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Acute Generalised Exanthematous Pustulosis: An Update

Acute generalised exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction and is attributed to drugs in more than 90% of cases. It is a rare disease, with an estimated incidence of 1–5 patients per million per year. The clinical manifestations characterised by the rapid development of...

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Autores principales: De, Abhishek, Das, Sudip, Sarda, Aarti, Pal, Dayamay, Biswas, Projna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838751/
https://www.ncbi.nlm.nih.gov/pubmed/29527022
http://dx.doi.org/10.4103/ijd.IJD_581_17
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author De, Abhishek
Das, Sudip
Sarda, Aarti
Pal, Dayamay
Biswas, Projna
author_facet De, Abhishek
Das, Sudip
Sarda, Aarti
Pal, Dayamay
Biswas, Projna
author_sort De, Abhishek
collection PubMed
description Acute generalised exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction and is attributed to drugs in more than 90% of cases. It is a rare disease, with an estimated incidence of 1–5 patients per million per year. The clinical manifestations characterised by the rapid development of sterile pustular lesions, fever and leucocytosis. Number of drugs has been reported to be associated with AGEP, most common being the antibiotics. Histopathologically there is intraepidermal pustules and papillary dermal oedema with neutrophilic and eosinophilic infiltrations. Systemic involvement can be present in more severe cases. Early diagnosis with withdrawal of the causative drug is the most important step in the management. Treatment includes supportive care, prevention of antibiotics and use of a potent topical steroid.
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spelling pubmed-58387512018-03-09 Acute Generalised Exanthematous Pustulosis: An Update De, Abhishek Das, Sudip Sarda, Aarti Pal, Dayamay Biswas, Projna Indian J Dermatol IJD® Symposium Acute generalised exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction and is attributed to drugs in more than 90% of cases. It is a rare disease, with an estimated incidence of 1–5 patients per million per year. The clinical manifestations characterised by the rapid development of sterile pustular lesions, fever and leucocytosis. Number of drugs has been reported to be associated with AGEP, most common being the antibiotics. Histopathologically there is intraepidermal pustules and papillary dermal oedema with neutrophilic and eosinophilic infiltrations. Systemic involvement can be present in more severe cases. Early diagnosis with withdrawal of the causative drug is the most important step in the management. Treatment includes supportive care, prevention of antibiotics and use of a potent topical steroid. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5838751/ /pubmed/29527022 http://dx.doi.org/10.4103/ijd.IJD_581_17 Text en Copyright: © 2018 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 IJD® Symposium
De, Abhishek
Das, Sudip
Sarda, Aarti
Pal, Dayamay
Biswas, Projna
Acute Generalised Exanthematous Pustulosis: An Update
title Acute Generalised Exanthematous Pustulosis: An Update
title_full Acute Generalised Exanthematous Pustulosis: An Update
title_fullStr Acute Generalised Exanthematous Pustulosis: An Update
title_full_unstemmed Acute Generalised Exanthematous Pustulosis: An Update
title_short Acute Generalised Exanthematous Pustulosis: An Update
title_sort acute generalised exanthematous pustulosis: an update
topic IJD® Symposium
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838751/
https://www.ncbi.nlm.nih.gov/pubmed/29527022
http://dx.doi.org/10.4103/ijd.IJD_581_17
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