Taylor Kirsten I, Probst Alphonse, Miserez André R, Monsch Andreas U, Tolnay Markus
Marie Curie Fellow at the University of Cambridge, Cambridge, UK.
Nat Clin Pract Neurol. 2008 Apr;4(4):226-32. doi: 10.1038/ncpneuro0746. Epub 2008 Feb 19.
Background A 66-year-old man presented with a 3-year history of personality changes marked by increasing apathy, social withdrawal and deficits in complex attention, and a 1-year history of progressive memory problems and difficulties in planning and carrying out complex tasks. Investigations Three neuropsychological examinations over 2 years, neurological examination, routine laboratory tests, brain MRI, single-photon emission CT scan, genetic analyses, and neuropathological examination. Diagnosis A clinical diagnosis of frontal-variant frontotemporal dementia was superseded by postmortem neuropathological evidence, which established a diagnosis of frontal-variant Alzheimer's disease. Management The patient and his spouse were referred for counseling, and the patient was referred for follow-up examinations.
一名66岁男性,有3年人格改变病史,表现为日益淡漠、社交退缩及复杂注意力缺陷,还有1年进行性记忆问题及计划和执行复杂任务困难的病史。
2年内进行了三次神经心理学检查、神经系统检查、常规实验室检查、脑部MRI、单光子发射CT扫描、基因分析及神经病理学检查。
临床诊断为额颞叶痴呆额部变异型,尸检神经病理学证据将其推翻,确诊为额颞叶痴呆额部变异型阿尔茨海默病。
患者及其配偶被转介接受咨询,患者被转介接受随访检查。