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[一例提示血管源性水肿的马基亚法瓦-比尼亚米病病例]

[A case of Marchiafava-Bignami disease suggesting vasogenic edema].

作者信息

Nakamura Yuki, Matsuya Manabu, Ikeda Kazuna, Tsuda Reiko, Ariyoshi Naomitsu, Shimohama Shun

机构信息

Department of Neurology, Saiseikai Otaru Hospital.

出版信息

Rinsho Shinkeigaku. 2016;56(1):17-22. doi: 10.5692/clinicalneurol.cn-000774. Epub 2015 Nov 30.

Abstract

A 61-year-old alcoholic man was admitted to our hospital because of disturbance of consciousness. He also exhibited external ophthalmoplegia, diplopia and mild rigidity, but tendon reflex was normal. On brain MRI, diffusion weighted images (DWI) and apparent diffusion coefficient (ADC) map depicted high intensity in the splenium of the corpus callosum. DWI showed high intensity, but ADC map depicted iso-intensity in bilateral precentral gyri. Marchiafava-Bignami disease (MBD) was diagnosed. After intravenous drip of vitamin, his symptoms improved rapidly and the abnormal MRI findings in the splenium of the corpus callosum and bilateral precentral gyri disappeared gradually. MBD is pathologically characterized by demyelination and necrosis in the corpus callosum, which are generally caused by cytotoxic edema. Our case suggests that vasogenic edema may occur at the early stage of the MBD.

摘要

一名61岁的酗酒男性因意识障碍入住我院。他还表现出眼球外肌麻痹、复视和轻度强直,但腱反射正常。脑部磁共振成像(MRI)检查中,扩散加权成像(DWI)和表观扩散系数(ADC)图显示胼胝体压部呈高强度信号。DWI显示高强度信号,但ADC图显示双侧中央前回呈等强度信号。确诊为马基亚法瓦-比尼亚米病(MBD)。静脉滴注维生素后,他的症状迅速改善,胼胝体压部和双侧中央前回的异常MRI表现逐渐消失。MBD的病理特征是胼胝体脱髓鞘和坏死,通常由细胞毒性水肿引起。我们的病例表明,MBD早期可能发生血管源性水肿。

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