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CASE REPORT
Year : 2017  |  Volume : 10  |  Issue : 2  |  Page : 195-197

Macular variant of acrokeratosis verruciformis of Hopf


Department of Skin and VD, Shree Krishna Hospital, Karamsad, Gujarat, India

Correspondence Address:
Rita Vipul Vora
OPD No. 111, Shree Krishna Hospital, Anand, Karamsad - 388 325, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0975-2870.202096

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Acrokeratosis verruciformis (AKV) of Hopf is an autosomal dominant condition characterized by multiple flesh-colored or lightly pigmented flat or convex warty papules over dorsa of hands, feet, knees, elbows, and forearms. It affects both sexes and is usually present at birth or appears in early childhood. Two forms of the disease have been described, namely, classical AKV and sporadic AKV. Histological examination differentiates it from other similar conditions. Superficial ablation is the treatment of choice. We represent a case of a young female with extensive lesions over contralateral limbs, of classical AKV interspersed with multiple hypopigmented macular lesions of AKV.


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