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Case Report: Marchiafava-Bignami disease: anti-parietal cell antibodies as a potential etiological factor in a novel
Junhao Zhang1, Lizhen Wang1, Shuangfeng Yang2
1Department of Neurology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China.
Abstract:
Marchiafava-Bignami disease (MBD) represents a rare neurological disorder predominantly associated with chronic ethanol consumption and thiamine insufficiency. However, its possible correlation with cobalamin deficiency resulting from anti-parietal cell antibodies (APCA) remained inadequately characterized in the literature. Timely diagnosis and therapeutic intervention were critical for optimizing clinical outcomes. This case suggested that APCA screening and vitamin B12 assessment should be considered in the diagnostic workup of MBD, especially in patients without classic thiamine deficiency.
Insights
Marchiafava-Bignami disease (MBD) may be linked to cobalamin deficiency from anti-parietal cell antibodies (APCA). Consider APCA screening and vitamin B12 assessment in MBD diagnosis, particularly when thiamine deficiency is absent.
Area of Science:
- Neurology
- Internal Medicine
- Nutritional Science
Background:
- Marchiafava-Bignami disease (MBD) is a rare neurological condition.
- It is primarily linked to chronic alcohol use and thiamine deficiency.
- The role of cobalamin deficiency due to anti-parietal cell antibodies (APCA) in MBD is not well understood.
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