New Evidence-Based Treatment Approach in Behçet's Disease.

Pathology research international Pub Date : 2012-01-01 Epub Date: 2011-10-05 DOI:10.1155/2012/871019
Erkan Alpsoy
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引用次数: 47

Abstract

Behçet's disease (BD) is a chronic, relapsing, and debilitating systemic vasculitis of unknown aetiology with the clinical features of mucocutaneous lesions, ocular, vascular, articular, neurologic, gastrointestinal, urogenital, and pulmonary involvement. The disease is much more frequent along the ancient “Silk Route” extending from Eastern Asia to the Mediterranean basin, compared with Western countries. The disease usually starts around the third or fourth decade of life. Male sex and a younger age of onset are associated with more severe disease. Although the treatment has become much more effective in recent years, BD is still associated with severe morbidity and considerable mortality. The main aim of the treatment should be the prevention of irreversible organ damage. Therefore, close monitoring, early, and appropriate treatment is mandatory to reduce morbidity and mortality. The treatment is mainly based on the suppression of inflammatory attacks of the disease using immunomodulatory and immunosuppressive agents. In this paper, current state of knowledge regarding the therapeutic approaches is outlined. To provide a rational framework for selecting the appropriate therapy along the various treatment choices, a stepwise, symptom-based, evidence-based algorithmic approach was developed.
behaperet病循证治疗新途径
behet病(BD)是一种病因不明的慢性、复发性、衰弱性全身性血管炎,临床特征为皮肤粘膜病变、眼部、血管、关节、神经、胃肠道、泌尿生殖系统和肺部受累。与西方国家相比,这种疾病在从东亚延伸到地中海盆地的古代“丝绸之路”沿线更为频繁。这种疾病通常在生命的第三或第四个十年左右开始。男性和较年轻的发病年龄与更严重的疾病有关。虽然近年来治疗已经变得更加有效,但双相障碍仍然与严重的发病率和相当高的死亡率有关。治疗的主要目的应该是防止不可逆的器官损害。因此,密切监测、早期和适当治疗是降低发病率和死亡率的必要措施。治疗主要基于使用免疫调节剂和免疫抑制剂抑制疾病的炎症发作。本文概述了目前有关治疗方法的知识状况。为了提供一个合理的框架,以便在各种治疗选择中选择适当的治疗方法,我们开发了一种逐步的、基于症状的、基于证据的算法方法。
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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