引起急性肾损伤和肾病综合征的“神奇药丸”。

Clinical nephrology. Case studies Pub Date : 2025-09-04 eCollection Date: 2025-01-01 DOI:10.5414/CNCS111804
Yangming Cao, Thao Phan, Patil Armenian, Jonathan E Zuckerman
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引用次数: 0

摘要

摘要:突发性肾病综合征(NS)和急性间质性肾炎(AIN)似乎是一种罕见但独特的非甾体抗炎药(NSAID)相关的肾脏综合征。病例介绍:我们提出这样一个病例的病人谁采取了“神奇药丸”痛风。肾活检显示微小病变(MCD)、急性间质性肾炎(AIN)、严重急性肾小管损伤(ATI)和IgA肾病(IgAN)。他接受了一个流产疗程的大剂量强的松治疗,肾脏疾病完全解决。MCD和AIN联合的病理发现提高了药物作用的可能性。对其中一种药片进行了分析,发现其主要成分是双氯芬酸。最初,我们认为IgAN是一个旁观者,因为原发性IgAN是世界上最常见的肾小球肾炎,特别是在亚洲和西班牙裔中。然而,停药后用强的松治疗几天,泌尿系统的检查结果完全消失,6年多来肾脏疾病没有复发,我们推测IgAN也可能是双氯芬酸引发的。结论:我们提出了一例AIN、MCD和IgAN与双氯芬酸伪装成“草药”相关的病例。病因由病理学提出,并通过高分辨率液相色谱质谱检测证实。任何出现NS和AIN症状的患者都应仔细询问非甾体抗炎药的使用史。此外,这是第一例可能由非甾体抗炎药引起的IgAN在随访6年后未复发的报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acute kidney injury and nephrotic syndrome caused by a "magic pill".

Acute kidney injury and nephrotic syndrome caused by a "magic pill".

Introduction: The sudden onset of nephrotic syndrome (NS) and acute interstitial nephritis (AIN) seems to be an uncommon but distinct nonsteroidal anti-inflammatory drug (NSAID)-related renal syndrome.

Case presentation: We present such a case in a patient who took a "magic pill" for gout. Renal biopsy revealed minimal change disease (MCD), acute interstitial nephritis (AIN), severe acute tubular injury (ATI), and IgA nephropathy (IgAN). He was treated with an aborted course of high-dose prednisone, with complete resolution of his renal diseases. The pathologic finding of the combination of MCD and AIN raised the possibility of a drug effect. One of the pills was analyzed and found to be primarily composed of diclofenac. Initially, we considered IgAN a bystander, considering primary IgAN is the most common glomerulonephritis worldwide, especially in Asians and Hispanics. However, the complete resolution of urinary findings after discontinuation of the pill followed by a few days' treatment with prednisone, together with no recurrence of the kidney disease over 6 years, made us speculate that IgAN may have also been triggered by diclofenac.

Conclusion: We presented a case of AIN, MCD, and IgAN associated with diclofenac masquerading as a "herbal" medicine. The cause was suggested by pathology and confirmed with high-resolution liquid chromatography mass spectrometry testing of the pills. A history of NSAID use should be diligently sought in any patient who presents with NS and AIN. In addition, this is the first report of IgAN possibly induced by NSAID without recurrence after 6 years' follow-up.

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