Guillain - Barre syndrome as the first presentation in a patient with systemic lupus erythromatous; case report

Z. Taha, Shaima N. Elgenaid, M. Ahmed
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引用次数: 1

Abstract

Systemic Lupus Erythromatous (SLE) is an auto immune disease characterized by multi-organ affection, Guillain–Barre syndrome (GBS) is considered as an unusual and one of the least neuropsychiatric syndromes in SLE, this case report aiming to report a rare association of GBS as an initial presentation for an SLE in a female patient. A middle age female was presented with palpitation, shortness of breath and body weakness, she was admitted for four days and diagnosed with atypical GBS. She received Intravenous immunoglobulin (IVIG) for three days but no improvement was been noticed. The patient complained of dry cough, shortness of breath, palpitations and generalized weakness in association with back pain and paraesthesia of the fingers. General examination and lab workup were done and revealed a presence of SLE in relation to GBS. IVIG was then commenced 0.4 g/kg body/weight/day with Hydroxychloroquine 200mg tabs BID, Prednisolone 40mg, calcicare and Mycophenolatemofetil. Significant improvement was noted after receiving the above-mentioned medications and over a period of three months all her symptoms and complains were subside.
系统性红斑狼疮患者首次出现格林-巴利综合征;病例报告
系统性红斑狼疮(SLE)是一种以多器官影响为特征的自身免疫性疾病,格林-巴利综合征(GBS)被认为是SLE中罕见的神经精神综合征之一,本病例报告旨在报告一名女性SLE患者以GBS为首发症状的罕见关联。一名中年女性以心悸、呼吸急促和身体虚弱为表现,入院4天,诊断为非典型GBS。她接受静脉注射免疫球蛋白(IVIG)三天,但没有发现任何改善。患者主诉干咳、呼吸短促、心悸和全身无力,并伴有背痛和手指感觉异常。一般检查和实验室检查显示SLE与GBS相关。然后开始IVIG 0.4 g/kg体重/天,羟氯喹200mg片剂BID,强的松龙40mg,钙钙和霉酚酸酯。在接受上述药物治疗后,她的病情有了明显改善,三个月后,她的所有症状和抱怨都消失了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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