Pathologic diagnosis of non-Alzheimer type dementia.
- Author:
Ming-wei ZHU
1
;
Lu-ning WANG
;
Xiang-hong LI
;
Ya-zhuo HU
Author Information
- Publication Type:Journal Article
- MeSH: Aged; Aged, 80 and over; Brain; pathology; Dementia; pathology; Diagnosis, Differential; Female; Humans; Lewy Body Disease; pathology; Male; Neurodegenerative Diseases; pathology; Neurons; pathology; Parkinson Disease; pathology; Pick Disease of the Brain; pathology; Supranuclear Palsy, Progressive; pathology
- From: Chinese Journal of Pathology 2004;33(5):408-412
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo characterize histopathologic features of non-Alzheimer type dementia.
METHODSBodian, Gallyas-Braak silver staining, tau and ubiquitin immunohistochemistry were applied in an analysis of 22 cases of autopsy-proven neurodegenerative dementia. Appearance, distribution and immunoreactivity of neuronal and glial inclusions in the brain were observed. The final histological diagnoses were made according to the pathological criteria for several types of common non-Alzheimer type dementia.
RESULTSAmong the 22 cases of neurodegenerative dementia, 12 cases were identified as non-Alzheimer type dementia, including Pick's disease (2 cases), progressive supranuclear palsy (3 cases) and corticobasal degeneration (3 cases), dementia with Lewy bodies (1 case), and Parkinson's disease (3 cases). Another 10 cases consisted of pure Alzheimer's disease (AD, 9 cases) and AD combined with argyrophilic grain disease (1 case). Characteristic neuronal and glial inclusions, such as classical and cortical Lewy body, Pick body, Globous NFTs, astrocytic plaque and tufted astrocyte, argyrophilic grain were found in the brains of non-Alzheimer type dementia. Classical and cortical Lewy bodies were not argyrophilic but were immunoreactive to ubiquitin. Pick bodies, Globous NFTs, astrocytic plaques, tufted astrocytes and argyrophilic grains were all argyrophilic. Pick bodies showed tau and ubiquitin immunoreactivity. However, Globous NFTs, astrocytic plaques, tufted astrocytes, and argyrophilic grains were reactive only to tau immunohistochemistry.
CONCLUSIONSFindings of characteristic neuronal and glial inclusions may help to differentiate non-Alzheimer type dementia from AD, and in conjunction with Gallyas-Braak staining and immunohistochemistry for tau and ubiquitin, to further define histopathologic subcategories of non-Alzheimer type dementia.