Challenges in the Diagnosis of Multiple Sclerosis: A Case Report.

IF 0.6 Q3 Medicine
Acta Medica Lituanica Pub Date : 2026-01-01 Epub Date: 2026-07-22 DOI:10.15388/Amed.2026.33.1.20
Kristina Galinytė, Gintarė Butenytė, Gintarė Žemgulytė, Jurgita Makštienė, Renata Balnytė
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引用次数: 0

Abstract

Introduction: : Multiple sclerosis (MS) may present as a tumor-like, or tumefactive demyelinating lesion, that is indistinguishable clinically and radiologically from a brain tumor. This poses a diagnostic challenge.

Case presentation: We present a case report of a 23-year-old woman who was hospitalized in the Neurosurgery Department for biopsy of a brain mass. She had been diagnosed with Hodgkin's lymphoma at the age of 12, underwent surgery and chemotherapy, and had been in remission ever since. During her annual follow-up a magnetic resonance imaging (MRI) of the brain was performed that revealed a lesion in the right temporal lobe. It was interpreted as central nervous system (CNS) lymphoma. Before arranged neurosurgical intervention, a follow-up MRI scan revealed multiple new small lesions in both hemispheres. Biopsy was not performed, and the patient was referred to the Neurology Department for clarification of the diagnosis. No abnormalities were detected in the tests performed. Cerebrospinal fluid (CSF) was not tested due to the patient's refusal to repeat the unsuccessful procedure. The patient was discharged from the hospital. Three months later, she arrived at the Emergency Department abroad with impaired coordination and hypoesthesia on the right side of the body. Two MRI scans revealed a new lesion in the left posterior periventricular area. CNS lymphoma was suspected again. The patient received treatment with levetiracetam and dexamethasone. Upon her return, an MRI scan was repeated, which revealed an enlargement of the lesion. CSF testing showed indistinct oligoclonal bands. As CNS lymphoma could not be excluded, a lesion biopsy was performed after discontinuation of the steroids therapy. Histological examination excluded malignancy. Later, an MRI scan was repeated; it showed two new contrast-enhancing lesions. Relapsing-remitting multiple sclerosis (RRMS) diagnosis was confirmed, and treatment with disease-modifying therapies (DMTs) was planned.

Conclusions: Open-ring enhancement with little or no mass effect on MRI suggests a tumefactive demyelinating lesion (TDL). Moreover, TDLs tend to have a lower relative cerebral blood volume, and higher minimum and average apparent diffusion coefficient values compared to CNS lymphomas. Flow cytometry shows a monotypic B lymphoid population in cases of CNS lymphoma, not in MS.

多发性硬化症诊断的挑战:1例报告。
简介:多发性硬化症(MS)可能表现为肿瘤样或肿瘤性脱髓鞘病变,在临床和影像学上与脑肿瘤难以区分。这给诊断带来了挑战。病例报告:我们报告了一位23岁的女性,她因脑肿块活检而在神经外科住院。她在12岁时被诊断出患有霍奇金淋巴瘤,接受了手术和化疗,此后病情一直在缓解。在她的年度随访期间,进行了大脑磁共振成像(MRI),发现右侧颞叶有病变。诊断为中枢神经系统淋巴瘤。在安排神经外科干预之前,后续MRI扫描显示双脑半球有多个新的小病变。没有进行活检,患者被转到神经内科以澄清诊断。在执行的测试中未检测到异常。由于患者拒绝重复不成功的手术,未检测脑脊液(CSF)。病人出院了。三个月后,她来到国外急诊科,身体右侧协调能力受损,感觉减退。两次MRI扫描显示左侧后心室周围区域有新的病变。再次怀疑中枢神经系统淋巴瘤。患者给予左乙拉西坦和地塞米松治疗。在她回来后,再次进行核磁共振扫描,发现病变扩大。脑脊液检测显示不明显的寡克隆条带。由于中枢神经系统淋巴瘤不能排除,停止类固醇治疗后进行病变活检。组织学检查排除恶性肿瘤。之后,再次进行核磁共振扫描;它显示了两个新的对比增强病灶。复发-缓解型多发性硬化症(RRMS)的诊断得到确认,并计划使用疾病改善疗法(dmt)进行治疗。结论:MRI上的开环增强很少或没有肿块效应提示肿瘤脱髓鞘病变(TDL)。此外,与中枢神经系统淋巴瘤相比,tdl的相对脑血容量更小,最小和平均表观扩散系数值更高。流式细胞术显示中枢神经系统淋巴瘤为单型B淋巴细胞群,而多发性硬化症无。
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
Acta Medica Lituanica
Acta Medica Lituanica Medicine-General Medicine
CiteScore
0.70
自引率
0.00%
发文量
33
审稿时长
16 weeks
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