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一种“神药”引发的急性肾损伤和肾病综合征。

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

作者信息

Cao Yangming, Phan Thao, Armenian Patil, Zuckerman Jonathan E

机构信息

Division of Nephrology, Department of Internal Medicine, UCSF Fresno.

The Nephrology Group, Fresno.

出版信息

Clin Nephrol Case Stud. 2025 Sep 4;13:59-65. doi: 10.5414/CNCS111804. eCollection 2025.

Abstract

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.

摘要

引言

肾病综合征(NS)和急性间质性肾炎(AIN)的突然发作似乎是一种罕见但独特的与非甾体抗炎药(NSAID)相关的肾综合征。

病例报告

我们报告了一名服用“神药”治疗痛风的患者出现这种情况。肾活检显示微小病变性肾病(MCD)、急性间质性肾炎(AIN)、严重急性肾小管损伤(ATI)和IgA肾病(IgAN)。他接受了一个疗程中断的大剂量泼尼松治疗,肾脏疾病完全缓解。MCD和AIN合并的病理发现增加了药物作用的可能性。对其中一粒药丸进行分析,发现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是全球最常见的肾小球肾炎,尤其是在亚洲人和西班牙裔中。然而,停药后经泼尼松治疗数天,尿液检查结果完全缓解,且6年多来肾病未复发,这使我们推测IgAN也可能是由双氯芬酸引发的。

结论

我们报告了一例与伪装成“草药”的双氯芬酸相关的AIN、MCD和IgAN病例。病因由病理学提示,并通过对药丸的高分辨率液相色谱质谱测试得到证实。对于任何出现NS和AIN的患者,都应仔细询问NSAID使用史。此外,这是首例NSAID诱导的IgAN在随访6年后无复发的报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ff8/12444431/60cd402e674b/CNCS-13-059-01.jpg

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