迟发性语义性痴呆伴原发性颞叶萎缩1例。

IF 1.7
Yuta Sudo, Masashi Tamura, Kenjiro Nakayama, Kiyotaka Nemoto, Osamu Yokota, Kenji Tagai, Hironobu Endo, Takahiko Tokuda, Makoto Higuchi, Kentaro Hatano, Tetsuaki Arai
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引用次数: 0

摘要

语义性痴呆(SD)是一种以语义记忆丧失为特征的痴呆,典型表现为左侧颞叶萎缩和额颞叶变性,伴TDP-43 (FTLD-TDP) C型病理。然而,非典型变异,如迟发性或右侧萎缩,表现出相当大的病理多样性。我们报告了一位81岁的非典型SD女性,她表现为命名障碍,轻度单词理解障碍和面孔失认症。脑部MRI显示杏仁核、海马体和前颞叶右侧萎缩。脑脊液分析显示a β水平正常,提示非阿尔茨海默病病理。Tau PET成像显示右侧前颞叶高信号,与原发性脑病一致。患者的临床表现和影像学表现,特别是杏仁核和海马的萎缩,以及交流能力的保留,提高了嗜银性谷物病(AGD)作为潜在病理的可能性。本病例强调了分子成像在诊断非典型SD中的重要性。这表明AGD应该被认为是不典型SD病例的潜在病理,特别是那些晚发和右侧占优势的病例。需要更长时间的随访和最终的尸检来确认病理诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Late-Onset Semantic Dementia With Right-Predominant Temporal Lobe Atrophy due to Primary Tauopathy.

Semantic dementia (SD) is a type of dementia characterized by a loss of semantic memory, typically presenting with left-predominant temporal lobe atrophy and a frontotemporal lobar degeneration with TDP-43 (FTLD-TDP) type C pathology. However, atypical variants, such as those with a late-onset or right-predominant atrophy, exhibit considerable pathological diversity. We report an 81-year-old woman with atypical SD who presented with impaired naming, mild word comprehension deficits, and prosopagnosia. Brain MRI revealed right-predominant atrophy in the amygdala, hippocampus, and anterior temporal lobes. Cerebrospinal fluid analysis showed a normal Aβ level, suggesting a non-Alzheimer's disease pathology. Tau PET imaging demonstrated a high signal in the right anterior temporal lobe, consistent with primary tauopathy. The patient's clinical presentation and imaging findings, particularly the atrophy in the amygdala and hippocampus, as well as the preserved communication ability, raised the possibility of argyrophilic grain disease (AGD) as the underlying pathology. This case highlights the importance of molecular imaging in diagnosing atypical SD. It suggests that AGD should be considered a possible underlying pathology for atypical SD cases, particularly those with late onset and right-sided predominance. A longer follow-up and eventual autopsy would be necessary to confirm the pathological diagnosis.

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