Publication: Mixed Variant of Acrokeratosis verruciformis of Hopf: A rare entity
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Date
2021
Journal Title
Journal ISSN
Volume Title
Publisher
Society of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
Abstract
Abstract:
Acrokeratosis verruciformis of Hopf (AKV) is a rare autosomal dominant genodermatosis of unknown etiology. Here we present a case of a 20-year-female with multiple skin-colored flat papules over the dorsum of hands and feet interspersed with multiple hypopigmented macular lesions of 5 years duration. No family member showed a similar lesion. The presence of classical AKV with absent family history and definite histopathology findings make this case an unusual and rare entity.
Description
Sonia P Jain
Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra, India
https://orcid.org/0000-0002-3376-2250
Pratiksha Sonkusale
Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra, India
Abhay Vilas Deshmukh
Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra, India
Pallavi Kumari
Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra, India
Keywords
Acrokeratosis verruciformis of Hopf, Genodermatosis, Hypopigmented macules