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[韦格纳肉芽肿病——其局限型及诊断与治疗潜力]

[Wegener granulomatosis--its limiting forms and potential of diagnosis and therapy].

作者信息

Liebscher K

出版信息

Z Gesamte Inn Med. 1985 Mar 1;40(5):148-50.

PMID:2859708
Abstract

Apart from the description of the typical clinical symptoms of the Wegener's granulomatosis the author particularly deals with the difficulties of the establishment of the diagnosis and their differential diagnosis. In these cases it is particularly aimed at the differential diagnosis of the primary vasculitides and to the granulomatous diseases in the area of the middle part of the face. For the therapeutic approaches in every case a possibly exact diagnosis is to be demanded. It must be admonished against the fact to begin an immunological therapy already at the suspicion of a Wegener's granulomatosis. The diagnosis must be ascertained either by the proof of organ manifestations (lung, kidney) or by repeated histological confirmation of the diagnosis.

摘要

除了描述韦格纳肉芽肿的典型临床症状外,作者还特别探讨了诊断确立的困难及其鉴别诊断。在这些病例中,特别关注原发性血管炎的鉴别诊断以及面部中部区域的肉芽肿性疾病。对于每种情况的治疗方法,都需要尽可能准确的诊断。必须告诫不要在怀疑韦格纳肉芽肿时就开始免疫治疗。诊断必须通过器官表现(肺、肾)的证据或通过重复的组织学诊断确认来确定。

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