DRESS综合征并发急性间质性肾炎并发急性肾盂肾炎1例报道。

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-04-22 eCollection Date: 2025-06-01 DOI:10.1097/MS9.0000000000003318
Nitesh Kumar Karna, Akshyata Osti, Gopal Pokhrel, Neha Karna, Raushan Kumar Thakur, Swikriti Sigdel
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引用次数: 0

摘要

药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)综合征是一种严重的、危及生命的过敏反应,其特征是发热、皮疹、嗜酸性粒细胞增多和多器官受累。肾脏表现,特别是急性间质性肾炎(AIN)是常见的,但在DRESS综合征中同时出现急性肾盂肾炎(APN)和AIN是罕见的,以前也没有文献记载。病例表现:一名19岁女性,表现为发热、呕吐、红疹和面部肿胀。患者有长期使用磺胺吡啶和复方新诺明的病史。实验室检查显示嗜酸性粒细胞增多、肾病综合征和肝酶升高。肾活检表现为APN,临床表现为AIN。根据临床、组织病理学和血清学结果,诊断为DRESS综合征。讨论:DRESS综合征常由磺胺硫氮嗪和复方新诺明等药物引发,可累及多个器官,常见表现为肾脏。虽然AIN是典型的,但该病例突出了并发APN的罕见情况。没有细菌尿和脓尿提示APN的非细菌原因,可能与病毒再激活有关。结论:该病例强调了DRESS综合征合并不典型肾脏受累的谨慎诊断和处理的必要性。它强调了早期发现和停用致病药物的重要性,以及进一步研究了解DRESS综合征复杂肾脏表现的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concurrent acute interstitial nephritis with acute pyelonephritis in DRESS syndrome: a rare case report.

Introduction: Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome is a severe, life-threatening hypersensitivity reaction characterized by fever, rash, eosinophilia, and multi-organ involvement. Renal manifestations, particularly acute interstitial nephritis (AIN), are common, but the concurrent presentation of acute pyelonephritis (APN) with AIN in DRESS syndrome is rare and not previously documented.

Case presentation: A 19-year-old female presented with fever, vomiting, erythematous rash, and facial swelling. She had a history of prolonged use of Sulfasalazine and Cotrimoxazole. Laboratory tests revealed eosinophilia, nephrotic syndrome, and elevated liver enzymes. Renal biopsy showed features of APN, while clinical findings suggested AIN. Based on clinical, histopathological, and serological findings, DRESS syndrome was diagnosed.

Discussion: DRESS syndrome, often triggered by medications like Sulfasalazine and Cotrimoxazole, can involve multiple organs, with renal manifestations being common. While AIN is typical, this case highlights the rare occurrence of concurrent APN. The absence of bacteriuria and pyuria suggests a non-bacterial cause for the APN, possibly related to viral reactivation.

Conclusion: This case underscores the need for careful diagnosis and management of DRESS syndrome with atypical renal involvement. It highlights the importance of early identification and discontinuation of the offending drugs, as well as the necessity for further research to understand the complex renal manifestations in DRESS syndrome.

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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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