Nadri Quaid, Althaf Mohammed Mahdi
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,
Ann Saudi Med. 2015 May-Jun;35(3):263-5. doi: 10.5144/0256-4947.2015.263.
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.
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。
