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A combined post-mortem magnetic resonance imaging and quantitative histological study of multiple sclerosis pathology.多发性硬化症病理学的联合死后磁共振成像和定量组织学研究。
Brain. 2012 Oct;135(Pt 10):2938-51. doi: 10.1093/brain/aws242.
2
Neuromyelitis optica lesions may inform multiple sclerosis heterogeneity debate.视神经脊髓炎病灶可能为多发性硬化异质性争论提供信息。
Ann Neurol. 2012 Sep;72(3):385-94. doi: 10.1002/ana.23621.
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No MRI evidence of cortical lesions in neuromyelitis optica.视神经脊髓炎中无皮质病变的 MRI 证据。
Neurology. 2012 Oct 16;79(16):1671-6. doi: 10.1212/WNL.0b013e31826e9a96. Epub 2012 Sep 19.
4
Meningeal inflammation plays a role in the pathology of primary progressive multiple sclerosis.脑膜炎症在原发性进行性多发性硬化症的病理学中起作用。
Brain. 2012 Oct;135(Pt 10):2925-37. doi: 10.1093/brain/aws189. Epub 2012 Aug 20.
5
Distinct lesion morphology at 7-T MRI differentiates neuromyelitis optica from multiple sclerosis.7T MRI 显示出不同的病变形态,可将视神经脊髓炎与多发性硬化区分开来。
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6
Potassium channel KIR4.1 as an immune target in multiple sclerosis.钾通道 KIR4.1 作为多发性硬化症的免疫靶点。
N Engl J Med. 2012 Jul 12;367(2):115-23. doi: 10.1056/NEJMoa1110740.
7
Association between pathological and MRI findings in multiple sclerosis.多发性硬化的病理与 MRI 表现的相关性。
Lancet Neurol. 2012 Apr;11(4):349-60. doi: 10.1016/S1474-4422(12)70003-0. Epub 2012 Mar 19.
8
Meningeal and cortical grey matter pathology in multiple sclerosis.多发性硬化症的脑膜和皮质灰质病理学。
BMC Neurol. 2012 Mar 7;12:11. doi: 10.1186/1471-2377-12-11.
9
NADPH oxidase expression in active multiple sclerosis lesions in relation to oxidative tissue damage and mitochondrial injury.NADPH 氧化酶在活动期多发性硬化病变中的表达与氧化组织损伤和线粒体损伤的关系。
Brain. 2012 Mar;135(Pt 3):886-99. doi: 10.1093/brain/aws012.
10
Pathology of demyelinating diseases.脱髓鞘疾病的病理学。
Annu Rev Pathol. 2012;7:185-217. doi: 10.1146/annurev-pathol-011811-132443.

多发性硬化症的病理学:我们目前的进展如何?

Pathology of multiple sclerosis: where do we stand?

作者信息

Popescu Bogdan F Gh, Pirko Istvan, Lucchinetti Claudia F

机构信息

Department of Neurology, Mayo Clinic College of Medicine, 200 First St Southwest, Rochester, MN 55905, USA.

出版信息

Continuum (Minneap Minn). 2013 Aug;19(4 Multiple Sclerosis):901-21. doi: 10.1212/01.CON.0000433291.23091.65.

DOI:10.1212/01.CON.0000433291.23091.65
PMID:23917093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3915566/
Abstract

PURPOSE OF REVIEW

This article summarizes the pathologic features of multiple sclerosis (MS) and other inflammatory demyelinating diseases and discusses neuropathologic studies that have yielded novel insights into potential mechanisms of demyelination.

RECENT FINDINGS

The pathologic hallmark of MS consists of focal demyelinated plaques within the CNS, with variable degrees of inflammation, gliosis, and neurodegeneration. Active MS lesions show a profound pathologic heterogeneity with four major patterns of immunopathology, suggesting that the targets of injury and mechanisms of demyelination in MS may be different in different disease subgroups. Recent pathologic studies have suggested that the subarachnoid space and cortex may be initial sites and targets of the MS disease process, that inflammatory cortical demyelination is present early in MS, and that meningeal inflammation may drive cortical and white matter injury in some MS patients.

SUMMARY

MS is heterogeneous with respect to clinical, genetic, radiographic, and pathologic features; surrogate MRI, clinical, genetic, serologic, and/or CSF markers for each of the four immunopatterns need to be developed in order to recognize them in the general nonbiopsied MS population. Inflammatory cortical demyelination is an important early event in the pathogenesis of MS and may be driven by meningeal inflammation. These observations stress the importance of developing imaging techniques able to capture early inflammatory cortical demyelination in order to better understand the disease pathogenesis and to determine the impact of potential disease-modifying therapies on the cortex.

摘要

综述目的

本文总结了多发性硬化(MS)及其他炎性脱髓鞘疾病的病理特征,并讨论了对脱髓鞘潜在机制有新见解的神经病理学研究。

最新发现

MS的病理特征是中枢神经系统内出现局灶性脱髓鞘斑块,伴有不同程度的炎症、胶质增生和神经变性。活动性MS病变表现出明显的病理异质性,有四种主要的免疫病理学模式,这表明MS中损伤靶点和脱髓鞘机制在不同疾病亚组中可能不同。最近的病理研究表明,蛛网膜下腔和皮质可能是MS疾病进程的初始部位和靶点,炎性皮质脱髓鞘在MS早期就存在,并且脑膜炎症可能在一些MS患者中驱动皮质和白质损伤。

总结

MS在临床、遗传、影像学和病理特征方面具有异质性;需要开发针对四种免疫模式中每种模式的替代MRI、临床、遗传、血清学和/或脑脊液标志物,以便在一般未进行活检的MS人群中识别它们。炎性皮质脱髓鞘是MS发病机制中的一个重要早期事件,可能由脑膜炎症驱动。这些观察结果强调了开发能够捕捉早期炎性皮质脱髓鞘的成像技术的重要性,以便更好地理解疾病发病机制,并确定潜在疾病修饰疗法对皮质的影响。