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马奇亚法瓦-比尼亚米病:1例亚急性病例报告。

Marchiafava-Bignami Disease: Report of a Subacute Case.

作者信息

Castro Ivo, Cardoso João, Esteves Cristina, Figueiredo Adelaide

机构信息

Department of Internal Medicine, Hospital Distrital de Santarém, Santarém, PRT.

出版信息

Cureus. 2023 Feb 6;15(2):e34692. doi: 10.7759/cureus.34692. eCollection 2023 Feb.

Abstract

Marchiafava-Bignami disease (MBD) is rare and often associated with chronic alcohol consumption; however, cases have been described in non-alcoholic patients with nutritional deficits. This disease manifests itself through an array of neurological signs and symptoms, from mild dysarthria or mild confusion to coma and death, and can present acutely, subacutely, or chronically, depending on their severity. The evolution of imaging technology makes magnetic resonance imaging (MRI) the gold standard for the diagnosis of this disease, although computed tomography (CT) scan is usually in the first line owing to its greater availability. The main feature for the diagnosis of MBD by brain MRI is the identification of areas of demyelination and necrosis of the corpus callosum. We report a 55-year-old male with subacute neurological deterioration whose MRI demonstrated atrophy and demyelination of the corpus callosum.

摘要

马基亚法瓦-比尼亚米病(MBD)较为罕见,常与长期饮酒有关;然而,在有营养缺乏的非酒精性患者中也有病例报道。这种疾病通过一系列神经体征和症状表现出来,从轻度构音障碍或轻度意识模糊到昏迷和死亡,根据严重程度可急性、亚急性或慢性发作。成像技术的发展使磁共振成像(MRI)成为诊断该病的金标准,尽管计算机断层扫描(CT)由于其可用性更高通常作为一线检查。脑部MRI诊断MBD的主要特征是识别胼胝体的脱髓鞘和坏死区域。我们报告一例55岁男性,出现亚急性神经功能恶化,其MRI显示胼胝体萎缩和脱髓鞘。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6b8/9995083/a486b1d175e4/cureus-0015-00000034692-i01.jpg

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