Dementia with Grains: A Clinical Mimic of Dementia with Lewy Bodies - Case Report.

IF 0.4 Q4 CLINICAL NEUROLOGY
Case Reports in Neurology Pub Date : 2025-11-17 eCollection Date: 2025-01-01 DOI:10.1159/000549534
Sarah L Gardiner, Nina L Fransen, Annemieke J M Rozemuller, Evelien W Lemstra
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Abstract

Introduction: Dementia characterized by the accumulation of argyrophilic grains (AGs) in neurons as sole neuropathology at autopsy is known as dementia with grains (DG). The clinical features of DG include progressive memory disturbances and behavioral changes. Recently however, cases of DG presenting with parkinsonism were also described. Here, we report the first case of DG mimicking dementia with Lewy bodies.

Case presentation: A 72-year-old male patient was seen at our outpatient memory clinic with progressive complaints in multiple cognitive domains (memory, orientation, praxis, and executive function), fluctuations in arousal and behavioral changes. In addition, he reported neuropsychiatric symptoms, including a depressed mood and visual hallucinations. During neurological examination, he demonstrated bilateral rigidity and bradykinesia with a right-sided predominance. These symptoms in combination with decreased striatal uptake of tracer on a 123I-FP-CIT-SPECT scan led to the clinical diagnosis of probable mild dementia with Lewy bodies. Treatment was with rivastigmine, and levodopa/benserazide was initiated. Over the years, cognitive and motor function only slowly progressed. Autopsy was performed after passing. Neuropathological findings included dot-like and comma-shaped tau-positive structures, indicative of AGs, spread throughout the limbic but also the nigrostriatal system. No co-pathology and in particular no alpha-synucleinopathy was present. Consequently, patient's diagnosis was posthumously revised to DG.

Conclusion: Here, we present the first known case of DG clinically mimicking dementia with Lewy bodies. Our findings support the notion that parkinsonism should be included in the clinical phenotype of DG and that DG should be considered more often as diagnosis, when the clinical presentation is atypical.

Abstract Image

Abstract Image

痴呆与颗粒:痴呆与路易体临床模拟-病例报告。
以神经元中亲银颗粒(AGs)的积累为特征的痴呆症是尸检时唯一的神经病理学,被称为颗粒痴呆(DG)。DG的临床特征包括进行性记忆障碍和行为改变。然而,最近也出现了以帕金森病为表现的DG病例。在这里,我们报告第一例DG模仿痴呆与路易体。病例介绍:一名72岁男性患者在我们的记忆门诊就诊,在多个认知领域(记忆、定向、实践和执行功能)出现进行性主诉,觉醒波动和行为改变。此外,他还报告了神经精神症状,包括情绪低落和视觉幻觉。在神经学检查中,他表现为双侧僵硬和运动迟缓,以右侧为主。这些症状与123I-FP-CIT-SPECT扫描纹状体示踪剂摄取减少相结合,导致临床诊断可能为路易体轻度痴呆。治疗采用利瓦斯汀,左旋多巴/苯塞拉肼。多年来,认知和运动功能只是缓慢发展。死亡后进行尸检。神经病理学发现包括点状和逗号状的tau阳性结构,表明AGs,分布于整个边缘和黑质纹状体系统。无合并病理,特别是无α -突触核蛋白病。因此,患者死后诊断为DG。结论:在这里,我们提出了第一例DG临床模仿路易体痴呆的病例。我们的研究结果支持这样一种观点,即帕金森病应包括在DG的临床表型中,当临床表现不典型时,DG应更多地被视为诊断。
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来源期刊
Case Reports in Neurology
Case Reports in Neurology Medicine-Neurology (clinical)
CiteScore
1.50
自引率
0.00%
发文量
67
审稿时长
14 weeks
期刊介绍: This new peer-reviewed online-only journal publishes original case reports covering the entire spectrum of neurology. Clinicians and researchers are given a tool to disseminate their personal experience to a wider public as well as to review interesting cases encountered by colleagues all over the world. To complement the contributions supplementary material is welcomed. The reports are searchable according to the key words supplied by the authors; it will thus be possible to search across the entire growing collection of case reports with universally used terms, further facilitating the retrieval of specific information. Following the open access principle, the entire contents can be retrieved at no charge, guaranteeing easy access to this valuable source of anecdotal information at all times.
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