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首页> 外文期刊>BMC Nephrology >Regional secondary focal segmental glomerulosclerosis in a transplanted kidney – resolution with treatment of a segmental renal artery stenosis
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Regional secondary focal segmental glomerulosclerosis in a transplanted kidney – resolution with treatment of a segmental renal artery stenosis

机译:移植肾中的区域性继发性局灶性节段性肾小球硬化-通过治疗节段性肾动脉狭窄来解决

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Background Conditions associated with high intraglomerular filtration pressure can cause secondary focal segmental glomerulosclerosis (FSGS). Unilateral renal artery stenosis (RAS) or its occlusion results in FSGS-like changes and the nephrotic syndrome in the contralateral kidney due to hyperfiltration. However, it has been rarely reported that stenosis of a renal arterial branch can result in FSGS-like changes in a different portion in the same kidney allograft. Case presentation A 60-year-old male kidney recipient developed allograft dysfunction after angiotensin II receptor blockade for hypertension 4?months after transplantation. It was proven that one of two arterial branches of the graft was markedly stenotic. Graft dysfunction improved after percutaneous transluminal arterioplasty (PTA), however; the stenosis recurred and massive proteinuria developed 5?months later. Graft biopsy showed ischemic changes in the region fed by the stenotic artery branch and in contrast FSGS-like changes in the region fed by the other branch. His clinicopathological manifestation including massive proteinuria almost normalized after the repeat PTA. Conclusion Here we report a case of secondary FSGS of a kidney allograft due to severe RAS of a branch of the same kidney, in which clinical and pathological improvement were confirmed after radiological intervention. When moderate to severe proteinuria appear, secondarily developed FSGS as well as primary (recurrent or de novo) FSGS should be taken into account in kidney transplant recipients.
机译:背景与高肾小球内滤过压相关的疾病可导致继发性局灶性节段性肾小球硬化(FSGS)。由于超滤作用,单侧肾动脉狭窄(RAS)或其闭塞会导致FSGS样变化和对侧肾脏的肾病综合征。然而,极少有报道说肾动脉分支狭窄会导致同一肾脏同种异体移植的不同部位出现FSGS样变化。病例介绍一名60岁男性肾脏接受者在移植后4个月因血管紧张素II受体阻滞治疗高血压而出现同种异体移植功能障碍。事实证明,移植物的两个动脉分支之一明显狭窄。经皮腔内动脉成形术(PTA)后,移植物功能障碍得到改善。狭窄复发,5个月后出现大量蛋白尿。移植物活检显示狭窄动脉分支馈送区域的缺血性改变,而另一分支分支馈送区域的FSGS样变化。重复PTA后,他的临床病理表现包括大量蛋白尿几乎恢复正常。结论在这里,我们报道了由于同一个肾脏分支的严重RAS导致的同种异体肾继发性FSGS病例,在放射干预后证实了临床和病理上的改善。当出现中度至重度蛋白尿时,肾移植接受者应考虑继发性FSGS以及原发性(复发性或从头开始)FSGS。

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