An Autopsy Case of Pick's Disease.
- Author:
Kwang Soo LEE
1
;
Dong Suk SHIM
;
Seong Min PARK
;
Yeon Soo LEE
;
Ki Hwa YANG
Author Information
1. Department of Neurology, The Catholic University of Korea.
- Publication Type:Case Report
- Keywords:
Pick's disease;
Fronto-temporal dementia;
Autopsy
- MeSH:
Atrophy;
Autopsy*;
Brain;
Cerebrum;
Compulsive Behavior;
Dementia;
Dilatation;
Encephalomalacia;
Humans;
Lateral Ventricles;
Male;
Memory;
Middle Aged;
Neurodegenerative Diseases;
Neurons;
Pick Disease of the Brain*;
Pneumonia, Aspiration;
Pyramidal Cells;
Sepsis;
Temporal Lobe
- From:Journal of the Korean Neurological Association
2000;18(6):786-789
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Pick's disease is a rare neurodegenerative disorder presenting cortical type of dementia. Pick's disease shows unique clinical and pathological features, that are due to a degeneration of fronto-temporal lobes of the cerebrum. The authors experienced a case of Pick's disease in a 58-year-old male patient who had dementia symptoms for five years. The patient showed compulsive behavior since five years ago. Memory decline started from four years ago and progressed. Brain CT disclosed lobar atrophy of the cerebral gyri in frontal and temporal lobes. He died of septicemia associated with aspiration pneumonia. At autopsy, both cerebral hemispheres showed marked encephalomalacia. The gyral atrophy was moderately severe in prefrontal and anterior temporal lobes. Coronal section disclosed moderate dilatation of the lateral ventricles. Microscopically, there were marked neuronal loss in prefrontal and anterior temporal cortices. Also noted were Pick's cells and Pick's body in occasional pyramidal cells preserved.
