Allopurinol-Induced Stevens-Johnson Syndrome (SJS).

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Clinical Pharmacology : Advances and Applications Pub Date : 2023-10-02 eCollection Date: 2023-01-01 DOI:10.2147/CPAA.S427714
Takla R Anis, John Meher
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引用次数: 0

Abstract

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.

别嘌呤醇诱导的Stevens-Johnson综合征(SJS)。
别嘌呤醇是一种常用的降低尿酸生成的药物,尿酸生成对痛风的治疗和预防至关重要。尽管许多患者耐受别嘌呤醇治疗而没有严重并发症;Stevens-Johnson综合征(SJS)和中毒性表皮坏死松解症(TEN)是危及生命的迟发性超敏反应,尤其在亚裔和非裔美国人中有报道。我们描述了一例95岁亚洲女性别嘌呤醇诱导的SJS。患者在进入急诊室(ER)前13天开始服用别嘌呤醇。在治疗的第10天,患者出现弥漫性红斑性脱屑皮疹,这促使她在皮疹发作3天后去急诊室就诊。本病例报告描述了一种罕见的致命超敏反应,需要在多学科环境中快速识别和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
14
审稿时长
16 weeks
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