Abstract
In 1894, the term “encephalitis subcorticalis chronica progressiva” was introduced by Otto Binswanger to refer to a noninflammatory disease of the cerebral white matter. It was detected in eight patients who presented a slow progression of mental deterioration, which he attributed to reduced cerebral blood flow resulting from arteriosclerosis [4] Until recently Binswanger’s disease or subcortical arteriosclerotic encephalopathy (SAE) was considered to be a rare disease, but in recent years, thanks to modern neuroimaging techniques such as cranial computed tomography (CCT) [13,29,30,32,33] and magnetic resonance imaging (MRI) [5,10,14,34], this disorder has been detected with greater frequency. The typical clinical picture includes a constellation of insidiously progressive deterioration of memory, mood, and cognition; focal neurological signs and symptoms with bilateral pyramidal tract signs; less often, pseudobulbar palsy; and finally, gait and sphincter disturbances [12,23,24].
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© 1991 Springer-Verlag Berlin Heidelberg
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Broich, K., Hartmann, A., Solymosi, L., Naaz, B., Dettmers, C., Fric, M. (1991). Regional Cerebral Blood Flow in Binswanger’s Disease. In: Hartmann, A., Kuschinsky, W., Hoyer, S. (eds) Cerebral Ischemia and Dementia. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76208-6_34
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DOI: https://doi.org/10.1007/978-3-642-76208-6_34
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