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Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice
INTRODUCTION: Creutzfeldt–Jakob disease (CJD) is an important dementia disorder. However, clinical diagnosis can be difficult and delayed for many primary physicians caring for dementia patients. The aim of the present study was to describe clinical and neuropathological results of an individual wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japan Medical Association
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889787/ https://www.ncbi.nlm.nih.gov/pubmed/33615025 http://dx.doi.org/10.31662/jmaj.2018-0060 |
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author | Tanaka, Yukiko Ikeda, Masaki Mihara, Ban Ikeda, Yoshio Sato, Katsuya Kitamoto, Tetsuyuki Takao, Masaki |
author_facet | Tanaka, Yukiko Ikeda, Masaki Mihara, Ban Ikeda, Yoshio Sato, Katsuya Kitamoto, Tetsuyuki Takao, Masaki |
author_sort | Tanaka, Yukiko |
collection | PubMed |
description | INTRODUCTION: Creutzfeldt–Jakob disease (CJD) is an important dementia disorder. However, clinical diagnosis can be difficult and delayed for many primary physicians caring for dementia patients. The aim of the present study was to describe clinical and neuropathological results of an individual with CJD who was seen by a community hospital. Our report may inform many primary physicians on understanding the significance of CJD. METHODS: Clinical information was obtained from medical records. Neuropathological and biochemical analyses were performed using autopsied brain. RESULTS: A 58-year-old Japanese man who had worked as a carpenter developed memory and executive function impairments. He was initially diagnosed as having Alzheimer’s disease based on clinical and neuroradiological analyses. Myoclonus was observed in the later stage of clinical course. Hyperintense lesions on diffusion-weighted images were observed in the cerebral cortex in later stage. Analysis of cerebrospinal fluid showed increased levels of total tau and phospho-tau protein. However, 14-3-3 protein and amyloid β (1–42) were normal. Genetic analysis of the PRNP gene showed methionine homozygosity at codon 129 and glutamate homozygosity at codon 219. The results of neuropathological analysis were consistent with sporadic CJD (MM2 cortical type with some type 1 pattern of 3F4 immunoreactivity). Western blot analysis of the frontal and cerebellar cortex revealed a type 2 and type 1 pattern of proteinase K (PK)-resistant prion protein, respectively. No Alzheimer’s pathology was present. CONCLUSIONS: Our experience may help primary physicians to assess dementia patients. Since atypical forms of prion disease are now well-established, we need to consider prion disease in dementia patients. Clinical examination alone is not enough for dementia workup; thus, we must understand the importance of neuropathological study and encourage autopsy to reach a definite diagnosis of dementia. |
format | Online Article Text |
id | pubmed-7889787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Japan Medical Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-78897872021-02-19 Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice Tanaka, Yukiko Ikeda, Masaki Mihara, Ban Ikeda, Yoshio Sato, Katsuya Kitamoto, Tetsuyuki Takao, Masaki JMA J Original Research Article INTRODUCTION: Creutzfeldt–Jakob disease (CJD) is an important dementia disorder. However, clinical diagnosis can be difficult and delayed for many primary physicians caring for dementia patients. The aim of the present study was to describe clinical and neuropathological results of an individual with CJD who was seen by a community hospital. Our report may inform many primary physicians on understanding the significance of CJD. METHODS: Clinical information was obtained from medical records. Neuropathological and biochemical analyses were performed using autopsied brain. RESULTS: A 58-year-old Japanese man who had worked as a carpenter developed memory and executive function impairments. He was initially diagnosed as having Alzheimer’s disease based on clinical and neuroradiological analyses. Myoclonus was observed in the later stage of clinical course. Hyperintense lesions on diffusion-weighted images were observed in the cerebral cortex in later stage. Analysis of cerebrospinal fluid showed increased levels of total tau and phospho-tau protein. However, 14-3-3 protein and amyloid β (1–42) were normal. Genetic analysis of the PRNP gene showed methionine homozygosity at codon 129 and glutamate homozygosity at codon 219. The results of neuropathological analysis were consistent with sporadic CJD (MM2 cortical type with some type 1 pattern of 3F4 immunoreactivity). Western blot analysis of the frontal and cerebellar cortex revealed a type 2 and type 1 pattern of proteinase K (PK)-resistant prion protein, respectively. No Alzheimer’s pathology was present. CONCLUSIONS: Our experience may help primary physicians to assess dementia patients. Since atypical forms of prion disease are now well-established, we need to consider prion disease in dementia patients. Clinical examination alone is not enough for dementia workup; thus, we must understand the importance of neuropathological study and encourage autopsy to reach a definite diagnosis of dementia. Japan Medical Association 2019-06-06 2019-09-04 /pmc/articles/PMC7889787/ /pubmed/33615025 http://dx.doi.org/10.31662/jmaj.2018-0060 Text en Copyright © Japan Medical Association http://creativecommons.org/licenses/by/4.0/ JMA Journal is an Open Access journal distributed under the Creative Commons Attribution 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Research Article Tanaka, Yukiko Ikeda, Masaki Mihara, Ban Ikeda, Yoshio Sato, Katsuya Kitamoto, Tetsuyuki Takao, Masaki Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title | Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title_full | Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title_fullStr | Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title_full_unstemmed | Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title_short | Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice |
title_sort | importance of neuropathological diagnosis of dementia patients in family practice |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889787/ https://www.ncbi.nlm.nih.gov/pubmed/33615025 http://dx.doi.org/10.31662/jmaj.2018-0060 |
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