揭示双重认知障碍:Marchiafava-Bignami病和可能的阿尔茨海默病的病例报告和文献综述。

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Floris Petru Iliuta, Mirela Manea, Aliss Madalina Mares, Corina Ioana Varlam, Constantin Alexandru Ciobanu, Adela Magdalena Ciobanu, Radu-Mihail Lacau, Mihnea Costin Manea
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引用次数: 0

摘要

阿尔茨海默病(AD)是最常见的痴呆症,特别是在65岁及以上的人群中。痴呆症也可能发生在45岁以下,被称为年轻发病痴呆(YOD),尽管这种情况比较少见。Marchiafava-Bignami病(MBD)是一种罕见的以胼胝体脱髓鞘和坏死为特征的疾病,主要影响慢性酒精使用的个体。我们报告一名49岁的女性,因大约四年前突然发作的多领域认知障碍而入院接受精神病学和神经学评估,其进展迅速,导致日常活动完全依赖他人。她的病史包括中度抑郁、长期饮酒和职业倦怠。心理评估显示严重的神经认知障碍。MRI扫描显示明显的双侧顶叶萎缩、海马萎缩和胼胝体脱髓鞘病变,与MBD一致。尽管最初的生物标志物不一致,但后来的测试显示tau蛋白升高,磷酸化tau蛋白和淀粉样蛋白- β,支持AD诊断。临床表现,结合神经影像学发现和慢性饮酒史,导致诊断为年轻发病的AD和慢性MBD。这个病例说明了诊断重叠神经退行性疾病的复杂性。MBD和AD的共存使治疗计划复杂化,需要多方面的方法解决神经退行性和营养方面的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling Dual Cognitive Disorders: A Case Report and Literature Review on Marchiafava-Bignami Disease and Possible Alzheimer's Disease.

Alzheimer's disease (AD) is the most prevalent form of dementia, particularly in those aged 65 and older. Dementia can also occur under age 45, known as young-onset dementia (YOD), although this is rarer. Marchiafava-Bignami disease (MBD) is a rare disorder characterized by demyelination and necrosis of the corpus callosum, primarily affecting individuals with chronic alcohol use. We present the case of a 49-year-old woman admitted for psychiatric and neurological evaluation due to a multidomain cognitive disorder with a sudden onset approximately four years prior, which progressed rapidly, resulting in complete dependence on others for daily activities. Her medical history included moderate depression, chronic alcohol consumption, and professional exhaustion. Psychological assessments revealed severe neurocognitive impairment. MRI scans highlighted significant bilateral parietal atrophy, hippocampal atrophy, and demyelinating lesions in the corpus callosum, consistent with MBD. Despite initial inconsistencies in biomarkers, later tests showed elevated tau protein, phosphorylated tau, and amyloid-beta, supporting an AD diagnosis. Clinical presentation, combined with neuroimaging findings and chronic alcohol consumption history, led to a diagnosis of AD with young onset and chronic MBD. This case illustrates the complexities involved in diagnosing overlapping neurodegenerative disorders. The coexistence of MBD and AD complicates the treatment plan, requiring a multifaceted approach addressing both neurodegenerative and nutritional aspects.

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