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Renal granulomatoses: a retrospective study of 40 cases and review of the literature.

机译:肾肉芽肿病:回顾性研究40例和文献复习。

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Renal granulomatoses represent 0.5%-0.9% of nephropathies examined by renal biopsies. Granulomas can be isolated to the kidney or associated with other tissue involvement. We describe 40 consecutive patients with renal granulomatoses, associated with pauci-immune crescentic glomerulonephritis in 2 patients and with vasculitis in another, seen in northeastern Paris hospitals between January 1991 and February 2004. The criterion for inclusion was the presence of 1 or more epithelioid granulomas in the renal interstitium. Our population of 25 men and 15 women had a median age of 53 years. All patients suffered from renal insufficiency with median creatininemia of 236.8 micromol/L (range, 124-805 micromol/L), associated with hypertension (25%), median proteinuria of 0.6 g/24 h (range, 0.08-3.00 g/24 h), microscopic hematuria (15%) and leukocyturia (22.5%). Histologic examination of extrarenal specimens detected granulomas in 82.4% of the bronchial biopsies taken, and in 100% of the 2 skin biopsies, the 2 lymph-node biopsies, and the liver and colon biopsies. The following etiologies were retained: sarcoidosis for 20 (50%) patients, drug-induced for 7 (17.5%), tuberculosis for 3 (7.5%), Wegener granulomatosis for 2 (5%), and leprosy, Mycobacterium avium infection, and Crohn disease for 1 (2.5%) patient each. No etiology could be identified for 5 (12.5%) patients. Treatment must be adapted to the etiology of each case. The renal outcome after treatment was generally favorable, with the estimated median creatinine clearance increasing from 26 mL/min (range, 5.4-80.0 mL/min) to 46.5 mL/min (range, 0-118 mL/min) after a median follow-up of 35.5 months (range, 3-158 mo). Nonetheless, 32 patients had persistent renal insufficiency; 1 required hemodialysis and another underwent renal transplantation. Sarcoidosis and medications are the most common causes of renal granulomatosis. Idiopathic and drug-induced forms do not relapse after treatment discontinuation, and remission persists at long-term follow-up.
机译:肾肉芽肿病占肾活检检查肾病的0.5%-0.9%。肉芽肿可分离到肾脏或与其他组织累及相关。我们描述了1991年1月至2004年2月在巴黎东北医院见到的40例连续性肾肉芽肿患者,其中2例患者伴有弱免疫性新月体性肾小球肾炎,另一例患者患有脉管炎。纳入标准为存在1个或多个上皮样肉芽肿。在肾间质中。我们的25名男性和15名女性人口的平均年龄为53岁。所有患者均患有肾功能不全,其中肌酐水平中位数为236.8 micromol / L(范围124-805 micromol / L),伴有高血压(25%),蛋白尿中位数为0.6 g / 24 h(范围0.08-3.00 g / 24) h),镜下血尿(15%)和白细胞尿(22.5%)。肾外标本的组织学检查在82.4%的支气管活检中以及100%的2个皮肤活检,2个淋巴结活检以及肝和结肠活检中检测到肉芽肿。保留以下病因:结节病20例(50%),药物诱发7例(17.5%),结核3例(7.5%),韦格纳肉芽肿2例(5%),麻风病,鸟分枝杆菌感染和每个患者中有1名(2.5%)患者患有克罗恩病。无法确定5位(12.5%)患者的病因。治疗方法必须适合每种情况的病因。治疗后肾脏预后总体良好,估计中位肌酐清除率从26 mL / min(范围:5.4-80.0 mL / min)增加到46.5 mL / min(范围:0-118 mL / min)。 -35.5个月(范围3-158 mo)。尽管如此,仍有32例患者持续存在肾功能不全。 1例需要血液透析,另一例接受肾移植。结节病和药物治疗是肾肉芽肿的最常见原因。特发性和药物引起的形式在治疗中止后不会复发,并且在长期随访中仍可缓解。

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