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马基亚法瓦-比尼亚米病:一例报告。

Marchiafava-Bignami disease: a case report.

作者信息

Pasutharnchat Nath, Phanthumchinda Kammant

机构信息

Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 2002 Jun;85(6):742-6.

Abstract

Marchiafava-Bignami Disease (MBD) is a rare, severe and usually fatal neurological disorder associated with chronic alcoholism. Previously, the definite diagnosis was confirmed at the autopsy. After the era of modern imaging technology, diagnosis was based on clinical profiles, history of alcoholism and specific location of pathology in corpus the callosum demonstrated by MRI. The authors reported a case of MBD in a 41 year-old alcoholic Thai male who presented with acute confusion and ataxia. MRI of the brain demonstrated demyelination, edema and necrosis of the corpus callosum with extensive symmetrical subcortical white matter lesions. He had a dramatic recovery after treatment with intravenous thiamine. Follow-up MRI revealed atrophic and cystic changes of the corpus callosum and almost complete resolution of the subcortical lesions. Recently, 15 cases of MBD with specific corpus callosal lesion, demonstrated by MRI, were published in the English literature. All had a favorable outcome after treatment with thiamine. Only one case had extensive extracallosal lesions and this case also had a good recovery after treatment. Now, MBD is not a fatal disease and early diagnosis and treatment are crucial.

摘要

马基亚法瓦-比尼亚米病(MBD)是一种与慢性酒精中毒相关的罕见、严重且通常致命的神经系统疾病。以前,明确诊断需在尸检时才能证实。在现代成像技术时代之后,诊断基于临床特征、酒精中毒史以及MRI显示的胼胝体特定病理位置。作者报告了一例41岁的泰国男性酒精中毒患者,该患者出现急性意识模糊和共济失调。脑部MRI显示胼胝体脱髓鞘、水肿和坏死,伴有广泛对称性皮质下白质病变。经静脉注射硫胺素治疗后,他有显著恢复。随访MRI显示胼胝体萎缩和囊性改变,皮质下病变几乎完全消退。最近,英文文献发表了15例经MRI证实有特定胼胝体病变的MBD病例。所有患者经硫胺素治疗后预后良好。只有一例有广泛的胼胝体外病变,该病例治疗后也恢复良好。现在,MBD已不是致命疾病,早期诊断和治疗至关重要。

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