Don't ignore a rare diagnosis]
Sara Laurent-Roussel1, Françoise Plantier1
1Service de pathologie, hôpital Cochin-Tarnier, 27 rue du Faubourg Saint-Jacques, 75014 Paris, France.
Annales De Pathologie
|December 6, 2021
Summary
Vulvar melanoma, a rare cancer, often lacks pigment and appears in multiple sites. Its histological type is lentiginous, frequently associated with distant melanocytic hyperplasia.
Area of Science:
- Oncology
- Dermatology
- Pathology
Background:
- Vulvar melanoma is a rare malignancy with incompletely understood origins.
- It exhibits distinct characteristics compared to cutaneous melanoma, including frequent achromia and multifocality.
- The lentiginous histological subtype (MLM) is predominant.
Purpose of the Study:
- To elucidate the unique pathological features of vulvar melanoma.
- To compare and contrast vulvar melanoma with its cutaneous counterpart.
- To investigate the association with distant lentiginous melanocytic hyperplasia.
Main Methods:
- Histopathological analysis of vulvar melanoma cases.
- Comparative study with cutaneous melanoma data.
- Evaluation of adjacent and distant melanocytic lesions.
Main Results:
- Vulvar melanoma frequently presents as achromic (non-pigmented) lesions.
- Multifocality is a common characteristic of vulvar melanoma.
- Lentiginous melanocytic hyperplasia at a distance was observed in approximately 50% of cases.
Conclusions:
- Vulvar melanoma possesses unique clinical and pathological features.
- The lentiginous histological type (MLM) is characteristic.
- The high incidence of associated distant lentiginous melanocytic hyperplasia warrants further investigation.
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