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一名患有特发性肾病综合征的儿童发生药物性间质性肾炎。

Drug-induced interstitial nephritis in a child with idiopathic nephrotic syndrome.

作者信息

Printza Nikoleta, Koukourgianni Fotini, Saleh Thaer, Goga Chrissa, Papachristou Fotis

机构信息

1st Pediatric Department, Aristotles University, Hippokration General Hospital, Konstantinoupoleos, Thessaloniki, Greece.

出版信息

Saudi J Kidney Dis Transpl. 2009 Nov;20(6):1072-5.

Abstract

Acute renal failure (ARF) is a rare but severe complication of active idiopathic nephrotic syndrome (INS) in children. It may be due to several causes with different outcomes. Both the clinical picture of the patient as well as laboratory, imaging and histopathological findings may help in the diagnosis. We present a case of drug-induced acute interstitial nephritis (AIN), complicated with ARF, in a 2(1/2) -year-old girl with active INS. The child was referred to the Hippokration General Hospital, Thessaloniki, Greece hospital with steroid-resistant NS; renal biopsy was performed, which did not show any remarkable findings and cyclosporine was administered in addition to steroid therapy. The first day after biopsy, the child developed gross hematuria and abdominal pain and an antibiotic was added to her treatment. In the following days, fever, vomiting, hypertension and ARF occurred. Ultrasound study revealed enlarged kidneys with increased echogenity and loss of corticomedullary differentiation. The antibiotic and cyclosporine were stopped and the child was managed with furosemide, nifedipine and steroids. A second renal biopsy was performed, which confirmed the diagnosis of acute interstitial nephritis. The child did not require dialysis therapy. Her urine output improved gradually and the serum creatinine normalized one month after the initial episode. Our case re-emphasizes the need for investigation of factors precipitating ARF in children with idiopathic NS.

摘要

急性肾衰竭(ARF)是儿童活动性特发性肾病综合征(INS)罕见但严重的并发症。其病因可能有多种,预后也各不相同。患者的临床表现以及实验室、影像学和组织病理学检查结果均有助于诊断。我们报告一例2岁半患有活动性INS的女孩发生药物性急性间质性肾炎(AIN)并并发ARF的病例。该患儿因激素抵抗性肾病被转诊至希腊塞萨洛尼基的希波克拉底综合医院;进行了肾活检,未发现任何显著异常,除激素治疗外还给予了环孢素。肾活检后第一天,患儿出现肉眼血尿和腹痛,治疗中加用了一种抗生素。在接下来的几天里,患儿出现发热、呕吐、高血压和ARF。超声检查显示肾脏增大,回声增强,皮髓质分界不清。停用抗生素和环孢素,患儿接受呋塞米、硝苯地平和激素治疗。进行了第二次肾活检,确诊为急性间质性肾炎。患儿无需透析治疗。其尿量逐渐改善,血清肌酐在初次发病后一个月恢复正常。我们的病例再次强调了对特发性肾病患儿急性肾衰竭诱发因素进行调查的必要性。

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