A Case of Vancomycin-Induced Drug Reaction with Eosinophilia, Systemic Symptoms and Multiorgan Involvement Proven Using Lymphocyte Transformation Test.

IF 1.5 4区 医学 Q3 DERMATOLOGY Annals of Dermatology Pub Date : 2023-04-01 DOI:10.5021/ad.20.341
Kyung Bae Chung, Ji-Hye Hwang, Doyoung Kim
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Abstract

Drug-induced hypersensitivity syndrome (DiHS), also referred to as drug reaction with eosinophilia and systemic symptoms (DRESS), is a rare but potentially life-threatening condition induced by drug hypersensitivity that leads to significant morbidity and mortality and often occurs in patients undergoing combination antibiotic therapy. Due to a recent increase in the incidence of methicillin-resistant Staphylococcus aureus infections, the occurrence of vancomycin-induced DiHS/DRESS has increased rapidly. However, because of insufficient pharmacogenetic data on vancomycin-induced drug eruptions in Asians coupled with the risk of re-eliciting the symptoms by provocation tests, confirmation of the culprit drug in vancomycin-induced DiHS/DRESS is often challenging. Here, we report a case of vancomycin-induced DiHS/DRESS, where the causal relationship was confirmed using a lymphocyte transformation test (LTT). A 51-year-old woman was treated with combination antibiotics, including vancomycin, for infective pericarditis. The patient subsequently developed fever, facial edema, generalized rash followed by multiple internal organ involvement, including the kidney, lung, liver, and heart. Thus, based on the International Registry of Severe Cutaneous Adverse Reaction (RegiSCAR) criteria, the case was diagnosed as 'definite' DiHS/DRESS, although the culprit drug was obscured by combination antibiotic therapy. The LTT confirmed that vancomycin, but not other glycopeptide antibiotics, specifically induced T-cell proliferation in this case. Collectively, our case suggests that clinicians can utilize LTT to identify the causative medication of DiHS/DRESS when the clinical information is limited to defining the culprit drug.

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淋巴细胞转化试验证实万古霉素致药物反应伴嗜酸性粒细胞增多、全身症状及多器官受累1例
药物性超敏反应综合征(DiHS),也称为嗜酸性粒细胞增多和全身症状的药物反应(DRESS),是一种罕见但可能危及生命的疾病,由药物超敏反应引起,可导致显著的发病率和死亡率,常发生在接受联合抗生素治疗的患者中。由于最近耐甲氧西林金黄色葡萄球菌感染发生率的增加,万古霉素诱导的DiHS/DRESS的发生率迅速增加。然而,由于万古霉素在亚洲引起的药疹的药理学数据不足,再加上诱发试验有再次引起症状的风险,因此确定万古霉素引起的DiHS/DRESS的罪魁祸首药物往往具有挑战性。在这里,我们报告了一例万古霉素诱导的DiHS/DRESS,其中因果关系通过淋巴细胞转化试验(LTT)得到证实。一例51岁妇女因感染性心包炎接受包括万古霉素在内的联合抗生素治疗。患者随后出现发热、面部水肿、全身皮疹,并累及多个内脏器官,包括肾、肺、肝和心脏。因此,根据国际严重皮肤不良反应登记处(RegiSCAR)的标准,该病例被诊断为“明确的”DiHS/DRESS,尽管联合抗生素治疗掩盖了罪魁祸首药物。LTT证实万古霉素特异性诱导t细胞增殖,而不是其他糖肽抗生素。总的来说,我们的病例表明,当临床信息仅限于确定罪魁祸首药物时,临床医生可以利用LTT来识别DiHS/DRESS的病因药物。
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来源期刊
Annals of Dermatology
Annals of Dermatology 医学-皮肤病学
CiteScore
1.60
自引率
6.20%
发文量
77
审稿时长
6-12 weeks
期刊介绍: Annals of Dermatology (Ann Dermatol) is the official peer-reviewed publication of the Korean Dermatological Association and the Korean Society for Investigative Dermatology. Since 1989, Ann Dermatol has contributed as a platform for communicating the latest research outcome and recent trend of dermatology in Korea and all over the world. Ann Dermatol seeks for ameliorated understanding of skin and skin-related disease for clinicians and researchers. Ann Dermatol deals with diverse skin-related topics from laboratory investigations to clinical outcomes and invites review articles, original articles, case reports, brief reports and items of correspondence. Ann Dermatol is interested in contributions from all countries in which good and advanced research is carried out. Ann Dermatol willingly recruits well-organized and significant manuscripts with proper scope throughout the world.
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