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Disseminated Superficial Actinic Porokeratosis in a Mother and Daughter: A Case Report
Gayatri M Gunale1, Sudhir Singh1, Sabha Neazee1
1Dermatology, Datta Meghe Medical College, Datta Meghe Institute of Higher Education and Research (Deemed to be University), Nagpur, IND.
Abstract:
Porokeratosis is an autosomal dominant condition of epidermal keratinization. There are many clinical and morphological variants of porokeratosis, the most prevalent of which is disseminated superficial actinic porokeratosis (DSAP), which commonly affects photoexposed areas. Here, we present a 52-year-old woman and her 24-year-old daughter having similar complaints of gradually enlarging, annular hyperpigmented plaques on photoexposed areas suggesting familial transmission. Diagnosed as DSAP, treatment with oral isotretinoin and topical keratolytics showed significant improvement within one and a half months. This case report highlights familial DSAP cases in a mother and daughter, which is rare, emphasizing the importance of early diagnosis and management for better outcomes and reduced malignancy risk.
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