Vauthey Laetitia, Uçkay Ilker, Abrassart Sophie, Bernard Louis, Assal Mathieu, Ferry Tristan, Djordjevic Marina, Roussos Constantinos, Vaudaux Pierre
Orthopaedic Surgery Service, University Hospitals of Geneva, Geneva, Switzerland.
Pharmacology. 2008;82(2):138-41. doi: 10.1159/000142729. Epub 2008 Jul 8.
DRESS syndrome (drug rash with eosinophilia and systemic symptoms) is a hypersensitivity reaction with skin rashes, eosinophilia, fever, lymph node enlargement and internal organ involvement.
A 60-year-old diabetic woman was hospitalized at the University Hospitals of Geneva for mid-leg amputation due to peripheral arterial occlusive disease. No drug allergy was reported. Because of a wound infection by methicillin-resistant Staphylococcus aureus, treatment with vancomycin (2 g/day) in continuous perfusion was initiated. Approximately 2 weeks later, she developed a toxidermia with fever, a progressive maculopapular skin rash, eosinophilia and acute renal insufficiency. The skin biopsy revealed a necrosis with lymphocytic and eosinophilic infiltrations, supporting the suspicion of DRESS syndrome. A cure was achieved by the withdrawal of vancomycin and the administration of methylprednisolone (1 g/day), antihistaminics and topical mometasone, without the introduction of other antibiotics.
Vancomycin can be a cause of DRESS syndrome. A high index of suspicion is warranted in order not to miss this potentially lethal disease.
中毒性表皮坏死松解症伴嗜酸性粒细胞增多和全身症状(DRESS综合征)是一种伴有皮疹、嗜酸性粒细胞增多、发热、淋巴结肿大及内脏受累的超敏反应。
一名60岁的糖尿病女性因外周动脉闭塞性疾病在日内瓦大学医院住院接受小腿中段截肢手术。未报告有药物过敏史。因耐甲氧西林金黄色葡萄球菌伤口感染,开始持续静脉滴注万古霉素(2克/天)治疗。大约2周后,她出现了伴有发热的中毒性皮病、进行性斑丘疹皮疹、嗜酸性粒细胞增多及急性肾功能不全。皮肤活检显示有坏死伴淋巴细胞和嗜酸性粒细胞浸润,支持中毒性表皮坏死松解症伴嗜酸性粒细胞增多和全身症状(DRESS综合征)的怀疑。停用万古霉素并给予甲泼尼龙(1克/天)、抗组胺药和外用莫米松后病情得以治愈,未使用其他抗生素。
万古霉素可能是中毒性表皮坏死松解症伴嗜酸性粒细胞增多和全身症状(DRESS综合征)的病因。为避免漏诊这种潜在致命性疾病,需要高度怀疑。