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Warfarin‐induced Stevens–Johnson syndrome with severe liver injury
Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a life-threatening mucocutaneous disease that is predominantly drug-induced. Warfarin is the most commonly used drug for long-term anti-coagulant therapy; however, warfarin-induced SJS/TEN is seldom reported. In this study, we presente...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320577/ https://www.ncbi.nlm.nih.gov/pubmed/34311601 http://dx.doi.org/10.1177/03000605211033196 |
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author | Xiong, Hao Liu, Tao Xiao, Jieping Wan, Jianji Yang, Jie Huang, Gengshi Han, Yongzhi Liu, Guangren Dong, Xiuqin |
author_facet | Xiong, Hao Liu, Tao Xiao, Jieping Wan, Jianji Yang, Jie Huang, Gengshi Han, Yongzhi Liu, Guangren Dong, Xiuqin |
author_sort | Xiong, Hao |
collection | PubMed |
description | Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a life-threatening mucocutaneous disease that is predominantly drug-induced. Warfarin is the most commonly used drug for long-term anti-coagulant therapy; however, warfarin-induced SJS/TEN is seldom reported. In this study, we presented the case of a 61-year-old man who developed SJS after receiving multiple-drug therapy following aortic valve replacement surgery. The patient was diagnosed with drug-induced liver injury (DILI) based on significantly abnormal liver function test results. Warfarin was identified as the culprit drug using the algorithm of drug causality for epidermal necrolysis (ALDEN) score, enzyme-linked immunospot (ELISPOT) assay, and Roussel Uclaf Causality Assessment Method (RUCAM). After warfarin discontinuation and corticosteroid therapy, the lesions and liver function test findings improved. Human leukocyte antigen typing was conducted to detect the risk allele. To our knowledge, this is the first reported case of warfarin-induced SJS/TEN with DILI. This case suggests that commonly used and safe pharmaceutical agents such as warfarin can potentially cause serious adverse events, including SJS/TEN and DILI. The application of ALDEN, the ELISPOT assay, and RUCAM could be useful in identifying culprit drugs. |
format | Online Article Text |
id | pubmed-8320577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-83205772021-08-09 Warfarin‐induced Stevens–Johnson syndrome with severe liver injury Xiong, Hao Liu, Tao Xiao, Jieping Wan, Jianji Yang, Jie Huang, Gengshi Han, Yongzhi Liu, Guangren Dong, Xiuqin J Int Med Res Case Reports Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a life-threatening mucocutaneous disease that is predominantly drug-induced. Warfarin is the most commonly used drug for long-term anti-coagulant therapy; however, warfarin-induced SJS/TEN is seldom reported. In this study, we presented the case of a 61-year-old man who developed SJS after receiving multiple-drug therapy following aortic valve replacement surgery. The patient was diagnosed with drug-induced liver injury (DILI) based on significantly abnormal liver function test results. Warfarin was identified as the culprit drug using the algorithm of drug causality for epidermal necrolysis (ALDEN) score, enzyme-linked immunospot (ELISPOT) assay, and Roussel Uclaf Causality Assessment Method (RUCAM). After warfarin discontinuation and corticosteroid therapy, the lesions and liver function test findings improved. Human leukocyte antigen typing was conducted to detect the risk allele. To our knowledge, this is the first reported case of warfarin-induced SJS/TEN with DILI. This case suggests that commonly used and safe pharmaceutical agents such as warfarin can potentially cause serious adverse events, including SJS/TEN and DILI. The application of ALDEN, the ELISPOT assay, and RUCAM could be useful in identifying culprit drugs. SAGE Publications 2021-07-26 /pmc/articles/PMC8320577/ /pubmed/34311601 http://dx.doi.org/10.1177/03000605211033196 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Xiong, Hao Liu, Tao Xiao, Jieping Wan, Jianji Yang, Jie Huang, Gengshi Han, Yongzhi Liu, Guangren Dong, Xiuqin Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title | Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title_full | Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title_fullStr | Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title_full_unstemmed | Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title_short | Warfarin‐induced Stevens–Johnson syndrome with severe liver injury |
title_sort | warfarin‐induced stevens–johnson syndrome with severe liver injury |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320577/ https://www.ncbi.nlm.nih.gov/pubmed/34311601 http://dx.doi.org/10.1177/03000605211033196 |
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