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血管炎谱:临床、病理、免疫及治疗方面的考量

The spectrum of vasculitis: clinical, pathologic, immunologic and therapeutic considerations.

作者信息

Fauci A S, Haynes B, Katz P

出版信息

Ann Intern Med. 1978 Nov;89(5 Pt 1):660-76. doi: 10.7326/0003-4819-89-5-660.

Abstract

Vasculitis is a clinicopathologic process characterized by inflammation and necrosis of blood vessels. Certain disorders have vasculitis as the predominant and most obvious manifestation, whereas others have various degrees of vasculitis in association with other primary disorders. Within the entire spectrum of vasculitis virtually any size or type of blood vessel in any organ system can be involved. Most of the vasculitides can be associated directly or indirectly with immunopathogenic mechanisms. In this regard, immune complex mediation is being increasingly recognized as the underlying mechanism in several of the vasculitides. With clinical, pathologic, and immunologic criteria, certain vasculitic disorders can be clearly recognized and categorized as distinct entities, whereas in others there is an overlap of different diseases within a broader category. In recent years, several of the more serious vasculitides, such as Wegener's granulomatosis and the systemic necrotizing vasculitides of the polyarteritis nodosa group, which formerly had extremely poor prognoses, have been shown to be extraordinarily responsive to chronic low-dose cytotoxic therapy, particularly cyclophosphamide.

摘要

血管炎是一种以血管炎症和坏死为特征的临床病理过程。某些疾病以血管炎为主要且最明显的表现,而其他疾病则伴有不同程度的血管炎以及其他原发性疾病。在整个血管炎谱系中,几乎任何器官系统的任何大小或类型的血管都可能受累。大多数血管炎可直接或间接与免疫致病机制相关。在这方面,免疫复合物介导正日益被认为是几种血管炎的潜在机制。根据临床、病理和免疫学标准,某些血管炎疾病可被明确识别并归类为不同的实体,而在其他情况下,在更广泛的类别中不同疾病存在重叠。近年来,一些较严重的血管炎,如韦格纳肉芽肿和结节性多动脉炎组的系统性坏死性血管炎,以前预后极差,但现已证明对慢性低剂量细胞毒性疗法,尤其是环磷酰胺,反应非常良好。

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