原发性进行性失语症。

A Kertesz, D G Munoz
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引用次数: 0

摘要

原发性进行性失语是一种重要的临床综合征,是匹克病和匹克复杂病理的常见早期表现。临床定义为缓慢进行性语言障碍,与其他认知或行为缺陷相对隔离至少2年。随后,它可能与类似额叶痴呆(FLD)的行为改变、锥体外系表现和类似皮质基底变性(CBD)的失用症以及运动神经元疾病相关。常见的导致缄默症的不流利或词性变异(额叶受罚)和流利或语义变异(颞叶受罚)都是公认的。CT、MRI和SPECT的神经影像学检查是确认诊断的有用辅助手段。PPA是额颞叶变性或Pick复合体的一种表现,这可能是仅次于AD的第二常见的退行性痴呆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary progressive aphasia.

Primary progressive aphasia is an important recently emphasized clinical syndrome that is a common early manifestation of Pick's disease and Pick complex pathology. It is defined clinically as slowly progressive language disturbance that remains relatively isolated from other cognitive or behavioral deficits for at least 2 years. Subsequently, it may become associated with behavioral changes similar to those in frontal lobe dementia (FLD), extrapyramidal manifestations, and apraxia similar to corticobasal degeneration (CBD) and with motor neuron disease. Both the common nonfluent or logopenic variety leading to mutism (frontal involvement) and fluent or semantic varieties (temporal involvement) are recognized. Neuroimaging with CT, MRI, and SPECT are useful adjuncts confirming the diagnosis. PPA is a manifestation of frontotemporal degeneration or Pick complex, which is probably the second most common degenerative dementia after AD.

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