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后可逆性脑病综合征的神经影像学表现

Neuroimaging in posterior reversible encephalopathy syndrome.

作者信息

Lamy C, Oppenheim C, Méder J F, Mas J L

机构信息

Neurology Department, Hôpital Sainte-Anne, 1, rue Cabanis, 75674 Paris, France.

出版信息

J Neuroimaging. 2004 Apr;14(2):89-96.

Abstract

The terms posterior reversible leukoencephalopathy, reversible posterior cerebral edema syndrome, and posterior reversible encephalopathy syndrome (PRES) all refer to a clinicoradiologic entity characterized by headaches, confusion, visual disturbances, seizures, and posterior transient changes on neuroimaging. Clinical findings are not sufficiently specific to readily establish the diagnosis; in contrast, magnetic resonance imaging pattern is often characteristic and represents an essential component of the diagnosis of PRES. Typical lesions predominate in the posterior white matter, with some involvement of the overlying cortex; are hyperintense on T2-weighted images; and are usually hypointense or isointense on diffusion-weighted images, with an increase of the apparent diffusion coefficient, indicating vasogenic edema. The pathogenesis is incompletely understood, although it seems to be related to the breakthrough of autoregulation and endothelial dysfunction. Since its initial description, this syndrome has been subsequently described in an increasing number of medical conditions, including hypertensive encephalopathy, eclampsia, and the use of cytotoxic and immunosuppressive drugs. The diagnosis has important therapeutic and prognostic implications because the reversibility of the clinical and radiologic abnormalities is contingent on the prompt control of blood pressure and/or discontinuing the offending drug. On the contrary, when unrecognized, conversion to irreversible cytotoxic edema may occur.

摘要

术语“后部可逆性白质脑病”“可逆性后脑水肿综合征”以及“后部可逆性脑病综合征(PRES)”均指一种临床影像学实体,其特征为头痛、意识模糊、视觉障碍、癫痫发作以及神经影像学上的后部短暂性改变。临床发现并不具有足够的特异性来轻易确诊;相比之下,磁共振成像模式通常具有特征性,是PRES诊断的重要组成部分。典型病变主要位于后部白质,部分累及上方皮质;在T2加权图像上呈高信号;在扩散加权图像上通常呈低信号或等信号,表观扩散系数增加,提示血管源性水肿。尽管其发病机制似乎与自动调节功能障碍和内皮功能障碍有关,但尚未完全明确。自首次描述以来,该综合征在越来越多的医学病症中被报道,包括高血压脑病、子痫以及使用细胞毒性和免疫抑制药物。该诊断具有重要的治疗和预后意义,因为临床和影像学异常的可逆性取决于血压的迅速控制和/或停用致病药物。相反,如果未被识别,可能会转变为不可逆的细胞毒性水肿。

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