[A case of left posterior cortical atrophy presenting with kana-predominant reading impairment].

Q4 Medicine Clinical Neurology Pub Date : 2024-08-27 Epub Date: 2024-07-27 DOI:10.5692/clinicalneurol.cn-001907
Natsuki Nakatani, Daisuke Ono, Kosei Hirata, Kotaro Yoshioka, Hironobu Endo, Kenjiro Ono, Makoto Higuchi, Takanori Yokota
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Abstract

The patient was an 85-year-old man with a one-year history of difficulty reading kana. Neuropsychological evaluation revealed kana (phonogram)-selective reading impairment and kanji (ideogram)-dominant writing impairment. MRI revealed significant cerebral atrophy in the left occipital cortex, leading to the clinical diagnosis of posterior cortical atrophy (PCA). Cerebrospinal fluid amyloid β1-42 levels were reduced, and amyloid PET showed accumulation in the posterior cingulate cortex, precuneus, and frontal lobe. In contrast, tau PET showed no accumulation in the atrophied brain areas. Episodes of REM sleep behavior disorder and decreased uptake on meta-iodobenzylguanidine (MIBG) myocardial scintigraphy suggested the involvement of Lewy body pathology. PCA with distinct laterality has been rarely reported, and ‍this is the first case to present Kana-selective reading impairment and Kanji-dominant writing impairment with neurodegenerative background.

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[左后部皮质萎缩伴假名阅读障碍病例]。
患者是一名 85 岁的老人,有一年的假名阅读障碍病史。神经心理评估显示,患者存在假名(音标)选择性阅读障碍和汉字(表意文字)主导性书写障碍。核磁共振成像显示左枕叶皮质明显萎缩,临床诊断为后皮质萎缩(PCA)。脑脊液淀粉样蛋白β1-42水平降低,淀粉样蛋白PET显示后扣带回皮层、楔前区和额叶有积聚。与此相反,tau PET在萎缩的大脑区域没有显示出积聚。快速眼动睡眠行为障碍的发作和间碘苄基胍(MIBG)心肌闪烁照相摄取量的减少表明路易体病变也参与其中。PCA伴有明显偏侧的病例很少见,而‍这是第一例伴有神经退行性背景的汉字选择性阅读障碍和汉字优势性书写障碍的病例。
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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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