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单纯肉芽肿性韦格纳肉芽肿病:一种旧病的新概念。

Purely granulomatous Wegener's granulomatosis: a new concept for an old disease.

作者信息

Boudes P

机构信息

Department of Nephrology, Henri Mondor Hospital, Creteil, France.

出版信息

Semin Arthritis Rheum. 1990 Jun;19(6):365-70. doi: 10.1016/0049-0172(90)90073-o.

Abstract

In summary, PGWG corresponds to an early phase of WG, presenting only with extravascular granuloma. Primarily, ENT, eye, or lung tissues are involved, but any organ may be affected. The diagnosis is made by typical palisading granuloma associated with elevated c-ANCA levels in the patients' serum. The concept of an early granulomatous lesion (PGWG) facilitates the early diagnosis of WG and leads to classification of different forms of disease according to the multistep evolution hypothesis: first PGWG, then localized or limited forms of the disease, and ultimately generalized vasculitis with renal involvement (classical WG). The concept of PGWG forms the basis for future therapeutic trials where folate antagonists are restricted to PGWG, while immunosuppressive treatment is required for the other stages of WG.

摘要

总之,PGWG相当于WG的早期阶段,仅表现为血管外肉芽肿。主要累及耳鼻喉、眼或肺组织,但任何器官都可能受累。诊断依据为患者血清中与c-ANCA水平升高相关的典型栅栏状肉芽肿。早期肉芽肿性病变(PGWG)的概念有助于WG的早期诊断,并根据多步演变假说对不同形式的疾病进行分类:首先是PGWG,然后是疾病的局限性或有限形式,最终是累及肾脏的全身性血管炎(经典WG)。PGWG的概念构成了未来治疗试验的基础,在这些试验中,叶酸拮抗剂仅限于PGWG使用,而WG的其他阶段则需要免疫抑制治疗。

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