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中枢神经系统肉芽肿性血管炎。病例报告及文献复习。

Granulomatous angitis of the central nervous system. Case report and review.

作者信息

Harrison P E

出版信息

J Neurol Sci. 1976 Oct;29(2-4):335-41. doi: 10.1016/0022-510x(76)90182-9.

Abstract

The nineteenth case report of granulomatous angiitis of the central nervous system is described in a 47-year-old patient, who survived 2 years with his disease. Problems with establishing the diagnosis are discussed. No single group of clinical symptoms or laboratory data exist for making a positive diagnosis during life, although a combination of certain nonspecific factors such as mental change, spinal fluid protein elevation and pleocytosis should be present before the diagnosis of granulomatous angiitis is entertained. Special blood tests and immunological studies and contrast procedures, as well as cortical biopsy have been of little value in establishing the diagnosis; instead, a leptomeningeal biopsy may be the procedure of choice. This patient, as well as the others given a trial of steroid treatment, demonstrated some obvious detectable clinical improvement. All patients treated with steroids have survived longer than any untreated patient suggesting that these drugs may be of some benefit.

摘要

本文描述了第19例中枢神经系统肉芽肿性血管炎病例,患者为一名47岁男性,患病后存活了2年。文中讨论了确诊该病存在的问题。生前确诊尚无单一的临床症状群或实验室数据,不过在考虑诊断肉芽肿性血管炎之前,应出现某些非特异性因素的组合,如精神改变、脑脊液蛋白升高和细胞增多。特殊血液检查、免疫学研究、造影检查以及皮质活检在确诊方面价值不大;相反,软脑膜活检可能是首选方法。该患者以及其他接受类固醇治疗试验的患者,均表现出明显可检测到的临床改善。所有接受类固醇治疗的患者存活时间均长于未接受治疗的患者,这表明这些药物可能有一定益处。

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