Case report details diagnosis and treatment of eruptive pruritic papular porokeratosis, indicating its rarity.
Eruptive pruritic papular porokeratosis (EPPP) is a rare inflammatory variant of disseminated superficial porokeratosis characterized by the sudden onset of pruritic papules, primarily affecting the extremities and trunk. We present the case of a 77-year-old male who developed EPPP without any underlying malignancy or immunosuppression. Histopathology confirmed EPPP, and the patient underwent treatment with topical lovastatin 2% ointment, followed by topical calcipotriene. This report highlights the clinical presentation, diagnostic workup, therapeutic interventions, and emerging insights into the management of this uncommon condition.
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Dookie et al. (2025) studied this question.
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