| Item type |
[ELS]紀要論文 / Departmental Bulletin Paper(1) |
| 公開日 |
2019-03-27 |
| タイトル |
|
|
タイトル |
Probable and "definitive" diagnosis of a formidable disease : Creutzfeldt-Jacob disease |
|
言語 |
en |
| 言語 |
|
|
言語 |
eng |
| キーワード |
|
|
主題 |
CJD, differential diagnosis |
| 資源タイプ |
|
|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
departmental bulletin paper |
| 著者 |
Takagaki, Masao
Sumioka, Mayumi
Kazui, Hiroaki
|
| 抄録(英) |
|
|
内容記述タイプ |
Abstract |
|
内容記述 |
A 75-year-old female with rapidly progressive dementia, pyramidal and extrapyramidal signs, myoclonus, and mutism received a diagnosis of probable sporadic Creutzfeldt-Jakob disease (sCJD) after eliminating other possible candidates, such as normal pressure hydrocephalus (NPH), some form of encephalopathy, and so on. However, postmortem brain biopsy revealed the case to be non-CJD. Facing the triad of progressive dementia, myoclonus, and pyramidal/extrapyramidal features, Alzheimer's disease (AD) should be retrospectively considered if the disease course is long and dementia with Lewy bodies (DLB) is the differential diagnosis if Parkinsonism is present. Findings on electroencephalogram (EEG) or in cerebrospinal fluid (CSF) typical of CJD do not exclude AD or DLB. |
|
言語 |
en |
| 書誌情報 |
en : AINO JOURNAL
巻 6,
号 1,
p. 75-78,
ページ数 4,
発行日 2008-03-31
|
| ISSN |
|
|
収録物識別子タイプ |
PISSN |
|
収録物識別子 |
1348480X |
KJ00005223113.pdf (672.0 kB)
