ISSN 1006-298X      CN 32-1425/R

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肾脏病与透析肾移植杂志 ›› 2018, Vol. 27 ›› Issue (3): 208-213.DOI: 10.3969/j.issn.1006-298X.2018.03.002

• 论文 • 上一篇    下一篇

单纯C3沉积的感染后肾小球肾炎与C3肾小球肾炎比较

  

  • 出版日期:2018-06-28 发布日期:2018-06-29

Comparison of postinfectious glomerulonephritis with isolated C3 deposition and C3 glomerulonephritis

  • Online:2018-06-28 Published:2018-06-29

摘要:

目的:分析单纯C3沉积的感染后肾小球肾炎(C3PIGN)的临床、病理和肾脏预后特点,并和C3肾小球肾炎(C3GN)进行比较。
方法:回顾性分析2009年至2015行肾活检诊断为感染后肾小球肾炎(PIGN)和C3肾小球肾炎(C3GN)患者的临床、病理及随访资料,分别对C3PIGN和免疫球蛋白合并补体沉积的感染后肾小球肾炎(Ig+C3PIGN)、C3PIGN和C3肾小球肾炎(C3GN)的患者进行比较。
结果:(1)共纳入89例PIGN和52例C3GN,PIGN患者中43例(483%)为C3PIGN,46例(517%)Ig+C3PIGN。(2)与Ig+C3PIGN相比,C3PIGN肾病范围的蛋白尿和低白蛋白血症比例、新月体比例、肾小管萎缩间质纤维化(IFTA)的比例及系膜区和内皮下的电子致密物沉积的比例较低。(3)与C3GN比较,C3PIGN患者未成年人比例更高,病程更短,尿红细胞计数更多,肾病范围蛋白尿比例和低白蛋白血症发生率更低;C3PIGN患者球性硬化、IFTA、动脉透明变性、肾小球系膜区和内皮下电子致密物沉积的比例更低,而驼峰比例更高。C3PIGN和C3GN患者肾小球均存在C3b、C3c和C3g沉积。(4)C3PIGN患者的临床转归总体预后良好,39例患者随访>1年,其中32例患者1年内尿检转阴,7例患者尿检持续阳性>1年,其中5例患者尿检逐渐转阴,而2例患者尿检持续不缓解,提示可能存在补体旁路途径活化失衡,符合C3GN的诊断。
结论:与Ig+C3PIGN和C3GN相比,C3PIGN的临床和组织形态学病变较轻,但是C3PIGN和C3GN肾小球内有相同的补体片段沉积,提示两者肾小球局部的补体活化和裂解失活过程有相似之处。对C3PIGN患者要进行长期追踪随访,以便发现这些以感染为诱因,临床诊断为“C3PIGN”,而实际是C3GN患者。

关键词: 单纯C3沉积, 感染后肾小球肾炎, C3肾小球肾炎, 肾脏病理, 补体片段

Abstract:

Objective:To analyze clinicopathological and renal prognostic features of postinfectious glomerulonephritis with isolated C3 deposition(C3PIGN).
Methodology:postinfectious glomerulonephritis(PIGN)and C3 glomerulonephritis(C3GN)diagnosed by renal biopsy from 2009 to 2015 were enrolled in this study.
Results:(1)43 cases of PIGN with C3 deposition(C3PIGN),46 cases of PIGN with Ig and C3 deposition(Ig+C3PIGN)and 52 cases of C3GN were included in this study.(2)In comparison with Ig+C3PIGN,C3PIGN group has lower rates of nephrotic range proteinuria,hypoalbuminemia,crescents,tubular atrophic interstitial fibrosis(IFTA),mesangial and subendothelial electron dense deposits.(3)In comparison with C3GN,C3PIGN group has higher proportion of children,shorter duration of disease,higher rates of microscopic hematuria and lower rates of nephrotic range proteinuria and hypoalbuminemia.The proportion of global sclerosis,IFTA,hyaline degeneration of arteries and mesangial and subendothelial electron dense deposits were lower in C3PIGN group.However,There were no differences in complement C3 fragment deposition between two groups.(4)32 patients with C3PIGN recovered completely within 1 year and 7 patients presented with persistented proteinuria and/or hematuria,among which 5 patients gradually turned negative,while 2 patients did not go to remission,suggesting that there is an imbalance in the alternative pathway of complement activation,consistent with the diagnosis of C3GN.
Conclusion:
Compared with Ig+C3PIGN and C3GN,the clinical and histopathological changes of C3PIGN were mild,but the same C3 fragment was deposited in glomeruli of both C3PIGN and C3GN.Longterm followup of patients with C3PIGN should be performed in order to detect C3GN patients who are clinically diagnosed as “C3PIGN” with infection as the cause.