Vancomycin-Induced Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome Masquerading as Elusive Sepsis.

Pub Date : 2019-04-10 eCollection Date: 2019-01-01 DOI:10.1155/2019/1625010
Sumon Roy, Vinay P Goswamy, Kirolos N Barssoum, Devesh Rai
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引用次数: 4

Abstract

We present a unique case of vancomycin-induced drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome masquerading as elusive endocarditis. A 37-year-old female actively using intravenous drugs presented with worsening right upper extremity pain, fever, and chills. Workup revealed methicillin-resistant staphylococcus aureus (MRSA) bacteremia and multiple right-sided septic pulmonary emboli. Echocardiogram was negative for vegetation. Vancomycin was initiated for bacteremia management suspected secondary to right upper extremity abscesses. However, despite resolution of abscesses, fevers persisted, raising suspicion for endocarditis not detected by echocardiogram. On hospital day 25, the patient began showing signs of DRESS syndrome, ultimately manifesting as transaminitis, eosinophilia, and a diffuse, maculopapular rash. Vancomycin was switched to Linezolid and she improved on high dose steroids. The persistent fevers throughout this hospital course were thought to be an elusive endocarditis before DRESS syndrome fully manifested. Although Vancomycin-induced DRESS is uncommon, this case highlights the importance of identifying early signs of significant adverse effects.

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万古霉素诱导的药物反应与嗜酸性粒细胞增多和全身症状(DRESS)综合征伪装成难以捉摸的败血症。
我们提出一个独特的万古霉素引起的药物反应与嗜酸性粒细胞增多和全身症状(DRESS)综合征伪装为难以捉摸的心内膜炎。一名37岁女性,积极使用静脉注射药物,表现为右上肢疼痛加重,发烧和发冷。检查发现耐甲氧西林金黄色葡萄球菌(MRSA)菌血症和多发右侧脓毒性肺栓塞。超声心动图显示植被阴性。开始使用万古霉素治疗怀疑继发于右上肢脓肿的菌血症。然而,尽管脓肿消退,发烧持续存在,超声心动图未检测到心内膜炎的怀疑。住院第25天,患者开始出现DRESS综合征的症状,最终表现为转氨炎、嗜酸性粒细胞增多和弥漫性黄斑丘疹。万古霉素改为利奈唑胺,大剂量类固醇治疗改善。在DRESS综合征完全表现出来之前,整个住院过程中的持续发热被认为是一种难以捉摸的心内膜炎。虽然万古霉素引起的DRESS并不常见,但该病例强调了识别明显不良反应早期迹象的重要性。
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