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An autopsy case of Alzheimer's disease with amygdala-predominant Lewy pathology presenting with frontotemporal dementia-like psychiatric symptoms.
Beck, Goichi; Shigenobu, Kazue; Ukon, Koto; Yamashita, Rika; Yonenobu, Yuki; Morii, Eiichi; Hasegawa, Masato; Ikeda, Manabu; Murayama, Shigeo; Mochizuki, Hideki.
Afiliação
  • Beck G; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Shigenobu K; Department of Psychiatry, Asakayama General Hospital, Sakai, Japan.
  • Ukon K; Department of Pathology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Yamashita R; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Yonenobu Y; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Morii E; Department of Pathology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Hasegawa M; Dementia Research Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
  • Ikeda M; Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Japan.
  • Murayama S; Department of Neurology, Osaka University Graduate School of Medicine, Suita, Japan.
  • Mochizuki H; Brain Bank for Neurodevelopmental, Neurological and Psychiatric Disorders, Molecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University, Suita, Japan.
Neuropathology ; 42(2): 147-154, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35112739
ABSTRACT
Alzheimer's disease (AD) and frontotemporal dementia (FTD) are progressive neurodegenerative diseases associated with several cognitive and behavioral symptoms. It is sometimes difficult to distinguish AD from FTD in a patient because both of them can exhibit clinical overlap. In the present study, we report a case of a patient who showed sychiatric symptoms mimicking the behavioral variant of FTD (bvFTD) and combined AD amygdala-predominant Lewy pathologies on autopsy. The patient was a Japanese man who developed personality changes in his late 50s, presenting with obsessive-compulsive stereotypical behavior, stereotypy of speech, behavioral disinhibition, inertia, loss of empathy or sympathy, change in eating habits, and stimulus-bound behavior. He also frequently left during medical examinations. Eventually, he was clinically diagnosed as having possible bvFTD, according to the International Consensus Criteria for bvFTD. The patient died of systemic metastasis of gastric cancer at 69 years of age. Postmortem neuropathological examination revealed severe AD pathology (Braak Amyloid stage C, Consortium to Establish a Registry for Alzheimer's Disease [CERAD] stage C, Thal phase 5, and Braak AT8 stage IV) along with Lewy pathology and argyrophilic grains, predominantly in the amygdala. Furthermore, no transactivation response DNA-binding protein of 43 kDa (TDP-43) pathology was observed. Our results suggest that a combination of these pathologies causes bvFTD-like cognitive and behavioral symptoms. This case is very insightful when considering the lesions responsible for the psychiatric symptoms characteristic of bvFTD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Pick / Demência Frontotemporal / Doença de Alzheimer Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Pick / Demência Frontotemporal / Doença de Alzheimer Idioma: En Ano de publicação: 2022 Tipo de documento: Article