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Acrokeratosis verruciformis of Hopf in family

Acrokeratosis verruciformis of Hopf (AKV) is a rare disorder of keratinization inherited in an autosomal dominant fashion. A 15-year-old female presented with numerous skin-colored papular lesions over the neck as well as dorsa of the hands and feet of 7 years duration. Similar lesions were noted in...

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Autores principales: Agrawal, Sanjay N., Jane, Subodhkumar D., Rawal, Anuprita A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252943/
https://www.ncbi.nlm.nih.gov/pubmed/25506556
http://dx.doi.org/10.4103/2229-5178.144509
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author Agrawal, Sanjay N.
Jane, Subodhkumar D.
Rawal, Anuprita A.
author_facet Agrawal, Sanjay N.
Jane, Subodhkumar D.
Rawal, Anuprita A.
author_sort Agrawal, Sanjay N.
collection PubMed
description Acrokeratosis verruciformis of Hopf (AKV) is a rare disorder of keratinization inherited in an autosomal dominant fashion. A 15-year-old female presented with numerous skin-colored papular lesions over the neck as well as dorsa of the hands and feet of 7 years duration. Similar lesions were noted in her mother. Six other members of her family showed similar lesions with similar site of involvement. Presence of characteristic warty papules and histopathology led to diagnosis of a rare condition of acrokeratosis verruciformis.
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spelling pubmed-42529432014-12-12 Acrokeratosis verruciformis of Hopf in family Agrawal, Sanjay N. Jane, Subodhkumar D. Rawal, Anuprita A. Indian Dermatol Online J Case Report Acrokeratosis verruciformis of Hopf (AKV) is a rare disorder of keratinization inherited in an autosomal dominant fashion. A 15-year-old female presented with numerous skin-colored papular lesions over the neck as well as dorsa of the hands and feet of 7 years duration. Similar lesions were noted in her mother. Six other members of her family showed similar lesions with similar site of involvement. Presence of characteristic warty papules and histopathology led to diagnosis of a rare condition of acrokeratosis verruciformis. Medknow Publications & Media Pvt Ltd 2014-11 /pmc/articles/PMC4252943/ /pubmed/25506556 http://dx.doi.org/10.4103/2229-5178.144509 Text en Copyright: © Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Agrawal, Sanjay N.
Jane, Subodhkumar D.
Rawal, Anuprita A.
Acrokeratosis verruciformis of Hopf in family
title Acrokeratosis verruciformis of Hopf in family
title_full Acrokeratosis verruciformis of Hopf in family
title_fullStr Acrokeratosis verruciformis of Hopf in family
title_full_unstemmed Acrokeratosis verruciformis of Hopf in family
title_short Acrokeratosis verruciformis of Hopf in family
title_sort acrokeratosis verruciformis of hopf in family
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252943/
https://www.ncbi.nlm.nih.gov/pubmed/25506556
http://dx.doi.org/10.4103/2229-5178.144509
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