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Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report

Stevens–Johnson syndrome (SJS) is an acute life-threatening mucocutaneous reaction caused by excessive necrosis and detachment of the epidermis. It is commonly drug induced and phenytoin is a common precipitant. Phenytoin, an antiepileptic drug, is also known to cause myocarditis. Phenytoin causing...

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Autor principal: Kodliwadmath, Ashwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513850/
https://www.ncbi.nlm.nih.gov/pubmed/28744164
http://dx.doi.org/10.2147/IMCRJ.S135643
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author Kodliwadmath, Ashwin
author_facet Kodliwadmath, Ashwin
author_sort Kodliwadmath, Ashwin
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description Stevens–Johnson syndrome (SJS) is an acute life-threatening mucocutaneous reaction caused by excessive necrosis and detachment of the epidermis. It is commonly drug induced and phenytoin is a common precipitant. Phenytoin, an antiepileptic drug, is also known to cause myocarditis. Phenytoin causing both myocarditis and SJS in the same patient is very rare and can lead to increased morbidity and mortality. Here, we describe the case of a 43-year-old male who developed SJS and myocarditis secondary to phenytoin. In spite of aggressive resuscitative efforts, the patient could not be revived. Thus, a combination of myocarditis with SJS increases the mortality and should be considered in patients with SJS secondary to phenytoin and associated shock.
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spelling pubmed-55138502017-07-25 Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report Kodliwadmath, Ashwin Int Med Case Rep J Case Report Stevens–Johnson syndrome (SJS) is an acute life-threatening mucocutaneous reaction caused by excessive necrosis and detachment of the epidermis. It is commonly drug induced and phenytoin is a common precipitant. Phenytoin, an antiepileptic drug, is also known to cause myocarditis. Phenytoin causing both myocarditis and SJS in the same patient is very rare and can lead to increased morbidity and mortality. Here, we describe the case of a 43-year-old male who developed SJS and myocarditis secondary to phenytoin. In spite of aggressive resuscitative efforts, the patient could not be revived. Thus, a combination of myocarditis with SJS increases the mortality and should be considered in patients with SJS secondary to phenytoin and associated shock. Dove Medical Press 2017-07-10 /pmc/articles/PMC5513850/ /pubmed/28744164 http://dx.doi.org/10.2147/IMCRJ.S135643 Text en © 2017 Kodliwadmath. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Kodliwadmath, Ashwin
Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title_full Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title_fullStr Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title_full_unstemmed Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title_short Phenytoin-induced Stevens–Johnson syndrome with myocarditis: a rare case report
title_sort phenytoin-induced stevens–johnson syndrome with myocarditis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513850/
https://www.ncbi.nlm.nih.gov/pubmed/28744164
http://dx.doi.org/10.2147/IMCRJ.S135643
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