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Primary angiitis of the central nervous system: emerging variants

机译:中枢神经系统原发性血管炎:新出现的变异

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Background: Primary angiitis of the central nervous system (PACNS), a serious disease, has not featured prominently in the spectrum of multi-organ disease seen in vasculitis clinics. Aim: To evaluate the presentation, natural history and features of PACNS variants and compare to those of systemic vasculitides. Design: Retrospective analysis. Methods: Patients (n= 105) presented during 1988-2003 to a tertiary regional vasculitis clinic receiving unselected disease types. Data were collected from a clinical database, patient and laboratory records. Results: The frequency of PACNS presentation rose over the study period, compared with most of the other vasculitides. When PACNS was divided into small- and middle-sized vessel disease (SVD/MVD), their clinical courses differed substantially. SVD PACNS was responsive to immunosuppressive drugs, but relapsed during prolonged periods in all patients on maintenance immunosuppressives, or after withdrawal of treatment, causing recurrent, severe and irreversible CNS injury. MVD PACNS had isolated episodes at presentation, with a paucity of relapses during prolonged follow-up. Discussion: Similarities between SVD PACNS and microscopic polyarteritis suggest the former may represent a limited form of the latter. MVD PACNS has a distinctly more benign relapse pattern than its multisystem counterpart polyarteritis nodosa. Acute-phase serology was useful in designating inflammatory processes at presentation of patients presenting with encephalopathy caused by SVD only, but were unhelpful in defining relapses in this form of PACNS, the definition of which in all cases rested on clinical assessment and MR scanning. Direct cerebral angiography was not diagnostic in any case of SVD PACNS; positive brain biopsy is diagnostically unequivocal, but the total clinical syndrome with imaging may establish a diagnosis with highest probability. In MVD PACNS, angiography with MR scan proved diagnostic. We suggest an algorithm for a rational, minimally invasive approach to investigation. In PACNS, SVD and MVD are important variants, and decisions about therapy should incorporate these distinctions.
机译:背景:中枢神经系统原发性血管炎(PACNS)是一种严重的疾病,在血管炎诊所所见的多器官疾病谱图中并未突出显示。目的:评估PACNS变体的表现,自然历史和特征,并与全身性血管炎进行比较。设计:回顾性分析。方法:1988-2003年间就诊于三级区域性血管炎诊所的患者(n = 105)接受了未选择的疾病类型。从临床数据库,患者和实验室记录中收集数据。结果:与大多数其他血管肽相比,在研究期间PACNS出现的频率增加。当PACNS分为中小血管疾病(SVD / MVD)时,它们的临床过程有很大不同。 SVD PACNS对免疫抑制药有反应,但在所有维持免疫抑制药的患者中或在停药后长时间内均会复发,从而导致复发,严重和不可逆转的CNS损伤。 MVD PACNS出现时表现为孤立性发作,长期随访期间复发很少。讨论:SVD PACNS与微观多发性动脉炎之间的相似性表明前者可能代表后者的有限形式。 MVD PACNS比其多系统结节性多发性多发性结节性关节炎具有明显更良性的复发模式。急性期血清学仅可用于在出现由SVD引起的脑病的患者时指定炎症过程,但对于定义这种形式的PACNS的复发无济于事,在所有情况下其定义均取决于临床评估和MR扫描。在任何情况下,SVD PACNS均不能直接诊断脑血管造影。阳性的脑活检在诊断上是明确的,但是具有影像学的总临床综合征可能会以最高的概率建立诊断。在MVD PACNS中,经MR扫描的血管造影证明具有诊断意义。我们建议一种用于合理,微创方法进行调查的算法。在PACNS中,SVD和MVD是重要的变体,有关治疗的决定应纳入这些区别。

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