一个难以捉摸的诊断——后皮质萎缩

A. Filatov
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引用次数: 0

摘要

后皮质萎缩(PCA)是一种神经退行性综合征,其特征为进行性失用症、阅读障碍,最显著的是视觉知觉和视觉空间能力的丧失。在大多数情况下,枕叶、顶叶和颞叶后皮层的神经退行性变是阿尔茨海默病视觉变型(AD)的结果。较不常见的病因包括皮质基底变性、路易体痴呆(DLB)和朊病毒病的Heidenhain变体。目前尚不清楚是什么导致这些情况出现PCA。鉴于其罕见和多变的表现,误诊是常见的。我们提出一个60岁的妇女与PCA谁是最初未确诊的情况下。她对多奈哌齐和美金刚的治疗明显改善,提示AD可能是其发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Elusive Diagnosis - Posterior Cortical Atrophy
Posterior Cortical Atrophy (PCA) is a neurodegenerative syndrome characterized by progressive apraxia, dyslexia and most strikingly, loss of visual perceptual and visuospatial ability. In most cases, neuro-degeneration of the occipital, parietal, and posterior temporal cortices occurs as a consequence of the Visual Variant of Alzheimer disease (AD). Less frequent etiologies include Corticobasal Degeneration, Dementia with Lewy bodies (DLB), and the Heidenhain variant of Prion disease. It is unknown what predisposes these conditions to present as PCA. Given its rarity and variable presentations, misdiagnosis is common. We present a case of a 60-year-old woman with PCA who was initially undiagnosed. She measurably improved on donepezil and memantine suggesting AD as its pathogenesis.
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