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Bullous Darier’s disease mimicking Hailey-Hailey disease
BACKGROUND: The bullous variant of Darier’s disease (DD) is a rare type characterized by histological and clinical overlap with Hailey-Hailey disease (HDD). CASE REPORTS: The following case report describes two cases of familial DD; a 51-year-old woman who presented with erythematous plaques, covere...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare Communications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437642/ https://www.ncbi.nlm.nih.gov/pubmed/22984662 http://dx.doi.org/10.1007/s13555-011-0007-x |
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author | Khaled, Aida Ben Hamida, Myriam Goucha, Samia Zermani, Rachida Rameh, Soumaya Ben Taazayet, Sabra Kamoun, Mohamed Ridha Fazaa, Bécima |
author_facet | Khaled, Aida Ben Hamida, Myriam Goucha, Samia Zermani, Rachida Rameh, Soumaya Ben Taazayet, Sabra Kamoun, Mohamed Ridha Fazaa, Bécima |
author_sort | Khaled, Aida |
collection | PubMed |
description | BACKGROUND: The bullous variant of Darier’s disease (DD) is a rare type characterized by histological and clinical overlap with Hailey-Hailey disease (HDD). CASE REPORTS: The following case report describes two cases of familial DD; a 51-year-old woman who presented with erythematous plaques, covered by small blisters in axillary and inguinal areas, and the first patient’s daughter, who presented with keratotic papules localized on the axillary and inframammary folds. CONCLUSION: These two cases are original by the predominant flexural distribution, and by a bullous form in the first case, clinically and histologically mimicking HHD. |
format | Online Article Text |
id | pubmed-3437642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Healthcare Communications |
record_format | MEDLINE/PubMed |
spelling | pubmed-34376422012-09-13 Bullous Darier’s disease mimicking Hailey-Hailey disease Khaled, Aida Ben Hamida, Myriam Goucha, Samia Zermani, Rachida Rameh, Soumaya Ben Taazayet, Sabra Kamoun, Mohamed Ridha Fazaa, Bécima Dermatol Ther (Heidelb) Case Report BACKGROUND: The bullous variant of Darier’s disease (DD) is a rare type characterized by histological and clinical overlap with Hailey-Hailey disease (HDD). CASE REPORTS: The following case report describes two cases of familial DD; a 51-year-old woman who presented with erythematous plaques, covered by small blisters in axillary and inguinal areas, and the first patient’s daughter, who presented with keratotic papules localized on the axillary and inframammary folds. CONCLUSION: These two cases are original by the predominant flexural distribution, and by a bullous form in the first case, clinically and histologically mimicking HHD. Springer Healthcare Communications 2011-10-25 /pmc/articles/PMC3437642/ /pubmed/22984662 http://dx.doi.org/10.1007/s13555-011-0007-x Text en © Springer Healthcare 2011 https://creativecommons.org/licenses/by-nc/4.0/ Open Access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Case Report Khaled, Aida Ben Hamida, Myriam Goucha, Samia Zermani, Rachida Rameh, Soumaya Ben Taazayet, Sabra Kamoun, Mohamed Ridha Fazaa, Bécima Bullous Darier’s disease mimicking Hailey-Hailey disease |
title | Bullous Darier’s disease mimicking Hailey-Hailey disease |
title_full | Bullous Darier’s disease mimicking Hailey-Hailey disease |
title_fullStr | Bullous Darier’s disease mimicking Hailey-Hailey disease |
title_full_unstemmed | Bullous Darier’s disease mimicking Hailey-Hailey disease |
title_short | Bullous Darier’s disease mimicking Hailey-Hailey disease |
title_sort | bullous darier’s disease mimicking hailey-hailey disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437642/ https://www.ncbi.nlm.nih.gov/pubmed/22984662 http://dx.doi.org/10.1007/s13555-011-0007-x |
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