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A rare case of chronic Gianotti–Crosti syndrome: A case report

Gianotti–Crosti syndrome, also known as papular acrodermatitis of childhood, is a common, self-limiting dermatosis often seen in children with triggers including viral and bacterial infections along with immunizations. Lesions are generally described as asymptomatic, skin colored to erythematous pap...

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Autores principales: Chin, Laura D, Liy-Wong, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108410/
https://www.ncbi.nlm.nih.gov/pubmed/37077806
http://dx.doi.org/10.1177/2050313X231164250
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author Chin, Laura D
Liy-Wong, Carmen
author_facet Chin, Laura D
Liy-Wong, Carmen
author_sort Chin, Laura D
collection PubMed
description Gianotti–Crosti syndrome, also known as papular acrodermatitis of childhood, is a common, self-limiting dermatosis often seen in children with triggers including viral and bacterial infections along with immunizations. Lesions are generally described as asymptomatic, skin colored to erythematous papules and papulovesicles that often spontaneously resolve within weeks. Here, we will discuss Gianotti–Crosti syndrome and present a rare case of chronic Gianotti–Crosti syndrome in an otherwise healthy 3-year-old male persisting for over 20 months. From this report, we aim to better educate the dermatologic community on the extremes of the Gianotti–Crosti syndrome disease course to improve diagnosis and treatment of symptomatic patients.
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spelling pubmed-101084102023-04-18 A rare case of chronic Gianotti–Crosti syndrome: A case report Chin, Laura D Liy-Wong, Carmen SAGE Open Med Case Rep JCMS Case Report Gianotti–Crosti syndrome, also known as papular acrodermatitis of childhood, is a common, self-limiting dermatosis often seen in children with triggers including viral and bacterial infections along with immunizations. Lesions are generally described as asymptomatic, skin colored to erythematous papules and papulovesicles that often spontaneously resolve within weeks. Here, we will discuss Gianotti–Crosti syndrome and present a rare case of chronic Gianotti–Crosti syndrome in an otherwise healthy 3-year-old male persisting for over 20 months. From this report, we aim to better educate the dermatologic community on the extremes of the Gianotti–Crosti syndrome disease course to improve diagnosis and treatment of symptomatic patients. SAGE Publications 2023-04-14 /pmc/articles/PMC10108410/ /pubmed/37077806 http://dx.doi.org/10.1177/2050313X231164250 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle JCMS Case Report
Chin, Laura D
Liy-Wong, Carmen
A rare case of chronic Gianotti–Crosti syndrome: A case report
title A rare case of chronic Gianotti–Crosti syndrome: A case report
title_full A rare case of chronic Gianotti–Crosti syndrome: A case report
title_fullStr A rare case of chronic Gianotti–Crosti syndrome: A case report
title_full_unstemmed A rare case of chronic Gianotti–Crosti syndrome: A case report
title_short A rare case of chronic Gianotti–Crosti syndrome: A case report
title_sort rare case of chronic gianotti–crosti syndrome: a case report
topic JCMS Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108410/
https://www.ncbi.nlm.nih.gov/pubmed/37077806
http://dx.doi.org/10.1177/2050313X231164250
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