Abstract
Multicentric pigmented Bowen's disease is a newly recognized entity which affects younger individuals and mainly involves genital areas. It is histologically indistinguishable from Bowen's disease (squamous cell carcinoma in situ) but differs remarkably in its clinical features, prognosis, and management. The case reported here describes such a disease entity and emphasizes the need of correlating clinical information with histopathologic features in arriving at a correct diagnosis.
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