Marchiafava-Bignami病的死前放射学和组织病理学表现。

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Leyla Canbeldek, Raquel T Yokoda, Lakshmi S Kulumani Mahadevan, Yamato Suemitsu, Jorge Samanamud, Cheyanne C Slocum, Carolina Maldonado-Díaz, Satomi Hiya, Kevin Clare, Raymund L Yong, Melissa Umphlett, Nadejda M Tsankova, John F Crary, Jamie M Walker, Thomas P Naidich, Timothy E Richardson
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引用次数: 0

摘要

Marchiafava-Bignami病(MBD)是一种罕见的疾病,以脱髓鞘和胼胝体囊性坏死为特征;它通常见于慢性酒精中毒,但也可能发生在严重营养不良的情况下。临床特征包括精神状态改变、意识丧失、构音障碍、痉挛、共济失调和癫痫发作。据我们所知,文献中仅报道了1例死前组织学的MBD。在此,我们描述了2例新的与MBD一致的胼胝体脱髓鞘病例的临床、放射学和组织病理学特征,这些病例是在死前活检中发现的;1例与慢性酒精中毒有关,另1例与严重营养不良有关。影像学检查显示,最初病变累及胼胝体的全层,后来演变为胼胝体中部三分之一的特征性线性坏死区。在这两例患者中,有额外的证据表明胼胝体外受累。两例患者的活检均显示大量巨噬细胞细胞质中有髓鞘碎片,轴突相对保存,尽管在巨噬细胞聚集最密集的区域有一些轴突丢失。这些发现突出了2例活检证实的MBD的临床和影像学进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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来源期刊
CiteScore
5.40
自引率
6.20%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Journal of Neuropathology & Experimental Neurology is the official journal of the American Association of Neuropathologists, Inc. (AANP). The journal publishes peer-reviewed studies on neuropathology and experimental neuroscience, book reviews, letters, and Association news, covering a broad spectrum of fields in basic neuroscience with an emphasis on human neurological diseases. It is written by and for neuropathologists, neurologists, neurosurgeons, pathologists, psychiatrists, and basic neuroscientists from around the world. Publication has been continuous since 1942.
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