Inflammatory abdominal aortic aneurysm and retroperitoneal fibrosis

Mihailo Nešković, Nenad Đukić, A. Rakic, Đ. Radak
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Abstract

The inflammatory aneurysm of abdominal aorta (IAAA) accounts for 3-11% of all abdominal aortic aneurysms, and occurs predominantly in men. It has similar pathological mechanisms like idiopathic retroperitoneal fibrosis (IRF) and perianeurysmal retroperitoneal fibrosis (PRF), thus presenting the same non-specific systemic inflammatory disorder known as chronic periaortitis (CP). Recognition of CP early in its course is important in order to reduce morbidity due to complications, such as renal failure and mortality from aortic rupture. However, the initial symptoms of CP are non-specific, which makes early clinical diagnosis extremely difficult. Various studies have shown favorable outcomes following corticosteroid treatment in nearly 90% of patients. The positive effects of adding different immunosuppressants to corticoid therapy have established such "duo-therapy" as a durable treatment option. Also, cessation of smoking has a positive effect on disease course and it should be an integral part of every treatment regimen. Operative repair of the abdominal aortic aneurysm is considered to be the definitive treatment for IAAA. The effects of both open and endovascular interventions on the inflammatory component however remain unclear. Resolution of periaortic fibrotic tissue after surgery for IAAA is still debated. Some investigators have reported a complete resolution while the others have noted partial regression and even persistence of the inflammatory cuff. Current treatment strategies are based upon "the best available evidence'', mostly derived from clinical experience obtained by case series involving a small number of patients. Studies of a higher evidence level are very much needed to adjust our approach to such patients and to establish guidelines for treating this complex and serious disorder.
炎性腹主动脉瘤和腹膜后纤维化
腹主动脉炎症性动脉瘤(IAAA)占所有腹主动脉瘤的3-11%,多见于男性。它具有与特发性腹膜后纤维化(IRF)和动脉瘤周围腹膜后纤维化(PRF)相似的病理机制,因此表现为相同的非特异性全身性炎症,称为慢性主动脉周围炎(CP)。为了减少并发症的发病率,如肾衰竭和主动脉破裂引起的死亡率,在病程早期识别CP是很重要的。然而,CP的初始症状是非特异性的,这使得早期临床诊断非常困难。各种研究表明,近90%的患者接受皮质类固醇治疗后预后良好。在皮质激素治疗中加入不同免疫抑制剂的积极作用已经确立了这种“双重治疗”作为一种持久的治疗选择。此外,戒烟对病程有积极的影响,它应该是每一个治疗方案的组成部分。腹主动脉瘤的手术修复被认为是IAAA的最终治疗方法。然而,开放和血管内干预对炎症成分的影响尚不清楚。IAAA术后主动脉周围纤维化组织的溶解仍有争议。一些研究人员报告了完全解决,而另一些则注意到部分消退,甚至炎性袖带的持续存在。目前的治疗策略基于“可获得的最佳证据”,这些证据大多来自于通过涉及少数患者的病例系列获得的临床经验。非常需要更高证据水平的研究来调整我们对这类患者的治疗方法,并为治疗这种复杂而严重的疾病建立指导方针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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