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可逆性后部白质脑病综合征的谱及潜在发病机制。

Spectrum and potential pathogenesis of reversible posterior leukoencephalopathy syndrome.

机构信息

Division of Neurology, Department of Medicine, Lehigh Valley Health Network, Allentown, Pennsylvania 18103, USA.

出版信息

J Stroke Cerebrovasc Dis. 2012 Nov;21(8):873-82. doi: 10.1016/j.jstrokecerebrovasdis.2011.05.010. Epub 2011 Jun 23.

Abstract

BACKGROUND

Controversy still exists over the etiology and pathophysiology of reversible posterior leukoencephalopathy syndrome (RPLS). This large single-center case series aims to describe the clinical and imaging features of RPLS in an attempt to deduce the etiology of the disorder and the mechanisms of brain injury.

METHODS

A retrospective chart and imaging review was conducted on 59 cases of RPLS in 55 patients.

RESULTS

Five RPLS imaging patterns were observed: posterior predominant (n = 40), anterior predominant (n = 7), diffuse lesion (n = 7), basal ganglia predominant (n = 3), and brainstem/cerebellum predominant patterns (n = 2). RPLS resulted in permanent neurologic deficits in 14 patients and death in 4 patients. Hypertension was seen in 57 (97%) cases, and mean arterial blood pressure exceeded 140 mm Hg in 30 (51%) cases. Follow-up magnetic resonance imaging scans revealed a significant worsening of vasogenic edema in 2 cases, both with persistent hypertension. Magnetic resonance imaging scans revealed areas of ischemia in 14 cases, all within or at areas closely adjacent to vasogenic edema. Diffuse vasculopathy was seen in 8 cases. There was a lack of correlation between the presence of vasculopathy and the degree of vasogenic edema (P = .62), but a correlation was suggested between ischemia and vasculopathy (P = .02).

CONCLUSIONS

This study strongly suggests that hypertension-induced vasodilation rather than vasoconstriction-mediated hypoxia is likely the major mechanism responsible for the development of vasogenic edema, and that vasoconstriction may contribute to the development of ischemia in RPLS.

摘要

背景

可逆性后部脑白质病综合征(RPLS)的病因和病理生理学仍存在争议。本大型单中心病例系列旨在描述 RPLS 的临床和影像学特征,试图推断该疾病的病因和脑损伤机制。

方法

对 55 例患者的 59 例 RPLS 进行回顾性图表和影像学回顾。

结果

观察到 5 种 RPLS 影像学模式:后部为主(n = 40)、前部为主(n = 7)、弥漫性病变(n = 7)、基底节为主(n = 3)和脑干/小脑为主模式(n = 2)。RPLS 导致 14 例患者永久性神经功能缺损和 4 例死亡。57 例(97%)存在高血压,30 例(51%)平均动脉压超过 140mmHg。随访磁共振成像扫描显示 2 例血管源性水肿明显恶化,均持续存在高血压。14 例磁共振成像扫描显示存在缺血区,均位于或紧邻血管源性水肿区域内或附近。8 例存在弥漫性血管病。血管病的存在与血管源性水肿的程度之间无相关性(P =.62),但缺血与血管病之间存在相关性(P =.02)。

结论

本研究强烈表明,高血压引起的血管扩张而非血管收缩介导的缺氧可能是导致血管源性水肿发展的主要机制,而血管收缩可能导致 RPLS 中的缺血发生。

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