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吉兰-巴雷综合征作为系统性红斑狼疮的首发表现——病例报告及文献复习

Guillian-Barre syndrome as the initial presentation of systemic lupus erythematosus--case report and review of literature.

作者信息

Nadri Quaid, Althaf Mohammed Mahdi

机构信息

Quaid Johar Nadri, MD, MBC 46 Department of Medicine, King Faisal Specialist Hospital and Research Centre,, PO Box 3354 Riyadh 11211, Saudi Arabia, T: 966-11-442-7492 F: 966-11-442-7499,

出版信息

Ann Saudi Med. 2015 May-Jun;35(3):263-5. doi: 10.5144/0256-4947.2015.263.

Abstract

A number of neurological entities have been associated with systemic lupus erythematosus (SLE). Gullian-Barre syndrome (GBS) as a presenting feature of SLE remains uncommon with just 9 cases reported in the last half-century with the first case reported in 19641-9 (Table 1). We report a young female presenting with GBS in whom SLE and WHO class V lupus nephritis (LN) was subsequently diagnosed. The neurological symptoms partially responded to pulse methylprednisone, intravenous immunoglobulin (IVIG) and plasmapheresis.

摘要

许多神经系统疾病与系统性红斑狼疮(SLE)相关。格林-巴利综合征(GBS)作为SLE的首发特征仍然不常见,在过去半个世纪中仅报告了9例,首例于1964年报告1-9(表1)。我们报告了一名以GBS就诊的年轻女性,随后被诊断为SLE和世界卫生组织V级狼疮性肾炎(LN)。神经症状对脉冲甲基强的松龙、静脉注射免疫球蛋白(IVIG)和血浆置换有部分反应。

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