Suppr超能文献

药物超敏反应伴嗜酸性粒细胞增多和全身症状病理生理学的新见解

New Insights into Drug Reaction with Eosinophilia and Systemic Symptoms Pathophysiology.

作者信息

Musette Philippe, Janela Baptiste

机构信息

Dermatology Department, Rouen University Hospital, Rouen, France.

Singapore Immunology Network, Singapore, Singapore.

出版信息

Front Med (Lausanne). 2017 Dec 4;4:179. doi: 10.3389/fmed.2017.00179. eCollection 2017.

Abstract

Drug reaction with eosinophilia and systemic symptoms (DRESS), also known as drug-induced hypersensitivity syndrome, is a severe type of cutaneous drug-induced eruption. DRESS may be a difficult disease to diagnose since the symptoms mimic those of cutaneous and systemic infectious pathologies and can appear up to 3 months after the initial culprit drug exposure. The symptoms of DRESS syndrome include rash development after a minimum of 3 weeks after the onset of a new medication, associated with facial edema, lymphadenopathy, and fever. Biological findings include liver abnormalities, leukocytosis, eosinophilia, atypical lymphocytosis, and reactivation of certain human herpes viruses. In DRESS, liver, kidneys, and lungs are frequently involved in disease evolution. Patients with serious systemic involvement are treated with oral corticosteroids, and full recovery is achieved in the majority of cases. DRESS is a rare disease, and little is known about factors that predict its occurrence. The key features of this reaction are eosinophil involvement, the role of the culprit drug, and virus reactivation that trigger an inappropriate systemic immune response in DRESS patients. Interestingly, it was evidenced that at-risk individuals within a genetically restricted population shared a particular HLA loci. In this respect, a limited number of well-known drugs were able to induce DRESS. This review describes the up-to-date advances in our understanding of the pathogenesis of DRESS.

摘要

药物超敏反应伴嗜酸性粒细胞增多和全身症状(DRESS),也称为药物性超敏反应综合征,是一种严重的皮肤药物性皮疹。DRESS可能是一种难以诊断的疾病,因为其症状与皮肤和全身感染性疾病的症状相似,且可能在首次接触致病药物后长达3个月出现。DRESS综合征的症状包括在开始使用新药物至少3周后出现皮疹,并伴有面部水肿、淋巴结病和发热。生物学检查结果包括肝脏异常、白细胞增多、嗜酸性粒细胞增多、非典型淋巴细胞增多以及某些人类疱疹病毒的再激活。在DRESS中,肝脏、肾脏和肺部在疾病进展过程中经常受累。有严重全身受累的患者用口服糖皮质激素治疗,大多数病例可完全康复。DRESS是一种罕见疾病,对于预测其发生的因素知之甚少。这种反应的关键特征是嗜酸性粒细胞参与、致病药物的作用以及病毒再激活,这些因素会在DRESS患者中引发不适当的全身免疫反应。有趣的是,有证据表明,在一个基因受限的人群中,有风险的个体共享一个特定的HLA基因座。在这方面,少数知名药物能够诱发DRESS。本综述描述了我们对DRESS发病机制理解的最新进展。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验