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Allopurinol-Induced Stevens–Johnson Syndrome (SJS)

Allopurinol is a commonly used medication that lowers uric acid production which is essential for gout treatment and prevention. Although many patients tolerate allopurinol therapy without severe complications; Stevens–Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are life-threatening...

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Autores principales: Anis, Takla R, Meher, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557962/
https://www.ncbi.nlm.nih.gov/pubmed/37811521
http://dx.doi.org/10.2147/CPAA.S427714
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author Anis, Takla R
Meher, John
author_facet Anis, Takla R
Meher, John
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description Allopurinol is a commonly used medication that lowers uric acid production which is essential for gout treatment and prevention. Although many patients tolerate allopurinol therapy without severe complications; Stevens–Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are life-threatening delayed hypersensitivity reactions that have been reported especially among Asian and African American patients. We describe a case of allopurinol-induced SJS in a 95-year-old Asian female. The patient started allopurinol 13 days prior to presenting to the emergency room (ER). On day 10 of therapy, the patient developed a diffuse erythematous desquamating rash which prompted her to visit the ER after 3 days from the rash onset. This case report describes a rare fatal hypersensitivity reaction that requires rapid identification and treatment in a multi-disciplinary setting.
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spelling pubmed-105579622023-10-07 Allopurinol-Induced Stevens–Johnson Syndrome (SJS) Anis, Takla R Meher, John Clin Pharmacol Case Report Allopurinol is a commonly used medication that lowers uric acid production which is essential for gout treatment and prevention. Although many patients tolerate allopurinol therapy without severe complications; Stevens–Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are life-threatening delayed hypersensitivity reactions that have been reported especially among Asian and African American patients. We describe a case of allopurinol-induced SJS in a 95-year-old Asian female. The patient started allopurinol 13 days prior to presenting to the emergency room (ER). On day 10 of therapy, the patient developed a diffuse erythematous desquamating rash which prompted her to visit the ER after 3 days from the rash onset. This case report describes a rare fatal hypersensitivity reaction that requires rapid identification and treatment in a multi-disciplinary setting. Dove 2023-10-02 /pmc/articles/PMC10557962/ /pubmed/37811521 http://dx.doi.org/10.2147/CPAA.S427714 Text en © 2023 Anis and Meher. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Report
Anis, Takla R
Meher, John
Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title_full Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title_fullStr Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title_full_unstemmed Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title_short Allopurinol-Induced Stevens–Johnson Syndrome (SJS)
title_sort allopurinol-induced stevens–johnson syndrome (sjs)
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557962/
https://www.ncbi.nlm.nih.gov/pubmed/37811521
http://dx.doi.org/10.2147/CPAA.S427714
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