Bilateral Ureteral Stenosis with Hydronephrosis as First Manifestation of Granulomatosis with Polyangiitis (Wegener's Granulomatosis): A Case Report and Review of the Literature.

Case Reports in Nephrology Pub Date : 2020-12-21 eCollection Date: 2020-01-01 DOI:10.1155/2020/7189497
Joelle Suillot, Jürg Bollmann, Samuel Rotman, Eric Descombes
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引用次数: 5

Abstract

Ureteral stenosis is a rare manifestation of granulomatosis with polyangiitis (formerly known as Wegener's granulomatosis). We report the case of a 76-year-old woman with progressive renal failure in which bilateral hydronephrosis due to ureteral stenosis was the first manifestation of the disease. Our patient also had renal involvement with pauci-immune crescentic glomerulonephritis associated with high titers of anti-proteinase 3 c-ANCAs, but no involvement of the upper or lower respiratory tract. The hydronephrosis and renal function rapidly improved under immunosuppressive therapy with high-dose corticosteroids and intravenous pulse cyclophosphamide. We reviewed the literature and found only ten other reported cases of granulomatosis with polyangiitis/Wegener's granulomatosis and intrinsic ureteral stenosis: in two cases, the presenting clinical manifestation was unilateral hydronephrosis and in only two others was the hydronephrosis bilateral, but this complication developed during a relapse of the disease. This case emphasizes the importance of including ANCA-related vasculitis in the differential diagnosis of unusual cases of unilateral or bilateral ureteral stenosis.

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双侧输尿管狭窄伴肾积水为肉芽肿伴多血管炎(韦格纳肉芽肿病)的首发表现:1例报告及文献复习。
输尿管狭窄是肉芽肿合并多血管炎(以前称为韦格纳肉芽肿病)的一种罕见表现。我们报告的情况下,76岁的妇女进行性肾衰竭,其中双侧肾积水由于输尿管狭窄是该病的第一表现。我们的患者也有肾受累与低免疫新月型肾小球肾炎相关的高滴度抗蛋白酶3c - ancas,但没有上呼吸道或下呼吸道受累。在高剂量皮质类固醇和静脉注射环磷酰胺的免疫抑制治疗下,肾积水和肾功能迅速改善。我们回顾了文献,发现只有10例肉芽肿病合并多血管炎/韦格纳肉芽肿病和输尿管狭窄的报道:其中2例临床表现为单侧肾积水,另外2例为双侧肾积水,但这种并发症是在疾病复发期间出现的。本病例强调了将anca相关血管炎纳入单侧或双侧输尿管狭窄异常病例鉴别诊断的重要性。
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来源期刊
Case Reports in Nephrology
Case Reports in Nephrology Medicine-Nephrology
CiteScore
1.70
自引率
0.00%
发文量
32
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