Membranoproliferative Glomerulonephritis Type 1 Secondary to an Infected Ventriculoperitoneal Shunt: a Case Report

Christos Paliouras, Foteini Lamprianou, Georgios Ntetskas, Georgios Mattas, N. Karvouniaris, G. Aperis, P. Alivanis
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引用次数: 2

Abstract

Abstract Ventricular shunting is the usual method for treatment of congenital or acquired hydrocephalus. Immune-mediated glomerulonephritis (shunt nephritis) is a rare but life-threatening complication of this neurosurgical technique. Intraglomerular deposition of circulating immune complexes and the subsequent activation of the classical pathway of serum complement’s cascade result in glomerular inflammation. Membranoproliferative gomerulonephritis is the most common histologic pattern observed in renal biopsy. The diagnosis needs high suspicion and is based on clinical and laboratory findings. Deterioration of renal function in association with signs of infection and low levels of serum complement’s proteins C3 and C4 make the diagnosis possible. The prognosis is variable and depends on the time of diagnosis after the onset of glomerular injury. The optimal treatment includes timely removal of the infected shunt in combination with aggressive antibiotic therapy. In this paper we present the case of a membranoproliferative glomerulonephritis type 1 in a patient with a ventriculoperitoneal shunt. Although this type of shunting is considered safer than the ventriculoatrial one, the risk of complications such as an immune-mediated glomerulonephritis still exists.
1型膜增生性肾小球肾炎继发于感染的脑室-腹膜分流:1例报告
摘要脑室分流术是治疗先天性或后天性脑积水的常用方法。免疫介导的肾小球肾炎(分流性肾炎)是这种神经外科技术罕见但危及生命的并发症。肾小球内循环免疫复合物的沉积和随后的血清补体级联经典途径的激活导致肾小球炎症。膜增生性肾小球肾炎是肾活检中最常见的组织学类型。诊断需要高度怀疑,并以临床和实验室结果为基础。肾功能恶化与感染体征和血清补体蛋白C3和C4低水平相关,使诊断成为可能。预后是可变的,取决于肾小球损伤发生后的诊断时间。最佳的治疗方法包括及时切除受感染的分流管并结合积极的抗生素治疗。在这篇论文中,我们提出一个病例膜增生性肾小球肾炎1型患者与脑室腹腔分流。尽管这种分流被认为比心室房分流更安全,但仍然存在并发症的风险,如免疫介导的肾小球肾炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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