Dementia lacking distinctive histologie features

作者：David S. Knopman, Angeline R. Mastri, William H. Frey, Jae Hoon Sung, T. D. Rustan · 发表于：Neurology · 年份：1990 · DOI：10.1212/wnl.40.2.251 · 被引用次数：378 · 研究领域：Alzheimer's disease research and treatments、Amino Acid Enzymes and Metabolism、Neurological and metabolic disorders

From a series of 460 dementia patients referred to a regional brain bank, 14 (3%) patients had a pathologic diagnosis of primary degeneration of the brain involving multiple sites (frontoparietal cortex, striatum, medial thalamus, substantia nigra, and hypoglossal nucleus), with cell loss and astrocytosis. There were no neuronal inclusions and essentially no senile plaques. This entity, which we have termed "dementia lacking distinctive histology" (DLDH), presented with memory loss and personality changes, and led to death, usually within 2 to 7 years. Dysarthria and dysphagia were prominent in the later phases of the illness in most patients. The psychometric findings of some of the patients were consistent with a "frontal" lobe dementia. A few patients had prominent caudate atrophy on CT as well as neuropathologically. Eight of our patients had positive family histories for neurologic disease, mainly dementia. DLDH, in addition to Pick's disease, is a major member of the frontal-lobe dementia group. In patients under age 70 years, the frontal lobe dementias represent an important diagnostic consideration.