Etiology and characteristics of pseudotumoral lesions and tumefactive demyelination in multiple sclerosis

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Multiple sclerosis and related disorders Pub Date : 2024-11-12 DOI:10.1016/j.msard.2024.106168
Olivera Tamas , Marija Kovacevic , Nikola Veselinovic , Maja Budimkic , Vanja Jovicevic , Nikola Momcilovic , Jelena Drulovic , Sarlota Mesaros
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Abstract

Introduction

Cerebral pseudotumoral lesions (CPTL) (>2cm) on magnetic resonance imaging (MRI) may pose a clinical challenge. A majority will occur in the context of multiple sclerosis (MS) – also referred to as tumefactive demyelinating lesions (TDL). The aim of this study was to define and analyze clinical, MRI, and paraclinical data for MS and non-MS patients.

Methods

This prospective study included adult patients with CPTL on brain MRI referred to the Neurology Clinic, Belgrade as a tertiary University Center (2019–2023) for clinical workup and treatment. Demographic, clinical, MRI, and paraclinical data were reviewed.

Results

This study included 75 patients, of which 58.7 % had MS. Fourteen patients had previously been diagnosed with MS, while 30 (68.2 %) received the diagnosis of MS in the later course. The concordance of initial and final diagnoses was 52 %. Relapsing disease (p < 0.001) and brainstem presentation (p = 0.039) were significantly more common in MS patients. Headache (p = 0.008) and lethal outcome (p = 0.014) were significantly more common in the non-MS group. Lesions were ring-like more frequently in the MS group (p < 0.001), while patients in the non-MS group frequently displayed infiltrative (p = 0.001) and nonspecific lesions (p = 0.002). The presence of headache and megacystic morphology was associated with the presence of pathology other than MS while the relapsing disease was in favor of MS.

Conclusion

Multiple sclerosis was the most common cause of CPTL. Headache, relapsing course of disease, and megacystic morphology may help discern MS from non-MS pathology. These findings should be challenged in future studies examining larger cohorts.
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多发性硬化症假瘤性病变和肿瘤活性脱髓鞘的病因和特征。
简介:磁共振成像(MRI)上的脑假瘤病变(CPTL)(>2 厘米)可能会给临床带来挑战。其中大部分会发生在多发性硬化症(MS)中,也称为肿瘤活动性脱髓鞘病变(TDL)。本研究旨在定义和分析多发性硬化症和非多发性硬化症患者的临床、核磁共振成像和辅助临床数据:这项前瞻性研究纳入了转诊至贝尔格莱德神经病学诊所作为三级大学中心(2019-2023 年)进行临床检查和治疗的脑磁共振成像显示 CPTL 的成年患者。研究回顾了人口统计学、临床、磁共振成像和辅助临床数据:本研究共纳入 75 名患者,其中 58.7% 患有多发性硬化症。14名患者曾被诊断为多发性硬化症,30名患者(68.2%)在后期病程中被诊断为多发性硬化症。最初诊断和最终诊断的一致性为 52%。复发性疾病(p < 0.001)和脑干表现(p = 0.039)在多发性硬化症患者中明显更为常见。在非多发性硬化症组中,头痛(p = 0.008)和致命结果(p = 0.014)明显更常见。多发性硬化症组患者的病变多呈环状(p < 0.001),而非多发性硬化症组患者则多呈浸润性(p = 0.001)和非特异性病变(p = 0.002)。头痛和巨囊形态的出现与多发性硬化症以外的病变有关,而复发性疾病则有利于多发性硬化症:结论:多发性硬化症是 CPTL 最常见的病因。头痛、复发性病程和巨囊形态可能有助于鉴别多发性硬化症和非多发性硬化症病理。这些发现应在今后更大规模的研究中加以验证。
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来源期刊
CiteScore
5.80
自引率
20.00%
发文量
814
审稿时长
66 days
期刊介绍: Multiple Sclerosis is an area of ever expanding research and escalating publications. Multiple Sclerosis and Related Disorders is a wide ranging international journal supported by key researchers from all neuroscience domains that focus on MS and associated disease of the central nervous system. The primary aim of this new journal is the rapid publication of high quality original research in the field. Important secondary aims will be timely updates and editorials on important scientific and clinical care advances, controversies in the field, and invited opinion articles from current thought leaders on topical issues. One section of the journal will focus on teaching, written to enhance the practice of community and academic neurologists involved in the care of MS patients. Summaries of key articles written for a lay audience will be provided as an on-line resource. A team of four chief editors is supported by leading section editors who will commission and appraise original and review articles concerning: clinical neurology, neuroimaging, neuropathology, neuroepidemiology, therapeutics, genetics / transcriptomics, experimental models, neuroimmunology, biomarkers, neuropsychology, neurorehabilitation, measurement scales, teaching, neuroethics and lay communication.
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