Systemic lupus erythematosus is easily misdiagnosed as subacute combined degeneration

Hui Zhang, Yitao He, Yi Guo
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Abstract

Background and objective: Systemic lupus erythematosus is likely the cause of neurological dysfunction manifested as subacute combined degeneration. The objective of this article is to report the clinical manifestation of systemic lupus erythematosus manifested as subacute combined degeneration. Methods: We retrospectively analyzed the clinical data of a 37-year-old female patient with systemic lupus erythematosus accompanied by subacute combined degeneration who received treatment at Shenzhen People's Hospital, China. This study met the requirements of the Declaration of Helsinki and the patient gave informed consent. Results: The patient initially presented the symptoms of numbness and weakness of both upper and lower limbs and urinary retention. The patient's physical signs involved peripheral nerve, and posterior and lateral columns of the spinal cord. Blood test revealed anemia and low folate level. Her clinical manifestation was consistent with subacute combined degeneration. But serum antinuclear antibodies (ANA), anti-double-stranded DNA (anti-dsDNA) antibodies, anti-Ro/Sjögren's antibodies (anti-Ro/SSA) and anti-La/Sjögren's antibodies (anti-La/SSB) were found to be positive. Finally, the diagnosis of systemic lupus erythematosus was considered. Conclusion: Systemic lupus erythematosus can cause a variety of neurological defect symptoms, especially in female patients. Tests for autoantibodies should be performed to reduce misdiagnosis rate.
系统性红斑狼疮易误诊为亚急性合并变性
背景和目的:系统性红斑狼疮可能是神经功能障碍的原因,表现为亚急性合并变性。本文旨在报道以亚急性合并变性为表现的系统性红斑狼疮的临床表现。方法:回顾性分析深圳人民医院收治的1例37岁女性系统性红斑狼疮伴亚急性合并变性患者的临床资料。本研究符合《赫尔辛基宣言》的要求,患者给予知情同意。结果:患者最初表现为上肢和下肢麻木无力和尿潴留。患者的体征累及周围神经、脊髓后柱和侧柱。血液检查显示贫血和低叶酸水平。临床表现符合亚急性合并变性。血清抗核抗体(ANA)、抗双链DNA抗体(抗dsdna)、抗ro /Sjögren抗体(抗ro /SSA)和抗la /Sjögren抗体(抗la /SSB)均呈阳性。最后,讨论系统性红斑狼疮的诊断。结论:系统性红斑狼疮可引起多种神经系统缺损症状,尤其是女性患者。应进行自身抗体检测,以减少误诊率。
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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