Coexistence of multiple sclerosis and brain tumors: a literature review.

A. Sirko, L. Dzyak, E. Chekha
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引用次数: 1

Abstract

Concurrent development of primary brain tumors and multiple sclerosis is quite rare. Only a few dozens of such comorbidity have been reported. Nevertheless, given the fact that such pathologies are characterized by similar clinical picture and neuroimaging findings, issues about diagnosis and differential diagnosis of such conditions often arise, which makes the problem relevant. A literature review was conducted using PubMed, by selecting articles on concurrent multiple sclerosis and brain tumors, particularly glial origin tumors, over the past 20 years (1989 to 2019). The search was performed in English, Russian, and Ukrainian using the following key words and terms: comorbidity, concomitance, multiple sclerosis, brain tumor, glioma, astrocytoma, glioblastoma. The analysis included all articles on etiology, pathogenesis, clinical picture, diagnosis, differential diagnosis, neuroimaging, and pathomorphological assessment. After identifying all the articles that met the inclusion criteria and removing duplicate data, 35 literature sources on concurrent primary brain tumors and multiple sclerosis were selected. The conclusion on whether concurrent primary brain tumors and multiple sclerosis develop randomly or have common pathophysiological mechanisms is still under discussion. Potential causes of pathogenesis of both diseases include viral infection, chronic inflammation, neoplastic transformation, and involvement of neurotropic growth factors. The likelihood that two processes, demyelinating and neoplastic, can develop in parallel will never be underestimated. In such cases, strong clinical suspicion arises due to atypical clinical picture characterized by aggressive and rapidly growing neurological symptoms such as aphasia, spastic hemiparesis, epileptic seizures, or signs of intracranial hypertension. In MRI diagnosis, pathological findings such as single lesion of more than 2 cm; mass effect, edema, signal amplification in the form of ring-shaped shadow are the reasons for a more thorough examination and applying additional diagnostic methods: CT, MR spectroscopy, PET, CSF tests to determine oligoclonal antibodies and other markers content, cerebral biopsy. According to the literature, cases of concurrent primary brain tumors and multiple sclerosis are rare though described. Atypical clinical signs, neuroimaging data, and cerebral biopsy which is currently considered as the only method for making accurate diagnosis are helpful in the diagnostic process.
多发性硬化症与脑肿瘤共存:文献综述。
原发性脑肿瘤和多发性硬化症同时发展是相当罕见的。只有几十个这样的合并症被报道过。然而,鉴于这些病理的特点是相似的临床图像和神经影像学结果,关于诊断和鉴别诊断的问题经常出现,这使得问题相关。在PubMed上进行了一项文献综述,选择了过去20年(1989年至2019年)关于多发性硬化症和脑肿瘤,特别是神经胶质源性肿瘤的文章。搜索以英语、俄语和乌克兰语进行,使用以下关键词和术语:合并症、合并症、多发性硬化症、脑肿瘤、胶质瘤、星形细胞瘤、胶质母细胞瘤。分析包括所有关于病因、发病机制、临床表现、诊断、鉴别诊断、神经影像学和病理形态学评估的文章。在确定所有符合纳入标准的文章并去除重复数据后,我们选择了35篇关于原发性脑肿瘤和多发性硬化症并发的文献。原发性脑肿瘤与多发性硬化症是随机发生还是有共同的病理生理机制,目前还没有定论。这两种疾病的潜在发病原因包括病毒感染、慢性炎症、肿瘤转化和嗜神经生长因子的参与。脱髓鞘和肿瘤这两个过程并行发展的可能性永远不会被低估。在这些病例中,由于不典型的临床表现,如失语、痉挛性偏瘫、癫痫发作或颅内高压症状等侵袭性和快速增长的神经系统症状,引起强烈的临床怀疑。在MRI诊断中,病理表现如单个病变大于2cm;肿块效应,水肿,环形阴影形式的信号放大是更彻底的检查和应用额外的诊断方法的原因:CT, MR光谱,PET, CSF测试以确定寡克隆抗体和其他标记物的含量,脑活检。据文献报道,原发性脑肿瘤和多发性硬化症同时发生的病例虽然有描述,但很少见。非典型临床症状、神经影像学资料和目前被认为是准确诊断的唯一方法的脑活检有助于诊断过程。
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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