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Reversible posterior leukoencephalopathy syndrome: A rare complication of hypertensive encephalopathy in children

机译:可逆性后脑白质脑病综合征:儿童高血压脑病的罕见并发症

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Abstract. Reversible posterior leukoencephalopathy syndrome is a recently defined cliniconeuroradiologic entity, rarely reportednin children. Hypertensive encephalopathy is the most common cause. A 4-year-old boy presented with reversible posteriornleukoencephalopathy syndrome manifested by headache, seizures, coma, papilledema and facial paralysis complicating severenarterial hypertension. Computed tomography scan of the brain showed bilateral low-density areas corresponding to the frontal,nparietooccipital white matter and to the internal capsula. Blood pressure was controlled within 4 days and clinical recoverynwas obtained within 5 days. Magnetic resonance imaging, performed 2 months later, was normal. The arterial hypertensionnwas caused by renal scars of bilateral vesico-renal reflux. The clinical course, pathophysiology and neuroimaging features ofnreversible posterior leukoencephalopathy syndrome in children are discussed.
机译:抽象。可逆性后脑白质脑病综合征是最近定义的临床神经放射学实体,很少在儿童中报道。高血压脑病是最常见的原因。一个4岁男孩表现出可逆性后脑白质脑病综合征,表现为头痛,癫痫发作,昏迷,乳头水肿和面神经麻痹,并伴有严重的高血压。电脑断层扫描显示大脑的双侧低密度区域与额叶,枕上枕叶白质和内囊相对应。在4天内控制血压,并在5天内获得临床恢复。 2个月后进行的磁共振成像正常。动脉高压是由双侧膀胱肾返流的肾脏瘢痕引起的。讨论了儿童不可逆性后脑白质脑病综合征的临床过程,病理生理和神经影像学特征。

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