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...

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Main Authors: Hao Xiong, Tao Liu, Jieping Xiao, Jianji Wan, Jie Yang, Gengshi Huang, Yongzhi Han, Guangren Liu, Xiuqin Dong
Format: Article
Language:English
Published: SAGE Publishing 2021-07-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605211033196
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spelling doaj-e1b819ada7c74134a57f325585a9a8df2021-07-27T22:03:29ZengSAGE PublishingJournal of International Medical Research1473-23002021-07-014910.1177/03000605211033196Warfarin‐induced Stevens–Johnson syndrome with severe liver injuryHao XiongTao LiuJieping XiaoJianji WanJie YangGengshi HuangYongzhi HanGuangren LiuXiuqin DongStevens–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.https://doi.org/10.1177/03000605211033196
collection DOAJ
language English
format Article
sources DOAJ
author Hao Xiong
Tao Liu
Jieping Xiao
Jianji Wan
Jie Yang
Gengshi Huang
Yongzhi Han
Guangren Liu
Xiuqin Dong
spellingShingle Hao Xiong
Tao Liu
Jieping Xiao
Jianji Wan
Jie Yang
Gengshi Huang
Yongzhi Han
Guangren Liu
Xiuqin Dong
Warfarin‐induced Stevens–Johnson syndrome with severe liver injury
Journal of International Medical Research
author_facet Hao Xiong
Tao Liu
Jieping Xiao
Jianji Wan
Jie Yang
Gengshi Huang
Yongzhi Han
Guangren Liu
Xiuqin Dong
author_sort Hao Xiong
title Warfarin‐induced Stevens–Johnson syndrome with severe liver injury
title_short 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_sort warfarin‐induced stevens–johnson syndrome with severe liver injury
publisher SAGE Publishing
series Journal of International Medical Research
issn 1473-2300
publishDate 2021-07-01
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.
url https://doi.org/10.1177/03000605211033196
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