Porokeratosis is an uncommon disorder of keratinization that presents with keratotic papules or annular plaques with an elevated border. The distinct histologic hallmark of porokeratosis is cornoid lamella, a column of tightly fitted parakeratotic cells in the upper epidermis. There are multiple clinical variants of porokeratosis, including:
Disseminated superficial actinic porokeratosis
Classical porokeratosis of Mibelli
Porokeratosis plantaris, palmaris, et disseminate
Linear porokeratosis
Additionally, rare variants include:
Genitogluteal porokeratosis
Facial porokeratosis
Giant porokeratosis
Porokeratosis ptychotropica
Hypertrophic verrucous porokeratosis
Eruptive pruritic papular porokeratosis
Follicular porokeratosis
Reticulate porokeratosis
Variants can occur together but rarely do. Porokeratosis is a precancerous lesion that can undergo malignant transformation. Evaluation of porokeratosis is best conducted with a biopsy of the elevated border. Although multiple therapies exist for porokeratosis (including topical, systemic, and surgical), there are no standard guidelines for treatment.
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