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Gianotti-Crosti syndrome: a case report of a teenager

Gianotti-Crosti syndrome is a rare disease characterized by acral papular eruption with symmetrical distribution. It is a benign and self-limited disease; the symptoms disappear after two to eight weeks, without recurrences or scars. Skin lesions are usually asymptomatic. Prodrome might occur, sugge...

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Autores principales: Pedreira, Renata Leite, Leal, Juliana Martins, Silvestre, Keline Jácome, Lisboa, Alice Paixão, Gripp, Alexandre Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325029/
https://www.ncbi.nlm.nih.gov/pubmed/28300930
http://dx.doi.org/10.1590/abd1806-4841.20164410
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author Pedreira, Renata Leite
Leal, Juliana Martins
Silvestre, Keline Jácome
Lisboa, Alice Paixão
Gripp, Alexandre Carlos
author_facet Pedreira, Renata Leite
Leal, Juliana Martins
Silvestre, Keline Jácome
Lisboa, Alice Paixão
Gripp, Alexandre Carlos
author_sort Pedreira, Renata Leite
collection PubMed
description Gianotti-Crosti syndrome is a rare disease characterized by acral papular eruption with symmetrical distribution. It is a benign and self-limited disease; the symptoms disappear after two to eight weeks, without recurrences or scars. Skin lesions are usually asymptomatic. Prodrome might occur, suggesting upper respiratory infection, or constitutional symptoms. Diagnosis is eminently clinical, and this disease is associated with viral infections. Due to its rarity and low occurrence in adolescents and adults, we report a case of Gianotti-Crosti syndrome of a teenager.
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spelling pubmed-53250292017-03-02 Gianotti-Crosti syndrome: a case report of a teenager Pedreira, Renata Leite Leal, Juliana Martins Silvestre, Keline Jácome Lisboa, Alice Paixão Gripp, Alexandre Carlos An Bras Dermatol Case Report Gianotti-Crosti syndrome is a rare disease characterized by acral papular eruption with symmetrical distribution. It is a benign and self-limited disease; the symptoms disappear after two to eight weeks, without recurrences or scars. Skin lesions are usually asymptomatic. Prodrome might occur, suggesting upper respiratory infection, or constitutional symptoms. Diagnosis is eminently clinical, and this disease is associated with viral infections. Due to its rarity and low occurrence in adolescents and adults, we report a case of Gianotti-Crosti syndrome of a teenager. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5325029/ /pubmed/28300930 http://dx.doi.org/10.1590/abd1806-4841.20164410 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pedreira, Renata Leite
Leal, Juliana Martins
Silvestre, Keline Jácome
Lisboa, Alice Paixão
Gripp, Alexandre Carlos
Gianotti-Crosti syndrome: a case report of a teenager
title Gianotti-Crosti syndrome: a case report of a teenager
title_full Gianotti-Crosti syndrome: a case report of a teenager
title_fullStr Gianotti-Crosti syndrome: a case report of a teenager
title_full_unstemmed Gianotti-Crosti syndrome: a case report of a teenager
title_short Gianotti-Crosti syndrome: a case report of a teenager
title_sort gianotti-crosti syndrome: a case report of a teenager
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325029/
https://www.ncbi.nlm.nih.gov/pubmed/28300930
http://dx.doi.org/10.1590/abd1806-4841.20164410
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