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SLE合并周围神经病少见,在日本,欧美国家不超过10%,合并GBS样多发性神经根炎者罕见。作者报告1例SLE 伴急性起病,在约1个月的期间内症状仍进展的多发性神经根炎,并进行了多次电生理学检查和病理学研究。患者为32岁女性,以双上肢近端无力,继之出现下肢及面肌进行性无力于4月6日入院。既往有多发性关节痛。一般理学检查无异常,双侧周围性面神经瘫,轻度吞咽困难,四肢近端肌力减弱。尤以双上肢为著,腱反射消失,无病理反射,双足感觉迟纯,
SLE rare combination of peripheral neuropathy in Japan, Europe and the United States less than 10%, merger GBS-like multiple nerve root inflammation is rare. The authors report a case of multiple radiculopathies with an acute onset of SLE with symptom progression over a period of about 1 month and a number of electrophysiological and pathological studies. The patient, a 32-year-old female, presented with weakness in his proximal upper extremity followed by progressive weakness of the lower extremities and facial muscles on April 6. Past multiple joint pain. No abnormalities in the general science examination, bilateral peripheral facial paralysis, mild dysphagia, muscle weakness in the proximal extremities. Especially for the upper extremities, tendon reflex disappears, no pathological reflex, feet feel pure,