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首页> 外文期刊>Case Reports & Clinical Practice Review >Vancomycin-Induced Leukocytoclastic Vasculitis and Acute Renal Failure Due to Tubulointerstitial Nephritis
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Vancomycin-Induced Leukocytoclastic Vasculitis and Acute Renal Failure Due to Tubulointerstitial Nephritis

机译:万古霉素诱导的白细胞碎裂性血管炎和肾小管间质性肾炎引起的急性肾功能衰竭

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Objective: Unusual or unexpected effect of treatmentBackground: Methicillin-resistant Staphylococcus aureus (MRSA) bacteremia and sepsis are commonly treated with intrave- nous vancomycin. However, vancomycin treatment is associated adverse reactions, including skin rashes and nephrotoxicity. We present a case of acute renal failure due to acute tubulointerstitial nephritis associated with a diffuse leukocytoclastic vasculitic skin eruption following intravenous vancomycin treatment. Case Report: A 79-year-old Caucasian male patient was treated with intravenous vancomycin for MRSA bacteremia. Prior to treatment, his creatinine was normal at 0.6 mg/dl. He presented one week later with shortness of breath, low - er limb edema, and acute renal failure. He had a diffuse maculopapular rash involving the trunk and both up- per and lower extremities. A renal biopsy and left arm skin biopsy were examined histologically. The skin bi- opsy showed leukocytoclastic vasculitis. Renal biopsy showed some sclerosed glomeruli, some with mesangial proliferation, and tubulointerstitial inflammation with eosinophils and plasma cells and mild interstitial fibro- sis. Although there was some renal arteriolosclerosis, no vasculitic changes were seen, and no vascular throm- bosis was present. A diagnosis of leukocytoclastic vasculitis and acute tubulointerstitial nephritis secondary to intravenous vancomycin therapy was made. Conclusions: Although skin reactions associated with drug therapy are common, vancomycin-associated dermal vasculitis is rare. Tubulointerstitial nephritis is also a rare association with vancomycin treatment. This case report has highlighted that patients being treated with intravenous vancomycin should be carefully observed for acute skin rashes and deterioration in renal function, which can be managed by ceasing treatment with vancomycin, steroid challenge, and preventing future exposure to similar antimicrobial agents.
机译:目的:治疗效果异常或出乎意料背景:耐甲氧西林金黄色葡萄球菌(MRSA)菌血症和败血症通常用万古霉素静脉内治疗。但是,万古霉素治疗会引起不良反应,包括皮疹和肾毒性。我们介绍了由于万古霉素治疗后伴有弥漫性白细胞碎裂性血管性皮肤喷发而引起的急性肾小管间质性肾炎引起的急性肾衰竭的病例。病例报告:一名79岁的白人男性患者接受静脉万古霉素治疗MRSA菌血症。在治疗之前,他的肌酐为0.6 mg / dl正常。一周后,他出现呼吸急促,下肢水肿和急性肾衰竭。他患有弥漫性黄斑丘疹,皮疹累及躯干以及上下肢。组织学检查肾活检和左臂皮肤活检。皮肤双眼显示为白细胞碎裂性血管炎。肾活检显示肾小球硬化,肾小球膜增生,嗜酸性粒细胞和浆细胞的肾小管间质发炎,轻度间质纤维化。尽管有一些肾小动脉硬化,但未见血管变化,也未见血管血栓形成。诊断为继发万古霉素治疗后的白细胞碎裂性血管炎和急性肾小管间质性肾炎。结论:尽管与药物治疗相关的皮肤反应很常见,但万古霉素相关的皮肤血管炎很少见。肾小管间质性肾炎也是万古霉素治疗的罕见关联。该病例报告强调,应仔细观察接受静脉内万古霉素治疗的患者的急性皮疹和肾功能恶化,可通过停止使用万古霉素治疗,类固醇刺激并防止将来再接触类似的抗菌剂来治疗。

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