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伴有慢性炎症性脱髓鞘性多发性神经根神经病的系统性红斑狼疮患者中抗GM1和GM3神经节苷脂的血清抗体

Serum antibodies to GM1 and GM3-gangliosides in systemic lupus erythematosus with chronic inflammatory demyelinating polyradiculoneuropathy.

作者信息

Sindern E, Stark E, Haas J, Steck A J

机构信息

Department of Neurology and clinical Neurophysiology, Medical School of Hannover, Germany.

出版信息

Acta Neurol Scand. 1991 Jun;83(6):399-402. doi: 10.1111/j.1600-0404.1991.tb03971.x.

Abstract

Acute symmetric demyelinating polyneuropathy of the Guillain-Barré type is known in systemic lupus erythematosus (SLE). Chronic idiopathic demyelinating polyneuropathy (CIDP) has been reported rarely with SLE. A case is reported of CIDP accompanying SLE with autoantibodies against GM1- and GM3-gangliosides. There was no historical evidence to suggest SLE, and CIDP was the first manifestation of SLE. The 38-year-old patient had elevated CSF-protein, slow nerve conduction velocities, sural nerve biopsy revealed mixed axon loss with demyelination and CIDP white matter lesions were observed in magnetic resonance imaging, the GM1- and GM3-autoantibodies may play a role in the pathogenesis of CIDP in SLE.

摘要

格林-巴利型急性对称性脱髓鞘性多发性神经病在系统性红斑狼疮(SLE)中较为常见。慢性特发性脱髓鞘性多发性神经病(CIDP)与SLE相关的报道较为罕见。本文报道了1例伴有抗GM1和GM3神经节苷脂自身抗体的CIDP合并SLE患者。既往无提示SLE的病史证据,CIDP是SLE的首发表现。该38岁患者脑脊液蛋白升高,神经传导速度减慢,腓肠神经活检显示轴突混合性丢失伴脱髓鞘,磁共振成像观察到CIDP白质病变,GM1和GM3自身抗体可能在SLE中CIDP的发病机制中起作用。

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