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血液透析患者特发性嗜酸性粒细胞增多综合征:病例报告。

Idiopathic hypereosinophilic syndrome in hemodialysis patients: Case reports.

机构信息

Division of Nephrology, First Department of Integrated Medicine, Saitama Medical Center, Jichi Medical University, Saitama, Japan.

出版信息

Medicine (Baltimore). 2021 Mar 12;100(10):e25164. doi: 10.1097/MD.0000000000025164.

Abstract

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.

摘要

背景

在此,我们报告了 3 例特发性嗜酸性粒细胞增多综合征的血液透析患者,他们使用皮质类固醇治疗获得了成功。

病例介绍

病例 1 为 63 岁男性,因双侧肾切除而行血液透析,出现嗜酸性粒细胞增多伴消化道症状、心肌损伤和透析中低血压。病例 2 为 83 岁男性,因肾动脉硬化而行血液透析,出现嗜酸性粒细胞增多伴瘙痒、心肌损伤和透析中低血压。病例 3 为 59 岁男性,因糖尿病肾病而行血液透析,出现嗜酸性粒细胞增多伴瘙痒、心肌损伤和透析中低血压。

所有 3 例患者均表现为嗜酸性粒细胞增多(嗜酸性粒细胞计数≥1500/μL 超过 1 个月)和多器官受累(透析中低血压、心脏损伤、消化道症状和过敏性皮炎)。系统计算机断层扫描、心电图、超声心动图、骨髓检查和血液检查均未发现嗜酸性粒细胞增多的特定原因。此外,病例 2 和 3 最近没有开始服用任何新药,病例 1 的淋巴细胞刺激试验为阴性。因此,他们被诊断为特发性嗜酸性粒细胞增多综合征。

所有 3 例患者均接受了皮质类固醇治疗,病例 1、2 和 3 分别给予泼尼松 40mg/d、30mg/d 和 60mg/d。

他们的消化道症状、瘙痒、透析中低血压和血清肌钙蛋白 I 浓度立即改善,同时嗜酸性粒细胞计数减少。

结论

血液透析患者中特发性嗜酸性粒细胞增多综合征的病例报告较少。我们认为,记录此类患者的临床发现和治疗情况对于确定特发性嗜酸性粒细胞增多综合征的最佳治疗方法是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74de/7969317/7f48185ed1e1/medi-100-e25164-g001.jpg

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