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Drug Rash with Eosinophilia and Systemic Symptoms Syndrome Presenting After the Initiation of Staphylococcus hominis Infectious Endocarditis Treatment: A Case Report and Updated Review of Management Considerations

机译:感染人嗜酸性粒细胞和全身症状综合征的药物皮疹开始人型葡萄球菌感染性心内膜炎治疗:病例报告和更新的管理注意事项

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摘要

We present the case of a 62-year-old Caucasian man who was being treated for mitral valve endocarditis via a six-week course of vancomycin. On Day 32 of the treatment, he developed an erythematous, pruritic, desquamating, and painful rash covering 80% of the total body surface area and intermittent fevers. Laboratory findings included leukocytosis with peripheral blood eosinophilia and elevated erythrocyte sedimentation rate, C-reactive protein, and serum creatinine.Although the patient only completed five weeks of antibiotics, the decision was made to not complete the six-week antibiotic course due to suspicion of vancomycin-induced drug rash with eosinophilia and systemic symptoms (DRESS). The patient was then given 80 mg of intramuscular triamcinolone (Kenalog) and advised to apply topical 0.1% triamcinolone twice per day. At the three-month follow-up, the rash, leukocytosis, eosinophilia, and renal dysfunction had resolved. Clinicians must maintain a high index of suspicion for vancomycin-induced DRESS in patients with rash and eosinophilia for early recognition and treatment.DRESS syndrome treatment typically involves discontinuing the causative drug and promptly administering steroids. However, there is a therapeutic dilemma in administering steroids during the course of an active infection. Therefore, this article serves two purposes. First, this case report highlights our approach towards managing a patient with DRESS and concurrent infectious endocarditis. Second, we include a review of the management considerations when prescribing pulsed steroids so that clinicians have a single source as a practical guide towards reducing the potentially severe systemic sequelae in DRESS syndrome and its associated treatment.
机译:我们介绍了一个62岁的白人男子的情况,该人正在通过6周的万古霉素疗程治疗二尖瓣心内膜炎。在治疗的第32天,他出现了红斑,瘙痒,脱皮和疼痛的皮疹,占全身表面积的80%和间歇性发烧。实验室检查结果包括白细胞增多症伴外周血嗜酸性粒细胞增多,红细胞沉降率升高,C反应蛋白和血清肌酐。尽管患者仅完成了5周的抗生素治疗,但由于怀疑存在抗生素而决定不完成6周的抗生素治疗万古霉素引起的皮疹,伴有嗜酸性粒细胞增多和全身症状(DRESS)。然后给患者服用80 mg肌内曲安奈德(Kenalog),建议每天两次局部使用0.1%曲安奈德。在三个月的随访中,皮疹,白细胞增多,嗜酸性粒细胞增多和肾功能不全得到了缓解。对于皮疹和嗜酸性粒细胞增多的患者,临床医生必须高度怀疑万古霉素引起的DRESS,以便及早识别和治疗。DRESS综合征的治疗通常包括停用致病药物并及时给予类固醇药物。然而,在活动性感染过程中给予类固醇存在治疗难题。因此,本文有两个目的。首先,该病例报告突出了我们处理患有DRESS和并发感染性心内膜炎的患者的方法。其次,我们在开具脉冲类固醇时对管理上的考虑进行了回顾,以便临床医生拥有单一来源作为减少DRESS综合征及其相关治疗中潜在的严重系统性后遗症的实用指南。

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