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淀粉样β蛋白相关血管炎:与脑淀粉样血管病相关的中枢神经系统原发性血管炎。

Abeta-related angiitis: primary angiitis of the central nervous system associated with cerebral amyloid angiopathy.

作者信息

Scolding Neil J, Joseph Fady, Kirby Patricia A, Mazanti Ingrid, Gray Françoise, Mikol Jacqueline, Ellison David, Hilton David A, Williams Timothy L, MacKenzie James M, Xuereb John H, Love Seth

机构信息

Department of Neurology, Institute of Clinical Neurosciences, University of Bristol, Frenchay Hospital, Bristol, UK.

出版信息

Brain. 2005 Mar;128(Pt 3):500-15. doi: 10.1093/brain/awh379. Epub 2005 Jan 19.

Abstract

Idiopathic or primary angiitis of the CNS (PACNS) and cerebral amyloid angiopathy (CAA) are unusual vasculopathies generally regarded as unrelated disorders. A few case reports have, however, described granulomatous angiitis in patients with sporadic, amyloid beta peptide (Abeta)-related CAA. Here we describe the clinical, neuroradiological and neuropathological features of nine patients with Abeta-related angiitis (ABRA). Combining these with the individual case reports drawn from the literature has allowed us to define ABRA as a clinical entity and to compare its features with those of PACNS. The mean age of presentation of ABRA (67 years) is higher than that of PACNS but lower than that of sporadic non-inflammatory Abeta-related CAA. Alterations in mental status (59%), headaches (35%), seizures and focal neurological deficits (24%) are common. Hallucinations are a presenting manifestation in 12% of cases. Most patients have white matter hyperintensities on MRI but these are of similar appearance to those in PACNS. Cerebrospinal fluid usually shows modest elevation of protein and pleocytosis. Neuropathology reveals angiodestructive inflammation, often granulomatous, and meningeal lymphocytosis. Abeta is consistently present in abundance in affected blood vessels but usually scanty within the parenchyma of the cerebral cortex. However, the cortex includes numerous activated microglia, occasionally in a plaque-like distribution and containing cytoplasmic Abeta. The cerebral white matter shows patchy gliosis and rarefaction, in some cases marked. Our findings (i) help to dissect one separate clinicopathological entity from what is likely to be a spectrum of primary angiitides of the CNS; (ii) have important therapeutic implications for one category of patients with amyloid-related vasculopathy; and (iii) may provide valuable insights into the development of amyloid-associated inflammation, of relevance not only to ABRA but also to Abeta-immunization-related encephalitis and to Alzheimer's disease.

摘要

中枢神经系统特发性或原发性血管炎(PACNS)和脑淀粉样血管病(CAA)是罕见的血管病变,通常被认为是不相关的疾病。然而,一些病例报告描述了散发性、与淀粉样β肽(Aβ)相关的CAA患者出现肉芽肿性血管炎。在此,我们描述了9例与Aβ相关血管炎(ABRA)患者的临床、神经放射学和神经病理学特征。将这些特征与文献中的个别病例报告相结合,使我们能够将ABRA定义为一种临床实体,并将其特征与PACNS的特征进行比较。ABRA的平均发病年龄(67岁)高于PACNS,但低于散发性非炎症性Aβ相关CAA。精神状态改变(59%)、头痛(35%)、癫痫发作和局灶性神经功能缺损(24%)较为常见。幻觉是12%病例的首发表现。大多数患者在MRI上有白质高信号,但这些信号与PACNS中的相似。脑脊液通常显示蛋白轻度升高和细胞增多。神经病理学显示血管破坏性炎症,通常为肉芽肿性,以及脑膜淋巴细胞增多。Aβ在受影响的血管中始终大量存在,但在大脑皮质实质内通常很少。然而,皮质包括大量活化的小胶质细胞,偶尔呈斑块样分布并含有细胞质Aβ。脑白质显示斑片状胶质增生和稀疏,在某些情况下较为明显。我们的发现(i)有助于从可能是中枢神经系统原发性血管炎谱中分离出一个单独的临床病理实体;(ii)对一类淀粉样血管病患者具有重要的治疗意义;(iii)可能为淀粉样蛋白相关炎症的发展提供有价值的见解,这不仅与ABRA有关,也与Aβ免疫接种相关脑炎和阿尔茨海默病有关。

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