Prior to any evaluation cf morphologic brain change, a decision must be made whether a given alteration is associated with aging or with disease. Patients with disease-related lesions may be in a clinically silent phase of a disease or show overt symptoms. Neurofibrillary tangles and neuropil threads are the hallmarks of Alzheimer's disease. They should nor be considered to be age-related changes, even when they are present only in small numbers. In general, the initial changes consist of neurofibrillary tangles and neuropil threads. Plaques (amyloid deposits and/or neuritic plaques) are consistently present in the end stage of the disease. Initial neurofibrillary tangles and neuropil threads develop at specific cortical predilection sites. The changes;hen spread in a predictable. nonrandom manner across other portions of the telencephalic cortex. The sequential changes in the distribution pattern of the lesions provide the basis for a staging procedure that takes the slow and gradual progression of the destructive process into consideration. The staging procedure provides accurate diagnoses in the initial stages and even reveals blain changes developing prior to the appearance of clinical symptoms. It is thus advantageous in characterizing nondemented controls. The staging procedure can be carried out easily and does not require knowledge of clinical data, quantitative assessments, or adjustments for the age of the patients. Application of advanced silver techniques (Gallyas, Campbell-Switzer) to demonstrate Alzheimer's disease-related lesions also allows recognition of the hallmarks of other disorders, such as Lewy body disease (Parkinson's disease) and dementia with argyrophilic grains, which frequently co-occur with Alzheimer's disease.
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Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Arnold, Steven E.
Hyman, Bradley T.
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Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Hyman, Bradley T.
Flory, Jill
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Univ Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Flory, Jill
Damasio, Antonio R.
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Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Damasio, Antonio R.
Van Hoesen, Gary W.
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Univ Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
机构:
Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Arnold, Steven E.
Hyman, Bradley T.
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Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Hyman, Bradley T.
Flory, Jill
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Univ Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Flory, Jill
Damasio, Antonio R.
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Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Damasio, Antonio R.
Van Hoesen, Gary W.
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Univ Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA
Univ Iowa, Dept Neurol, Coll Med, Iowa City, IA 52242 USAUniv Iowa, Dept Anat, Coll Med, Iowa City, IA 52242 USA