Severe acute kidney injury induced by crescentic glomerulonephritis in a child with infective endocarditis.

IF 0.8 4区 医学 Q4 PEDIATRICS
Neslihan Yılmaz, Selçuk Yüksel, Dolunay Gürses, İlknur Girişgen, Tülay Becerir, Münevver Yılmaz, Furkan Ufuk, Gülsün Gülten
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引用次数: 0

Abstract

Background: Kidney involvement related to infective endocarditis (IE) may present with different clinical findings. The most common histopathological finding of renal involvement is a combination of proliferative and exudative glomerulonephritis. However, severe acute kidney injury (AKI) induced by crescentic glomerulonephritis (CGN) is extremely rare in children with IE. To date, only 4 pediatric cases with IE-induced CGN had been reported. We present a 14-year old girl with IE-induced CGN.

Case: A 14-year old girl with fever, macroscopic hematuria, oliguria, and acute kidney injury (AKI) was admitted to our clinic. The medical history revealed that the patient had undergone several cardiac interventions due to truncus arteriosus type 1, and she recovered from IE-induced glomerulonephritis following antibiotherapy six months ago. During admission, the patient was diagnosed with IE according to one major (positive imaging finding) and three minor (fever, predisposing cardiac disease, and immunological criterion) criteria. Immediate antibiotic treatment was initiated. A kidney biopsy was performed, which showed crescentic glomerulonephritis (CGN with crescents, > 50%). Daily pulse steroid (3 days), monthly pulse cyclophosphamide (6 doses), and oral steroid (2 mg/kg/day) therapy were initiated with gradual dose tapering. The patient underwent 12 hemodialysis sessions until the 38 < sup > th < /sup > day of the treatment. She was discharged on the 45th day of treatment with normal kidney function tests and negative acute phase reactants. Treatment was maintained with mycophenolate mofetil (MMF) after a 6-month course of cyclophosphamide. MMF was discontinued in the 12th month. At the 18thmonth follow-up visit the patient had mild proteinuria, and was on ramipril therapy.

Conclusions: The occurrence of CGN should be considered in children with predisposing cardiac disease, who develop hematuria, proteinuria, and severe AKI. Although antibiotic therapy alone is often sufficient in this immune complex GN induced by infection, early initiation of additional immunosuppressive therapy in the presence of CGN may be beneficial for long term preservation of kidney functions.

传染性心内膜炎患儿月牙性肾小球肾炎致严重急性肾损伤1例。
背景:与感染性心内膜炎(IE)相关的肾脏受累可能有不同的临床表现。肾脏受累最常见的组织病理学表现是增生性和渗出性肾小球肾炎的结合。然而,月牙状肾小球肾炎(CGN)引起的严重急性肾损伤(AKI)在IE患儿中极为罕见。迄今为止,仅报道了4例ie诱导的儿童CGN。我们报告一名14岁的女孩患有ie诱发的CGN。病例:一名14岁女童因发热、肉眼可见血尿、少尿并急性肾损伤(AKI)住院。病史显示,患者因1型动脉干接受过多次心脏介入治疗,6个月前经抗生素治疗后从ie性肾小球肾炎中恢复。入院时,患者根据1项主要(影像学阳性发现)和3项次要(发热、易患心脏疾病和免疫标准)诊断为IE。立即开始抗生素治疗。行肾活检,示新月形肾小球肾炎(CGN with crescent, >50%)。每日脉冲类固醇(3天),每月脉冲环磷酰胺(6次剂量)和口服类固醇(2 mg/kg/天)治疗开始,剂量逐渐减少。患者接受了12次血液透析,直到38岁。吃晚饭在th & lt;/一口比;治疗当天。患者治疗第45天出院,肾功能检查正常,急性期反应物阴性。在环磷酰胺治疗6个月后,继续使用霉酚酸酯(MMF)治疗。MMF在第12个月停止使用。在18个月的随访中,患者有轻度蛋白尿,并接受雷米普利治疗。结论:发生血尿、蛋白尿和严重AKI的易感心脏病患儿应考虑CGN的发生。虽然对于感染引起的免疫复合物GN,单独使用抗生素治疗通常是足够的,但在存在CGN的情况下,早期开始额外的免疫抑制治疗可能有利于肾功能的长期保存。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
122
审稿时长
6-12 weeks
期刊介绍: The Turkish Journal of Pediatrics is a multidisciplinary, peer reviewed, open access journal that seeks to publish research to advance the field of Pediatrics. The Journal publishes original articles, case reports, review of the literature, short communications, clinicopathological exercises and letter to the editor in the field of pediatrics. Articles published in this journal are evaluated in an independent and unbiased, double blinded peer-reviewed fashion by an advisory committee.
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