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Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association
Pachyonychia Congenita (PC) refers to a group of autosomal dominant disorders with variable clinical presentations. While nail dystrophy and plantar keratoderma are the most consistent features in all the variants, a myriad of other manifestations has been observed. This report highlights a case of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724318/ https://www.ncbi.nlm.nih.gov/pubmed/29263544 http://dx.doi.org/10.4103/ijd.IJD_473_16 |
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author | Ghosh, Romana Chatterjee, Kingshuk Barua, Jayanta Kumar Roy, Anupam |
author_facet | Ghosh, Romana Chatterjee, Kingshuk Barua, Jayanta Kumar Roy, Anupam |
author_sort | Ghosh, Romana |
collection | PubMed |
description | Pachyonychia Congenita (PC) refers to a group of autosomal dominant disorders with variable clinical presentations. While nail dystrophy and plantar keratoderma are the most consistent features in all the variants, a myriad of other manifestations has been observed. This report highlights a case of young female presenting with multiple asymptomatic cutaneous cysts associated with plantar kearatoderma and nail dystrophy. Similar nail changes were evident in her son also. Such clinical presentation, in corroboration with histopathological evaluation of the cutaneous cyst prompted us to make a diagnosis of Pachyonychia Congenita type II. |
format | Online Article Text |
id | pubmed-5724318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57243182017-12-20 Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association Ghosh, Romana Chatterjee, Kingshuk Barua, Jayanta Kumar Roy, Anupam Indian J Dermatol Case Report Pachyonychia Congenita (PC) refers to a group of autosomal dominant disorders with variable clinical presentations. While nail dystrophy and plantar keratoderma are the most consistent features in all the variants, a myriad of other manifestations has been observed. This report highlights a case of young female presenting with multiple asymptomatic cutaneous cysts associated with plantar kearatoderma and nail dystrophy. Similar nail changes were evident in her son also. Such clinical presentation, in corroboration with histopathological evaluation of the cutaneous cyst prompted us to make a diagnosis of Pachyonychia Congenita type II. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5724318/ /pubmed/29263544 http://dx.doi.org/10.4103/ijd.IJD_473_16 Text en Copyright: © 2017 Indian Journal of Dermatology 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Ghosh, Romana Chatterjee, Kingshuk Barua, Jayanta Kumar Roy, Anupam Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title | Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title_full | Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title_fullStr | Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title_full_unstemmed | Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title_short | Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association |
title_sort | cutaneous cysts with nail dystrophy in a young female: a classical association |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724318/ https://www.ncbi.nlm.nih.gov/pubmed/29263544 http://dx.doi.org/10.4103/ijd.IJD_473_16 |
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