Rifaximin induced Stevens-Johnson syndrome in a patient of acute on chronic liver failure

C. Philips, C. Kalal, Amrish Sahney, K. Kumar
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Abstract

Stevens-Johnson Syndrome (SJS) forms part of a spectrum of severe adverse cutaneous reactions that can eventually culminate into toxic epidermal necrolysis (TEN), a potentially fatal condition. Drugs, most commonly allopurinol, antivirals, antiepileptics, sulfonamides and other antibiotics are implicated in this disease, even though, many case reports and series describe a variety of associations with many other classes of drugs. Infectious and inflammatory conditions also predispose to this severe cutaneous disease. Here, we present a patient who was initially diagnosed as a case of acute on chronic liver failure in hepatic encephalopathy grade I, in whom the introduction of rifaximin therapy led to aggressive cutaneous reactions, leading to SJS, which was managed with intensive supportive treatment because of which the patient improved substantially and was discharged after 14 days of onset of a potentially fatal condition. Rifaximin therapy leading to SJS-TEN has been reported only once before.
利福昔明致急性或慢性肝衰竭患者斯蒂文斯-约翰逊综合征
史蒂文斯-约翰逊综合征(SJS)是一系列严重皮肤不良反应的一部分,最终可导致中毒性表皮坏死松解(TEN),这是一种潜在的致命疾病。药物,最常见的是别嘌呤醇,抗病毒药物,抗癫痫药,磺胺类药物和其他抗生素与这种疾病有关,尽管许多病例报告和系列描述了与许多其他类别药物的各种关联。感染和炎症状况也易导致这种严重的皮肤病。在这里,我们报告了一位最初被诊断为肝性脑病I级急性慢性肝衰竭的患者,该患者引入利福昔明治疗导致侵袭性皮肤反应,导致SJS,并通过强化支持治疗进行管理,因此患者明显改善,并在发病14天后出院,这可能是致命的疾病。利福昔明治疗导致SJS-TEN之前仅报道过一次。
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