Marburg Variant of Multiple Sclerosis: A Case Report

Varada Vikas Ghadge, Amol Gowardhan Bondre, Tilottama Parate, Rahul Bhiwgade
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Abstract

Multiple sclerosis (MS) is a demyelinating disorder with central nervous system (CNS) involvement, leading to varied presentations. It is an autoimmune disease characterised by chronic inflammation, demyelination, gliosis (plaques or scarring) and neuronal loss with relapsing or progressive course. MS plaques typically develop at different times and in different CNS locations (i.e., MS is said to be disseminated in time and space). The clinical course is extremely variable, ranging from a relatively benign condition to a rapidly evolving and incapacitating disease requiring profound lifestyle adjustments. MacDonald’s criteria are frequently used to diagnose MS. Rapidly, evolving severe forms of MS such as Marburg’s variant and Balo’s concentric sclerosis account for <4% of total incidence of MS. The clinical course is rapid and often fatal. The exact aetiology behind this malignant nature of Marburg’s variant MS is unknown. In this case report, we will be discussing one such rare presentation of Marburg variant of MS.
马尔堡变异体多发性硬化症1例报告
多发性硬化症(MS)是一种涉及中枢神经系统(CNS)的脱髓鞘疾病,导致多种表现。它是一种自身免疫性疾病,特征为慢性炎症、脱髓鞘、神经胶质瘤(斑块或瘢痕)和神经元丧失,病程复发或进展。多发性硬化症斑块通常在不同时间和不同中枢神经系统位置发生(即多发性硬化症在时间和空间上具有弥散性)。临床病程变化多端,从相对良性的病情到迅速发展的致残疾病,需要对生活方式进行深刻的调整。MacDonald的诊断标准常被用于诊断多发性硬化症,迅速发展的严重形式的多发性硬化症,如马尔堡变型和Balo同心圆硬化症占MS总发病率的4%以下。马尔堡变异型多发性硬化症恶性本质背后的确切病因尚不清楚。在这个病例报告中,我们将讨论这样一个罕见的马尔堡变异多发性硬化症的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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