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Eosinophilic annular erythema in adults: report of two cases and review of the literature

We herein report two cases of eosinophilic annular erythema in adults, which is rare. In both patients, lesions developed rapidly in few days and were located mainly on the trunk, buttocks, and extremities. Diagnosis was histopathological, with typical features including acute dermal inflammatory in...

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Autores principales: Heras, Marta Olivé, Muñoz, Noelia Pérez, Sancho, Maribel Iglesias, Millet, Pablo Umbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726681/
https://www.ncbi.nlm.nih.gov/pubmed/29267450
http://dx.doi.org/10.1590/abd1806-4841.20176373
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author Heras, Marta Olivé
Muñoz, Noelia Pérez
Sancho, Maribel Iglesias
Millet, Pablo Umbert
author_facet Heras, Marta Olivé
Muñoz, Noelia Pérez
Sancho, Maribel Iglesias
Millet, Pablo Umbert
author_sort Heras, Marta Olivé
collection PubMed
description We herein report two cases of eosinophilic annular erythema in adults, which is rare. In both patients, lesions developed rapidly in few days and were located mainly on the trunk, buttocks, and extremities. Diagnosis was histopathological, with typical features including acute dermal inflammatory infiltrate with abundant eosinophils. One of the patients recurred after treatment on three occasions and finally cured spontaneously. The second patient recurred once and was then successfully treated with topical clobetasol. Clinical and histopathological features of eosinophilic annular erythema in adults have rarely been reported. A review of the literature and discussion of relationship with Wells syndrome are also included.
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spelling pubmed-57266812017-12-18 Eosinophilic annular erythema in adults: report of two cases and review of the literature Heras, Marta Olivé Muñoz, Noelia Pérez Sancho, Maribel Iglesias Millet, Pablo Umbert An Bras Dermatol Case Report We herein report two cases of eosinophilic annular erythema in adults, which is rare. In both patients, lesions developed rapidly in few days and were located mainly on the trunk, buttocks, and extremities. Diagnosis was histopathological, with typical features including acute dermal inflammatory infiltrate with abundant eosinophils. One of the patients recurred after treatment on three occasions and finally cured spontaneously. The second patient recurred once and was then successfully treated with topical clobetasol. Clinical and histopathological features of eosinophilic annular erythema in adults have rarely been reported. A review of the literature and discussion of relationship with Wells syndrome are also included. Sociedade Brasileira de Dermatologia 2017 /pmc/articles/PMC5726681/ /pubmed/29267450 http://dx.doi.org/10.1590/abd1806-4841.20176373 Text en ©2017 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Case Report
Heras, Marta Olivé
Muñoz, Noelia Pérez
Sancho, Maribel Iglesias
Millet, Pablo Umbert
Eosinophilic annular erythema in adults: report of two cases and review of the literature
title Eosinophilic annular erythema in adults: report of two cases and review of the literature
title_full Eosinophilic annular erythema in adults: report of two cases and review of the literature
title_fullStr Eosinophilic annular erythema in adults: report of two cases and review of the literature
title_full_unstemmed Eosinophilic annular erythema in adults: report of two cases and review of the literature
title_short Eosinophilic annular erythema in adults: report of two cases and review of the literature
title_sort eosinophilic annular erythema in adults: report of two cases and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726681/
https://www.ncbi.nlm.nih.gov/pubmed/29267450
http://dx.doi.org/10.1590/abd1806-4841.20176373
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