Tumefactive Multiple Sclerosis: The Lethal Chameleon.

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2024-09-14 eCollection Date: 2024-01-01 DOI:10.12890/2024_004779
Ana Carolina Monteiro, Tomás França de Santana, Carolina Chumbo, Catarina Negrão, Teresa Valido, Filipa Figueiredo, Clara Matos
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引用次数: 0

Abstract

Tumefactive multiple sclerosis (TMS) is a rare variant of multiple sclerosis that presents with a large demyelinating lesion in the central nervous system, accompanied by peripheral ring-like enhancement, perilesional oedema and mass effect. We report a case of a 59-year-old woman who was admitted to the hospital with a four-day history of somnolence, muscle weakness in her left extremities and ultimately, loss of consciousness. Over the following 48 hours, the patient's condition worsened with progressive consciousness impairment. Although the results of the initial head computed tomography (CT) scan supported the diagnosis of a multifocal ischaemic stroke, toxoplasmosis was proposed as the most credible diagnostic hypothesis by brain magnetic resonance imaging (MRI). Due to the adverse clinical progression following the initiation of targeted therapy and inconclusive investigation, a brain biopsy was performed, which was indicative of active TMS in a subacute phase. The patient was started on plasmapheresis and natalizumab along with corticosteroids, with a very good response. In conclusion, we report a biopsy-proven TMS diagnosis in a patient that clinically mimicked an acute stroke and was radiographically confounded with intracranial toxoplasmosis. It highlights that TMS is an uncommon neurological demyelinating disease that is often misdiagnosed. It also emphasises the importance of establishing an accurate differential diagnosis to promptly initiate aggressive immunosuppressive treatment, which may result in a more favourable prognosis.

Learning points: Tumefactive multiple sclerosis is an uncommon variant of multiple sclerosis that presents a substantial diagnostic challenge due to its potential to resemble the clinical and radiological characteristics of other central nervous system (CNS) pathologies, including neoplasms, granulomatous diseases, abscesses and vasculitis.Despite the fact that multimodal imaging studies may help narrow the differential diagnosis, a biopsy is often required to reach a definitive diagnosis and should not be delayed.Awareness of this condition among non-neurologists is critical since a timely and accurate diagnosis prompts aggressive immunomodulatory treatments that may delay a second demyelinating event or progression to clinically definite multiple sclerosis.

肿瘤活性多发性硬化症:致命的变色龙
肿瘤活动性多发性硬化症(TMS)是多发性硬化症的一种罕见变异型,表现为中枢神经系统大面积脱髓鞘病变,伴有外周环状强化、肢端水肿和肿块效应。我们报告了一例 59 岁女性患者的病例,她因 4 天前出现嗜睡、左侧肢体肌无力并最终失去知觉而入院。在随后的 48 小时内,患者病情恶化,意识逐渐受损。虽然最初的头部计算机断层扫描(CT)结果支持多灶性缺血性中风的诊断,但脑磁共振成像(MRI)提出弓形虫病是最可信的诊断假说。由于开始接受靶向治疗后临床进展不佳,且调查尚无定论,因此进行了脑活检,结果显示弓形虫病处于亚急性活动期。患者开始接受血浆置换术和纳他珠单抗以及皮质类固醇治疗,取得了很好的疗效。总之,我们报告了一名患者经活检证实的 TMS 诊断,该患者临床症状类似急性中风,影像学表现与颅内弓形虫病相混淆。报告强调,TMS 是一种不常见的神经系统脱髓鞘疾病,经常被误诊。它还强调了建立准确鉴别诊断的重要性,以便及时启动积极的免疫抑制治疗,这可能会带来更有利的预后:学习要点:肿瘤活动性多发性硬化症是多发性硬化症的一种不常见变异型,由于其可能与其他中枢神经系统(CNS)病变(包括肿瘤、肉芽肿性疾病、脓肿和血管炎)的临床和放射学特征相似,因此给诊断带来了巨大挑战。尽管多模态影像学检查有助于缩小鉴别诊断的范围,但通常需要进行活检才能得出明确诊断,因此不应拖延。非神经病学专家对这种疾病的认识至关重要,因为及时准确的诊断可促使患者接受积极的免疫调节治疗,从而延缓第二次脱髓鞘事件或发展为临床明确的多发性硬化症。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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