Department of Neurology, 970th Hospital of PLA Joint Logistic Support Force, Yantai, China.
Front Immunol. 2024 Sep 5;15:1453264. doi: 10.3389/fimmu.2024.1453264. eCollection 2024.
We present an analysis of a case initially manifesting as bilateral horizontal gaze palsy, eventually diagnosed as multiple sclerosis (MS) with preclinical systemic lupus erythematosus (p-SLE). The patient, a 25-year-old male, exhibited restricted movement in both eyes. Cranial MRI revealed multiple demyelinating lesions; serum analyses indicated elevated levels of antinuclear antibodies (ANA), anti-Sm antibodies, and anti-nRNP antibodies. Oligoclonal bands were identified in the cerebrospinal fluid. Neurophysiological assessments demonstrated damage to the optic, auditory, and facial nerves. Given the clinical presentation, laboratory findings, and the progression of the disease, the final diagnosis was confirmed as MS associated with p-SLE. The onset of MS with oculomotor disturbances is rare and may be easily confused with neuropsychiatric systemic lupus erythematosus (NPSLE). Furthermore, the differentiation of p-SLE from undifferentiated connective tissue disease (UCTD) in the early stages presents significant challenges. Early identification of risk factors and close monitoring of disease activity is crucial for an accurate diagnosis.
我们分析了一例最初表现为双侧水平眼球运动障碍的病例,最终诊断为伴有临床前系统性红斑狼疮(p-SLE)的多发性硬化症(MS)。患者为 25 岁男性,表现为双眼运动受限。头颅 MRI 显示多发性脱髓鞘病变;血清分析提示抗核抗体(ANA)、抗 Sm 抗体和抗 nRNP 抗体水平升高。脑脊液中存在寡克隆带。神经生理学评估显示视神经、听神经和面神经受损。鉴于临床表现、实验室结果和疾病进展,最终诊断为 MS 伴 p-SLE。伴有眼动障碍的 MS 发作较为罕见,可能容易与神经精神系统性红斑狼疮(NPSLE)混淆。此外,在早期阶段区分 p-SLE 与未分化结缔组织病(UCTD)具有很大挑战性。早期识别风险因素并密切监测疾病活动对于准确诊断至关重要。