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MRI阴性的横贯性脊髓炎揭示了一名年轻女性的血清阳性类风湿性关节炎。

MRI-Negative Transverse Myelitis Revealing Seropositive Rheumatoid Arthritis in a Young Woman.

作者信息

Roa Forster Valentina, Castellanos Lisett, Khatib Mohammed, Perez Gabriela

机构信息

Neurology, Herbert Wertheim College of Medicine, Florida International University, Miami, USA.

Neurology, Palmetto General Hospital, Miami, USA.

出版信息

Cureus. 2025 Aug 4;17(8):e89330. doi: 10.7759/cureus.89330. eCollection 2025 Aug.

Abstract

Transverse myelitis (TM) is an inflammatory disorder of the spinal cord often associated with autoimmune diseases, such as systemic lupus erythematosus (SLE) or neuromyelitis optica spectrum disorder (NMOSD); however, it is rarely linked to rheumatoid arthritis (RA). We present the case of a 28-year-old woman with subacute ascending numbness, lancinating pain, and bilateral lower extremity weakness resulting in significant functional impairment. Despite upper motor neuron signs on examination and supportive cerebrospinal fluid findings, including elevated gamma globulins and positive myelin basic protein, spinal MRI remained negative. The patient failed to improve with corticosteroids but showed a significant response to intravenous immunoglobulin. Electrophysiological studies indicated a central process, and serologic workup later revealed rheumatoid factor positivity. She was ultimately diagnosed with seropositive RA and started on certolizumab pegol. Alternative diagnoses, including multiple sclerosis (MS), NMOSD, Guillain-Barré syndrome, and compressive or ischemic myelopathy, were ruled out. This case highlights the diagnostic challenge of MRI-negative TM and its potential association with systemic autoimmune disease, specifically RA. It emphasizes the importance of clinical vigilance, early cerebrospinal fluid analysis, and prompt immunotherapy even in the absence of imaging abnormalities. Our findings broaden the neurologic spectrum of RA and support the role of infection-triggered immune dysregulation in autoimmune myelitis.

摘要

横贯性脊髓炎(TM)是一种脊髓炎性疾病,常与自身免疫性疾病相关,如系统性红斑狼疮(SLE)或视神经脊髓炎谱系障碍(NMOSD);然而,它很少与类风湿关节炎(RA)相关。我们报告一例28岁女性病例,该患者出现亚急性上行性麻木、刺痛和双侧下肢无力,导致严重功能障碍。尽管检查时有上运动神经元体征以及脑脊液检查结果支持诊断,包括γ球蛋白升高和髓鞘碱性蛋白阳性,但脊髓MRI检查结果仍为阴性。患者使用皮质类固醇治疗无效,但对静脉注射免疫球蛋白有显著反应。电生理研究提示为中枢性病变,血清学检查后来显示类风湿因子阳性。她最终被诊断为血清学阳性的RA,并开始使用赛妥珠单抗治疗。排除了其他诊断,包括多发性硬化(MS)、NMOSD、吉兰 - 巴雷综合征以及压迫性或缺血性脊髓病。该病例突出了MRI阴性的TM的诊断挑战及其与全身性自身免疫性疾病,特别是RA的潜在关联。它强调了临床警惕性、早期脑脊液分析以及即使在没有影像学异常的情况下及时进行免疫治疗的重要性。我们的发现拓宽了RA的神经系统疾病谱,并支持感染引发的免疫失调在自身免疫性脊髓炎中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12406755/554a0568b9d3/cureus-0017-00000089330-i01.jpg

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