以格林-巴利综合征为首发表现的系统性红斑狼疮1例

Z. Saremi, Mahdi Bakhshi Mohammadi, Zahra Ahmadi
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种具有不同临床表现的慢性自身免疫性疾病。在罕见的SLE病例中有急性[类似格林-巴勒综合征(GBS)]或慢性(慢性炎性脱髓鞘性多根神经病变)炎性多根神经病变的报道。病例介绍:我们报告了一位39岁的女性,她表现为急性周围神经病变,最终被诊断为SLE。她出现远端麻木和感觉异常,随后进行性上肢和下肢无力,吞咽和说话困难。她在出现症状前三周有类似流感的病史。结论:进行性上肢和下肢无力伴反射屈曲和电诊断提示格林-巴-罗综合征的诊断。一个多月后,患者的神经功能显著恢复,功能持续恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Guillain-Barré Syndrome as the First Presentation of Systemic Lupus Erythematosus
Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with different clinical manifestations. Acute [resembling Guillain-Barré syndrome (GBS)] or chronic (chronic inflammatory demyelinating polyradiculoneuropathy) inflammatory polyradiculoneuropathy has been reported in rare SLE cases. Case Presentation: We reported a 39-year-old woman that presented with acute peripheral neuropathy, and she was eventually diagnosed with SLE. She developed distal numbness and paraesthesia followed by progressive upper and lower extremity weakness and difficulty in swallowing and speaking. She had a history of flu-like illness three weeks before to symptoms. Conclusions: Progressive upper and lower extremity weakness along with areflexia and electrodiagnostic findings suggested the diagnosis of Guillain-Barré syndrome. Over a month, significant neurological recovery occurred, and the patient's function continued to recover.
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