NEURONAL ULTRASTRUCTURAL ABNORMALITIES IN A PATIENT WITH FRONTOTEMPORAL DEMENTIA AND MOTOR-NEURON DISEASE

被引:22
作者
CHANG, L
CORNFORD, M
MILLER, BL
ITABASHI, H
MENA, I
机构
[1] UNIV CALIF LOS ANGELES,HARBOR MED CTR,DEPT PATHOL,DIV NUCL MED,TORRANCE,CA 90509
[2] UNIV CALIF LOS ANGELES,HARBOR MED CTR,DEPT RADIOL,DIV NUCL MED,TORRANCE,CA 90509
来源
DEMENTIA | 1995年 / 6卷 / 01期
关键词
FRONTOTEMPORAL DEMENTIA; MOTOR NEURON DISEASE; NEURONAL INCLUSIONS; MITOCHONDRIA; ULTRASTRUCTURE;
D O I
10.1159/000106915
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Motor neuron disease (MND) can be associated with frontotemporal dementia (FTD) and circumscribed lobar atrophy of frontal and temporal lobes. Neuropathological correlations were sought in the post mortem studies from a woman with these associated conditions. Cerebral blood flow imaging and autopsy showed cortical abnormalities in the frontal and temporal lobes, but typical argyrophilic Pick's bodies were absent and ubiquitin-positive neuronal cytoplasmic inclusions were rare. However, hematoxylin and eosin staining revealed eosinophilic, granular, central cytoplasmic 'clearing' in most neurons of the substantia nigra and in cervical anterior horn cells. Electron microscopy showed that these neurons contained a central cytoplasmic zone cleared of neuromelanin and normal cytoplasmic organelles containing small mitochondria with matrix inclusions and randomly oriented filamentous material. A mitochondrial dysfunction or defective transport of mitochondria into axonal processes needs to be studied as a potential cause for the coassociation of MND and FTD.
引用
收藏
页码:1 / 8
页数:8
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