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. 2019 Apr 20;37(4):265-268.
doi: 10.3760/cma.j.issn.1001-9391.2019.04.005.

[Clinical characteristics, treatment and outcome of chronic mercury-related nephrotic syndrome]

[Article in Chinese]
Affiliations

[Clinical characteristics, treatment and outcome of chronic mercury-related nephrotic syndrome]

[Article in Chinese]
Z Z Gao et al. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. .

Abstract

Objective: To investigate the etiology, clinical features, treatment and outcome of nephrotic syndrome associated with chronic mercury poisoning. Methods: From June 2013 to April 2018, Beijing Chaoyang Hospital, Capital Medical University received 33 patients with chronic mercury-neutral nephrotic syndrome. The clinical manifestations, laboratory tests, treatment methods, and outcomes were analyzed. Results: Among the 33 patients, 27 patients had mercury exposure due to daily-life contact and the other 6 patients were caused by iatrogenic mercury. The symptom was characterized by typical nephrotic syndrome such as lower extremity edema and proteinuria at first onset. The treatment was based on mercury-removing treatment, 19 cases were treated with mercury removal alone, 16 cases were completely relieved; 10 cases were treated with mercury removal and glucocorticoids, all of which were completely relieved; 4 cases were treated with mercury removal, glucocorticoids and immunosuppressive agents, all complete remission; clinical complete remission rate is about 90.9% (30 cases in total) . Urinary mercury levels decreased the fastest between the first and second courses of mercury treatment, but the total amount of urine protein increased. As the amount of urinary mercury excreted increased, the total amount of urine protein decreased gradually (Z=2.86, P<0.01) . Conclusion: The clinical features of chronic mercury-induced nephrotic syndrome are non-specific, easy to be misdiagnosed and missed. The treatment is mainly treated with mercury removal treatment. The prognosis is good. In severe cases, glucocorticoid therapy can be supplemented.

目的: 探究慢性汞中毒相关肾病综合征的病因、临床特征、治疗及转归。 方法: 采用横断面方法选择首都医科大学附属北京朝阳医院2013年6月~2018年4月收治的慢性汞中毒性肾病综合征患者33例为研究对象,对其临床表现、实验室检查、治疗方法、转归等进行统计学分析。 结果: 33例患者中生活源性汞接触中毒27例,医源性汞接触6例,首发症状主要表现为下肢水肿、蛋白尿等典型肾病综合征特征。治疗以驱汞治疗为基础,单纯驱汞治疗19例,完全缓解16例;驱汞治疗同时使用糖皮质激素10例,全部完全缓解;驱汞治疗同时使用糖皮质激素及免疫抑制剂治疗4例,全部完全缓解;临床完全缓解率为90.9%(共30例),总体疗效好。第1和2疗程驱汞治疗尿汞水平下降最快,但尿微量总蛋白升高,随着尿汞排出量增加,尿微量总蛋白量逐步下降(Z=2.86,P<0.01)。 结论: 慢性汞中毒性肾病综合征临床特征无特异性,易误诊、漏诊,治疗以驱汞治疗为主要措施,预后良好,严重者可辅以激素治疗。.

Keywords: Clinical features; Mercury poisoning; Nephrotic syndrome; Treatment.

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