Ozgencil E, Gülücü C, Yalçýn S, Alanoğlu Z, Unal N, Oral M, Tulunay M
Ankara University Medical Faculty, Department of Anaesthesiology and ICU, Ibn-i Sina Hospital, Sihhiye, 06100 Ankara, Turkey.
Neth J Med. 2007 Jul-Aug;65(7):274.
Posterior reversible encephalopathy syndrome (PRES) is a rare neurological condition identifiable by clinical presentation and MRI appearance.1 Patients present with headache, seizures, loss of vision and altered mental function. The pathogenesis of the syndrome is poorly understood. One hypothesis is that cerebral vasospasm results in cerebral ischaemia and subsequent development of T2 hyperintensity, and the other is a temporary failure of the autoregulatory capabilities of the cerebral vessels, leading to hyperperfusion, breakdown of the blood-brain barrier, and consequent vasogenic oedema. It is believed that a rapid rise in blood pressure overcomes cerebral autoregulatory mechanisms with abrupt dilatation of cerebral arterioles. We report a patient with systemic lupus erythematosus and PRES after recurrent spontaneous abortion.
后部可逆性脑病综合征(PRES)是一种罕见的神经系统疾病,可通过临床表现和磁共振成像(MRI)表现来识别。患者表现为头痛、癫痫发作、视力丧失和精神功能改变。该综合征的发病机制尚不清楚。一种假说是脑血管痉挛导致脑缺血及随后T2高信号的出现,另一种假说是脑血管自动调节功能暂时失效,导致脑血流灌注过多、血脑屏障破坏,进而引起血管源性水肿。据信血压的快速升高会突破脑自动调节机制,导致脑小动脉突然扩张。我们报告一例系统性红斑狼疮患者在反复自然流产后发生后部可逆性脑病综合征。