Carbamazepine Induced Stevens-Johnson Syndrome That Developed into Toxic Epidermal Necrolysis: Review of the Literature.

Q3 Medicine
Yousef S Abuzneid, Hussam I A Alzeerelhouseini, Duha Rabi, Ihab Hilail, Hatem Rjoob, Abdelrahman Rabee, Naser Amro, Qutaiba Qafisheh, Mohammad Kharraz
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引用次数: 3

Abstract

Background: Stevens-Johnson syndrome and toxic epidermal necrolysis are both skin diseases believed to be following the pattern of a type IV hypersensitivity mechanism, which can be triggered by infectious agents or administration of a variety of drugs as part of the spectrum of severe cutaneous adverse reactions (SCARs). Fever and blisters, that peel forming painful raw areas, are early symptoms of this condition, and complications such as dehydration, sepsis, pneumonia, and multiple organ failure are typically seen during the course of the disease. Case Presentation. We present a case of a 23-year-old female patient referred to our hospital after taking carbamazepine and developing high-grade fever and ulcers that appeared initially in her mouth and face but then progressed despite treatment, extending all over her body and involving about 90% of her BSA.

Conclusion: The use of IVIG and plasmapheresis was a good management for our case, helping in our patient's well-being and recovery. Even if there is no stipulated guideline treatment for cases of SJS and TEN, we think that further investigations about IVIG and plasmapheresis should be investigated as a possible way to treat both conditions.

Abstract Image

卡马西平诱导的史蒂文斯-约翰逊综合征发展为中毒性表皮坏死松解:文献综述。
背景:史蒂文斯-约翰逊综合征和中毒性表皮坏死松解症都是被认为遵循IV型超敏反应机制模式的皮肤病,可由感染性病原体或多种药物引起,作为严重皮肤不良反应(scar)的一部分。发热和水疱(剥落形成疼痛的原始区域)是这种疾病的早期症状,脱水、败血症、肺炎和多器官衰竭等并发症通常在疾病过程中出现。案例演示。我们报告一例23岁的女性患者,在服用卡马西平后,出现高热和溃疡,最初出现在口腔和面部,但尽管治疗,病情仍在发展,并扩展到全身,累及约90%的BSA。结论:IVIG +血浆置换是一种很好的治疗方法,有助于患者的健康和康复。即使SJS和TEN病例没有规定的指导治疗方法,我们认为应该进一步研究IVIG和血浆置换作为治疗这两种疾病的可能方法。
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
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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