Del Bigio Marc R
Department of Pathology, University of Manitoba, and Manitoba Institute for Child Health, Winnipeg, Canada.
Brain Pathol. 2004 Jul;14(3):317-24. doi: 10.1111/j.1750-3639.2004.tb00071.x.
The literature concerning brain damage due to hydrocephalus, especially in children and animal models, is reviewed. The following conclusions are reached: 1. Hydrocephalus has a deleterious effect on brain that is dependent on magnitude and duration of ventriculomegaly and modified by the age of onset. 2. Animal models have many histopathological similarities to humans and can be used to understand the pathogenesis of brain damage. 3. Periventricular axons and myelin are the primary targets of injury. The pathogenesis has similarities to traumatic and ischemic white matter injury. Secondary changes in neurons reflect compensation to the stress or ultimately the disconnection. 4. Altered efflux of extracellular fluid could result in accumulation of waste products that might interfere with neuron function. Further research is needed in this as well as the blood-brain barrier in hydrocephalus. 5. Some, but not all, of the changes are preventable by shunting CSF. However, axon loss cannot be reversed, therefore shunting in a given case must be considered carefully. 6. Experimental work has so far failed to show any benefit in reducing CSF production. Pharmacologic protection of the brain, at least as a temporary measure, holds some promise but more pre-clinical research is required.
本文综述了有关脑积水导致脑损伤的文献,特别是在儿童和动物模型方面的研究。得出以下结论:1. 脑积水对大脑有有害影响,这种影响取决于脑室扩大的程度和持续时间,并受发病年龄的影响。2. 动物模型在组织病理学上与人类有许多相似之处,可用于了解脑损伤的发病机制。3. 脑室周围的轴突和髓鞘是主要的损伤靶点。其发病机制与创伤性和缺血性白质损伤相似。神经元的继发性变化反映了对压力的代偿或最终的连接中断。4. 细胞外液流出的改变可能导致废物积累,进而可能干扰神经元功能。在这方面以及脑积水的血脑屏障方面都需要进一步研究。5. 部分(但并非全部)变化可通过脑脊液分流预防。然而,轴突损失无法逆转,因此在特定病例中进行分流必须谨慎考虑。6. 迄今为止,实验工作未能显示出减少脑脊液生成有任何益处。对大脑的药物保护,至少作为一种临时措施,有一定前景,但需要更多的临床前研究。