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Japanese

Two autopsy cases of Creutzfeldt-Jakob disease Jun KINOSHITA 1 , Ryoichi MIZUNO 1 , Saburo YAGISHITA 2 , Manichi IIDA 3 , Michihiko MATSUSHITA 4 , Toshiki USHIAMA 5 1Dept. of Neurology and Psychiatry, Yokohama City Univ. School of Med. 2Second Dept. of Pathology, Yokohama City Univ. School of Med. 3First Dept. of Pathology, Yokohama City Univ. School of Med. 4Dept. of Neurosurgery, Yokohama Red-Cross Hospital 5Second Dept. of Internal Medicine, Yokohama Minami-Kyosai Hospital pp.452-459
Published Date 1972/6/10
DOI https://doi.org/10.11477/mf.1431903399
  • Abstract
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Clinical and histopathological findings of two cases of Creutzfeldt-Jakob disease were presented.

1) The first case, a 41 year-old male, showed initial signs of aphasia, amnesia and visual dis-turbances (cortical blindness). Organic dementia developed stepwise together with febrile episodes under delirious state accompained with clonic focal seizures and myoclonic jerks of the upper half of the body and muscular atrophy of the lower limbs. Electroencephalographically "periodic synchronous discharge" was noticed. Death occurr-ed under akinetic mutism with quadriparesis in flexion, 14 months after the onset of symptoms.


Copyright © 1972, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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