多发性硬化症中的皮质病理学

Cortical pathology in multiple sclerosis.

作者信息

Stadelmann Christine, Albert Monika, Wegner Christiane, Brück Wolfgang

机构信息

Institute of Neuropathology, University Medical Centre, Göttingen, Germany.

出版信息

Curr Opin Neurol. 2008 Jun;21(3):229-34. doi: 10.1097/01.wco.0000318863.65635.9a.

Abstract

PURPOSE OF REVIEW

Multiple sclerosis is the most common chronic, disabling central nervous system disease in young adults, characterized by inflammatory demyelinating white matter lesions with glial scar formation and axonal loss. Lately, evidence has accumulated that large areas of grey matter are affected in multiple sclerosis patients.

RECENT FINDINGS

Findings in post-mortem brain tissue support the notion that cortical demyelination is frequent and extensive, especially in patients with chronic multiple sclerosis. Cortical lesions differ from white matter lesions with respect to inflammatory cell infiltration, gliosis, and remyelination. Thus, differences in cortical and white matter lesion pathogenesis have been proposed. Experimental models suggest a decisive role for antimyelin antibodies in cortical demyelination. Topical studies focus on damage to neurons, dendrites, and synapses in cortical multiple sclerosis lesions. Improved imaging techniques for the detection of cortical lesions are currently developed and will provide the basis for future clinicopathological correlative studies.

SUMMARY

In summary, recent years have opened our eyes to the extensive grey matter involvement in multiple sclerosis. Studies on the pathogenesis of cortical demyelination, cortical damage, and repair will elucidate basic principles of multiple sclerosis lesion formation. However, more sensitive imaging tools are required to study the impact of cortical lesions on clinical symptoms, disability, and disease progression.

摘要

综述目的

多发性硬化是年轻成年人中最常见的慢性致残性中枢神经系统疾病,其特征为伴有胶质瘢痕形成和轴突丢失的炎性脱髓鞘白质病变。最近,越来越多的证据表明多发性硬化患者的大片灰质受到影响。

最新发现

尸检脑组织的研究结果支持皮质脱髓鞘常见且广泛的观点,尤其是在慢性多发性硬化患者中。皮质病变在炎症细胞浸润、胶质增生和再髓鞘化方面与白质病变不同。因此,有人提出皮质和白质病变发病机制存在差异。实验模型表明抗髓鞘抗体在皮质脱髓鞘中起决定性作用。局部研究聚焦于皮质多发性硬化病变中神经元、树突和突触的损伤。目前正在开发用于检测皮质病变的改进成像技术,这将为未来的临床病理相关性研究提供基础。

总结

总之,近年来我们已认识到多发性硬化中广泛的灰质受累情况。对皮质脱髓鞘、皮质损伤和修复发病机制的研究将阐明多发性硬化病变形成的基本原理。然而,需要更敏感的成像工具来研究皮质病变对临床症状、残疾和疾病进展的影响。

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