Memory and Aging Center, University of California, San Francisco, CA 94143-1207, USA.
Behav Neurol. 2013;26(1-2):95-106. doi: 10.3233/BEN-2012-120255.
The role of biomarkers in predicting pathological findings in the frontotemporal dementia (FTD) clinical spectrum disorders is still being explored. We present comprehensive, prospective longitudinal data for a 66 year old, right-handed female who met current criteria for the nonfluent/agrammatic variant of primary progressive aphasia (nfvPPA). She first presented with a 3-year history of progressive speech and language impairment mainly characterized by severe apraxia of speech. Neuropsychological and general motor functions remained relatively spared throughout the clinical course. Voxel-based morphometry (VBM) showed selective cortical atrophy of the left posterior inferior frontal gyrus (IFG) and underlying insula that worsened over time, extending along the left premotor strip. Five years after her first evaluation, she developed mild memory impairment and underwent PET-FDG and PiB scans that showed left frontal hypometabolism and cortical amyloidosis. Three years later (11 years from first symptom), post-mortem histopathological evaluation revealed Pick's disease, with severe degeneration of left IFG, mid-insula, and precentral gyrus. Alzheimer's disease (AD) (CERAD frequent/Braak Stage V) was also detected. This patient demonstrates that biomarkers indicating brain amyloidosis should not be considered conclusive evidence that AD pathology accounts for a typical FTD clinical/anatomical syndrome.
生物标志物在预测额颞叶痴呆(FTD)临床谱系障碍的病理发现中的作用仍在探索中。我们提供了一位 66 岁、右利手女性的全面、前瞻性纵向数据,她符合原发性进行性失语症(nfvPPA)的非流利/语法障碍变异的当前标准。她首次出现了 3 年的进行性言语和语言障碍病史,主要表现为严重的言语失用症。神经心理学和一般运动功能在整个临床过程中相对保留。基于体素的形态测量学(VBM)显示左后下额回(IFG)和下脑岛的选择性皮质萎缩,随着时间的推移逐渐加重,沿左运动前区延伸。首次评估 5 年后,她出现轻度记忆障碍,并接受了 PET-FDG 和 PiB 扫描,显示左额叶代谢减退和皮质淀粉样变性。3 年后(首次症状出现 11 年后),尸检组织病理学评估显示 Pick 病,左 IFG、中脑岛和中央前回严重退化。还检测到阿尔茨海默病(AD)(CERAD 频繁/Braak 第 V 期)。该患者表明,提示脑淀粉样蛋白的生物标志物不应被视为 AD 病理学导致典型 FTD 临床/解剖综合征的确凿证据。