The coincidence of multiple sclerosis and primary vasculitis; from the bench of pathology to the bedside of treatment: a systematic review of case reports.

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY Neurological Sciences Pub Date : 2024-09-04 DOI:10.1007/s10072-024-07746-8
Melika Arab Bafrani, Hassan Asadigandomani, Naghmeh Abbasi Kasbi, Hora Heidari, Sharareh Eskandarieh
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Abstract

Introduction: Multiple sclerosis (MS) is a chronic, disabling neurodegenerative disease, leads to reduced quality of life. The increasing prevalence of MS around the world and its comorbidities increase its burden. Primary vasculitis subtypes, one of autoimmune diseases with different prevalence in different ages and genders, should be considered one of the important differential diagnosis in patients with MS. This study aims to verify the relationship between MS and primary vasculitis by conducting a systematic review.

Method: We searched PubMed, Scopus, EMBASE, Web of Science, and Google Scholar, from January 1974 to July 2023. We included original articles that reported characteristics of patients involved with any type of Primary Vasculitis with MS.

Result: From an initial 816 publications, 18 studies consisting of 18 individual patients from 14 countries with confirmed MS and one of different subtypes of primary vasculitis met the inclusion criteria. The female/male ratio was 0.38:1, the mean (SD) age was 40.44 (14.37) years with the range of 16 to 70 years old, and the relapsing/progressive ratio was 1.57:1. Most of them, 14 (77%) experienced MS before vasculitis, and mostly received Corticosteroids, interferon, cyclophosphamide, Glatiramer acetate as MS treatment. The concurrence of Takayasu Arteritis (2 cases), Polyarteritis Nodosa (2 cases), Churg-Strauss Syndrome (1 case), Wegener's Granulomatosis (2 cases), Microscopic Polyangiitis (1 case), Cutaneous leukocytoclastic vasculitis (5 cases), Good pasture's disease (5 cases) were reported with MS.

Conclusion: Our study suggested that different primary vasculitis can be an important comorbidity of MS and can mimic its symptoms and MRI. Any atypical syndrome for PwMS, whether clinical or radiological, must be evaluated in terms of other differential diagnoses including vasculitis.

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多发性硬化症与原发性血管炎的巧合;从病理学研究到床边治疗:病例报告的系统回顾。
简介多发性硬化症(MS)是一种慢性、致残性神经退行性疾病,会导致生活质量下降。多发性硬化症在全球的发病率不断上升,其并发症增加了患者的负担。原发性血管炎亚型是一种自身免疫性疾病,在不同年龄和性别有不同的发病率,应被视为多发性硬化症患者的重要鉴别诊断之一。本研究旨在通过系统综述验证多发性硬化症与原发性血管炎之间的关系:方法:我们检索了 1974 年 1 月至 2023 年 7 月期间的 PubMed、Scopus、EMBASE、Web of Science 和 Google Scholar。我们收录了报道任何类型原发性血管炎合并多发性硬化症患者特征的原创文章:结果:在最初的 816 篇文献中,有 18 项研究符合纳入标准,这些研究涉及来自 14 个国家的 18 名确诊为多发性硬化症的患者,他们都患有一种不同亚型的原发性血管炎。女性/男性比例为 0.38:1,平均(标清)年龄为 40.44 (14.37)岁,年龄范围为 16 至 70 岁,复发/进展比例为 1.57:1。其中14人(77%)在患血管炎前曾患多发性硬化症,大多接受皮质类固醇、干扰素、环磷酰胺、醋酸格拉替雷等治疗。有报告称,多发性硬化症患者同时患有高安动脉炎(2 例)、结节性多动脉炎(2 例)、丘格-斯特劳斯综合征(1 例)、韦格纳肉芽肿病(2 例)、显微镜下多血管炎(1 例)、皮肤白细胞胞浆细胞减少性血管炎(5 例)和好牧草病(5 例):我们的研究表明,不同的原发性血管炎可能是多发性硬化症的重要合并症,并可模拟其症状和磁共振成像。PwMS的任何非典型综合征,无论是临床表现还是影像学表现,都必须与包括血管炎在内的其他鉴别诊断进行评估。
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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来源期刊
Neurological Sciences
Neurological Sciences 医学-临床神经学
CiteScore
6.10
自引率
3.00%
发文量
743
审稿时长
4 months
期刊介绍: Neurological Sciences is intended to provide a medium for the communication of results and ideas in the field of neuroscience. The journal welcomes contributions in both the basic and clinical aspects of the neurosciences. The official language of the journal is English. Reports are published in the form of original articles, short communications, editorials, reviews and letters to the editor. Original articles present the results of experimental or clinical studies in the neurosciences, while short communications are succinct reports permitting the rapid publication of novel results. Original contributions may be submitted for the special sections History of Neurology, Health Care and Neurological Digressions - a forum for cultural topics related to the neurosciences. The journal also publishes correspondence book reviews, meeting reports and announcements.
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