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控制并发于克罗恩病的淀粉样变性:一项临床病理研究。

Control of AA amyloidosis complicating Crohn's disease: a clinico-pathological study.

机构信息

Department of Gastroenterology, St. Luc University Hospital, Brussels, Belgium.

出版信息

Eur J Clin Invest. 2013 Mar;43(3):292-301. doi: 10.1111/eci.12045. Epub 2013 Feb 4.

Abstract

BACKGROUND

Immunosuppressive drugs may prevent or partially reverse progression of renal AA-amyloidosis, a rare complication of Crohn's disease, often fatal due to renal failure.

MATERIALS AND METHODS

The clinical, biological and pathological data of 16 patients treated since 1976 were reviewed. Serum amyloid A was determined in surviving patients.

RESULTS

The median age of the 16 patients (13 men) was 23·5 years (range 16-69). At Crohn's disease onset, Montreal phenotypes were similar to reported data. Out of 15 patients with renal insufficiency, 8 developed a nephrotic syndrome and 7 a low grade proteinuria. The single patient without renal insufficiency had nephrotic syndrome. A significant correlation (P < 0·05) between the extension of renal amyloid A and sclerosis was found in 12 patients. One patient had a 10 year remission of nephrotic syndrome with immunosuppressive drugs. In 6 patients treated with anti-TNF-α (Tumor-Necrosis-Factor-α) agents, anaphylactic reaction (1/6), death from septic shock (1/6), 5-year remission (1/6) or reduction of nephrotic syndrome (1/6) and stabilization of renal insufficiency (2/6) were observed. Surgery was performed in 10 patients. Kidney transplantation was performed in 5 of the 8 patients dialysed for end-stage renal failure. Among 6/16 patients (37%) still alive, 3 belong to the 5 transplanted patients (survival: 3-20 years) and 3 to the anti-TNF-α drugs treated patients; all but one exhibited a low serum amyloid A level.

CONCLUSIONS

Suppression of Crohn's disease inflammation potentially leads to the control of amyloid A production, assessed by a decrease of serum amyloid A. Kidney transplantation provides a long survival.

摘要

背景

免疫抑制剂可能预防或部分逆转肾 AA 淀粉样变性的进展,这是克罗恩病的罕见并发症,常因肾衰竭而致命。

材料和方法

回顾了自 1976 年以来治疗的 16 例患者的临床、生物学和病理学数据。对存活患者进行了血清淀粉样蛋白 A 测定。

结果

16 例患者(13 名男性)的中位年龄为 23.5 岁(范围 16-69 岁)。在克罗恩病发病时,蒙特利尔表型与报告数据相似。在 15 例肾功能不全患者中,8 例出现肾病综合征,7 例出现轻度蛋白尿。唯一无肾功能不全的患者出现肾病综合征。在 12 例患者中发现肾淀粉样 A 与硬化的扩展存在显著相关性(P<0.05)。1 例患者经免疫抑制剂治疗肾病综合征缓解 10 年。在 6 例接受抗 TNF-α(肿瘤坏死因子-α)治疗的患者中,观察到过敏反应(1/6)、脓毒性休克死亡(1/6)、5 年缓解(1/6)、肾病综合征减少(1/6)和肾功能不全稳定(2/6)。10 例患者进行了手术。5 例因终末期肾衰竭透析的患者进行了肾移植。在 16 例仍存活的患者中(37%),3 例属于 5 例移植患者(存活:3-20 年),3 例属于抗 TNF-α药物治疗患者;除 1 例外,所有患者血清淀粉样蛋白 A 水平均较低。

结论

抑制克罗恩病炎症可能会导致淀粉样蛋白 A 产生的控制,通过降低血清淀粉样蛋白 A 来评估。肾移植提供了长期生存。

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