Antemortem radiologic and histopathologic presentation of Marchiafava-Bignami disease

Marchiafava-Bignami disease (MBD) is a rare disorder, characterized by demyelination and cystic necrosis of the corpus callosum; it is typically seen in the setting of chronic alcoholism but may also occur with severe malnutrition. Clinical features include altered mental status, loss of consciousness, dysarthria, spasticity, ataxia, and seizures. To our knowledge, only 1 case of MBD with antemortem histology has been reported in the literature. Herein, we describe the clinical, radiologic, and histopathologic features of 2 new cases with corpus callosum demyelination consistent with MBD that were identified on antemortem biopsy; 1 was related to chronic alcoholism and the other was in the setting of severe malnutrition. Imaging studies showed that the initial lesions involved the full thickness of the corpus callosum with later evolution into the characteristic linear zone of necrosis in the mid-third of the corpus callosum. There was additional evidence of extracallosal involvement in both patients. Biopsies in both patients demonstrated numerous macrophages with myelin debris in their cytoplasm and relative axonal preservation, although there was some axonal loss in areas with the densest collection of macrophages. These findings highlight the clinical and radiographic progression in 2 cases of biopsy-proven MBD.

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Publication Details

Journal
Journal of Neuropathology & Experimental Neurology
Published
2025-06-24
DOI
https://doi.org/10.1093/jnen/nlaf074
Primary Topic
Infectious Encephalopathies and Encephalitis
Type
article
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article

Antemortem radiologic and histopathologic presentation of Marchiafava-Bignami disease

Yamato Suemitsu, Kevin Clare, Carolina Maldonado‐Díaz, Raymund L. Yong et al.
Journal of Neuropathology & Experimental Neurology
Infectious Encephalopathies and Encephalitis
article

Antemortem radiologic and histopathologic presentation of Marchiafava-Bignami disease

Yamato Suemitsu, Kevin Clare, Carolina Maldonado‐Díaz, Raymund L. Yong, Nadejda M. Tsankova, Thomas P. Naidich, Connie Slocum, Leyla Canbeldek, Timothy E. Richardson, Satomi Hiya, John F. Crary, Lakshmi Shree Kulumani Mahadevan, Melissa Umphlett, Jorge Samanamud, Jamie M. Walker, Raquel T. Yokoda
article en

Abstract

Marchiafava-Bignami disease (MBD) is a rare disorder, characterized by demyelination and cystic necrosis of the corpus callosum; it is typically seen in the setting of chronic alcoholism but may also occur with severe malnutrition. Clinical features include altered mental status, loss of consciousness, dysarthria, spasticity, ataxia, and seizures. To our knowledge, only 1 case of MBD with antemortem histology has been reported in the literature. Herein, we describe the clinical, radiologic, and histopathologic features of 2 new cases with corpus callosum demyelination consistent with MBD that were identified on antemortem biopsy; 1 was related to chronic alcoholism and the other was in the setting of severe malnutrition. Imaging studies showed that the initial lesions involved the full thickness of the corpus callosum with later evolution into the characteristic linear zone of necrosis in the mid-third of the corpus callosum. There was additional evidence of extracallosal involvement in both patients. Biopsies in both patients demonstrated numerous macrophages with myelin debris in their cytoplasm and relative axonal preservation, although there was some axonal loss in areas with the densest collection of macrophages. These findings highlight the clinical and radiographic progression in 2 cases of biopsy-proven MBD.

Journal of Neuropathology & Experimental NeurologyVol. 84(11)
Albert Einstein College of Medicine (US), Montefiore Medical Center (US), Icahn School of Medicine at Mount Sinai (US)
Zero hunger
Openalex Percentile: Top 81%
Infectious Encephalopathies and Encephalitis
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