局灶节段性肾小球硬化与交叉融合肾异位的关联:继发性局灶节段性肾小球硬化的新病因还是偶然关联?

Rosielly Melo Tavares, Yasmin Silva e Sousa, Ginivaldo Victor Ribeiro do Nascimento
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引用次数: 0

摘要

交叉融合肾异位是一种罕见的先天性肾脏异常。它可与肾盂输尿管梗阻、膀胱输尿管反流和多囊发育不良相关,有时可导致肾结石和反复尿路感染。然而,与肾小球病变相关的并发症在先天性肾异常患者中是罕见的。在此,我们报告一例交叉融合肾异位合并局灶节段性肾小球硬化(FSGS)。初步临床结果提示继发性FSGS的可能性;尽管如此,免疫抑制还是成功完成了。该病例在无症状患者中显示了从未报道过的关联。世界肾癌杂志,2015;4(1):183-185 doi: http://dx.doi.org/10.14740/wjnu207w
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between Focal Segmental Glomerulosclerosis and Cross-Fused Renalectopia: A New Cause of Secondary Focal Segmental Glomerulosclerosis or a Casual Association?
Cross-fused renal ectopia is a rarely described congenital kidney anomaly. It can occur in association with ureteropelvic obstruction, vesicoureteral reflux, and multicystic dysplasia, which sometimes leads to nephrolithiasis and recurrent urinary infection. However, complications related to glomerulopathies are rare in patients with congenital kidney anomaly. Here, we report a case of cross-fused renal ectopia associated with focal segmental glomerulosclerosis (FSGS). The initial clinical findings suggested the possibility of secondary FSGS; nonetheless immunosuppression was successfully done. The case demonstrates a never-before reported association in an asymptomatic patient. World J Nephrol Urol. 2015;4(1):183-185 doi: http://dx.doi.org/10.14740/wjnu207w
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