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Idiopathic hypereosinophilic syndrome in hemodialysis patients

机译:血液透析患者的特发性过嗜酸性综合征

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RATIONALE:Herein, we report 3 hemodialysis patients with idiopathic hypereosinophilic syndrome who were successfully treated using corticosteroid therapy.PATIENT CONCERNS:Case 1 was a 63-year-old man who was undergoing hemodialysis because of bilateral nephrectomy and developed hypereosinophilia with digestive symptoms, myocardial injury, and intradialytic hypotension. Case 2 was an 83-year-old man who was undergoing hemodialysis because of nephrosclerosis and developed hypereosinophilia with pruritus, myocardial injury, and intradialytic hypotension. Case 3 was a 59-year-old man who was undergoing hemodialysis because of diabetic nephropathy and developed hypereosinophilia with pruritus, myocardial injury, and intradialytic hypotension.DIAGNOSES:All 3 patients presented with hypereosinophilia (eosinophil count ≥1500?/μL for more than 1?month) and multiple-organ involvement (intradialytic hypotension, cardiac injury, digestive symptoms, and allergic dermatitis). A specific cause for the hypereosinophilia was not identified by systemic computed tomography, electrocardiography, echocardiography, bone marrow examination, or blood tests. Furthermore, Case 2 and 3 had not recently started taking any new drugs and drug-induced lymphocyte stimulation tests were negative in Case 1. Therefore, they were diagnosed with idiopathic hypereosinophilic syndrome.INTERVENTIONS:All 3 patients received corticosteroid therapy with prednisolone at a dose of 40?mg/d, 30?mg/d, and 60?mg/d in Case 1, 2, and 3, respectively.OUTCOMES:Their digestive symptoms, pruritus, intradialytic hypotension, and serum troponin I concentrations were immediately improved alongside reductions in their eosinophil counts.LESSONS:There have been few case reports of idiopathic hypereosinophilic syndrome in patients undergoing hemodialysis. We believe that recording of the clinical findings and treatments of such patients is mandatory to establish the optimal management of idiopathic hypereosinophilic syndrome.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:理由:在此,我们报告3血液透析患者具有成功治疗的特发性低渗综合征,这些患者使用皮质类固醇治疗成功治疗。案例1是一名63岁的男子,由于双侧肾切除术和产生了消化症状的低渗菌,心肌卵细胞损伤和细胞内低血压。案例2是由于肾脏粥样硬化和瘙痒,心肌损伤和细胞发育性低血压的血液渗症和发育性低血压,是一名83岁的男子正在进行血液透析。案例3是一个59岁的男子,由于糖尿病肾病和瘙痒,心肌损伤和细胞发育性低血压和发育性低血压的过度粒细胞症。诊断:所有3名患者患有过稳态粒细胞症(嗜酸性粒细胞计数≥1500?/μl超过1?月份)和多器官参与(脑内低血压,心脏损伤,消化症状和过敏性皮炎)。通过全身计算断层扫描,心电图,超声心动图,骨髓检查或血液试验未鉴定过稳态粒细胞症的特异性原因。此外,案例2和3最近未开始服用任何新药,并且药物诱导的淋巴细胞刺激测试是阴性的。因此,它们被诊断出具有特发性过稳态综合征的患者。interventions:所有3名患者在剂量下接受皮质类固醇治疗的皮质类固醇治疗在1,2和3的情况下,40×mg / d,30?mg / d和60?mg / d和60?mg / d。其消化症状,瘙痒,细胞内低血压和血清肌钙蛋白,我浓度立即伴随着减少他们的嗜酸性粒细胞统计学:在进行血液透析患者中​​有很少有特发性过稳态综合征的病症报告。我们认为,录制这些患者的临床发现和治疗是强制性的,以建立特发性低渗综合征的最佳管理.Copyright? 2021提交人。由Wolters Kluwer Health,Inc。出版

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