Suppr超能文献

[神经结节病。基于截至1963年的537例世界文献病例以及1976 - 1988年病例的临床特征比较分析]

[Neurosarcoidosis. Comparative analysis of the clinical profile based on 537 cases from the world literature up to 1963 and from 1976-1988].

作者信息

Mende D, Suchenwirth R M

机构信息

Neurologische Klinik der Stadt Kassel.

出版信息

Fortschr Neurol Psychiatr. 1990 Jan;58(1):7-18. doi: 10.1055/s-2007-1001166.

Abstract

Observation of neurosarcoidosis in a thirty-year-old black female characterised predominantly by bilateral facial nerve paralysis gave rise to a review of literature since 1978 and also to a comparison with an early study in 1963. As described 1963 the clinical picture is characterized by increased protein content of the CSF (33.8%), facial nerve paresis (25.5%), pleocytosis (23%), diabetes insipidus (21%), hemiparesis (17.2%), organic psychosis (16.9%), papilloedema (15.5%), ataxia (13%), convulsive seizures (12.5%), optic atrophy (12.5%), loss of hearing (12.2%), nystagmus (8.6%) and numerous other symptoms more rarely found. This corresponds to the symptoms of chronic basal meningitis with an infiltration in the neighbouring structures of brain and less frequently the spinal cord. In only 58.7% of the cases (presumably at the onset of sarcoidosis) was the bronchial tract (or the lungs) affected, in 11.5% the skin or the eyes. Although the clinical picture is clear enough the etiology has yet to be determined. Evidence of a pathogen or a pathogenic agent (analogous to berylliosis) has never been established to date. On the other hand there are some indications of a disturbance in the immune system, perhaps of a particular genetic foundation since sarcoidosis strikes black patients with conspicuous frequency. There exist more cases in one family. Exceeding expected random distribution, many patients have the HLA-Factor B 8 (on the chromosome 6) and DR 3. The Kveim-Test was in 71 cases positive, in 12 cases negative. The possibilities of carrying out studies of CSF - analogous to the studies of bronchial lavage - in the most cases of neurosarcoidosis have not been exhausted as to determine the activity of the T-lymphocytes, the interleucines, the angiotensin-converting enzyme while the Gallium 67 scintigraphy and other methods to determine the non-specific activity of the inflammation. The efficiency of the treatment with corticosteroids (Prednison or Triamcinolonacetonid) depends of the phase of the inflammatory process. 12% of the registered cases died.

摘要

一名30岁黑人女性以双侧面神经麻痹为主要特征的神经结节病观察引发了对1978年以来文献的回顾,并与1963年的一项早期研究进行了比较。如1963年所描述的,临床表现的特征为脑脊液蛋白含量增加(33.8%)、面神经麻痹(25.5%)、细胞增多(23%)、尿崩症(21%)、偏瘫(17.2%)、器质性精神病(16.9%)、视乳头水肿(15.5%)、共济失调(13%)、惊厥发作(12.5%)、视神经萎缩(12.5%)、听力丧失(12.2%)、眼球震颤(8.6%)以及许多其他较少见的症状。这与慢性基底脑膜炎的症状相符,伴有脑及较少情况下脊髓邻近结构的浸润。仅58.7%的病例(可能在结节病发病时)支气管(或肺部)受累,11.5%的病例皮肤或眼睛受累。尽管临床表现足够清晰,但病因尚未确定。病原体或致病因子(类似于铍中毒)的证据至今尚未确立。另一方面,有一些迹象表明免疫系统存在紊乱,可能有特定的遗传基础,因为结节病在黑人患者中发病频率显著。一个家族中存在更多病例。超过预期的随机分布,许多患者具有HLA - B8因子(位于6号染色体上)和DR3。Kveim试验在71例中呈阳性,12例中呈阴性。在大多数神经结节病病例中,进行脑脊液研究(类似于支气管灌洗研究)以确定T淋巴细胞、白细胞介素、血管紧张素转换酶的活性以及镓67闪烁扫描和其他确定炎症非特异性活性的方法的可能性尚未穷尽。用皮质类固醇(泼尼松或曲安奈德)治疗的效果取决于炎症过程的阶段。12%的登记病例死亡。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验