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择期脊柱手术后发生的一种罕见的格林-巴利综合征轴索性变异型

A Rare Axonal Variant of Guillain-Barré Syndrome following Elective Spinal Surgery.

作者信息

Dowling Jessica R, Dowling Thomas J

机构信息

Charles E. Schmidt College of Medicine at Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431, USA.

Long Island Spine Specialists PC, 763 Larkfield Road, Commack NY 11725, USA.

出版信息

Case Rep Orthop. 2018 Aug 7;2018:2384969. doi: 10.1155/2018/2384969. eCollection 2018.

Abstract

Acute motor and sensory axonal neuropathy (AMSAN) is a rare axonal variant of Guillain-Barré syndrome. AMSAN is considered the most severe form of GBS, known for its rapid onset of severe symptoms, and often leading to quadriparesis within 7 days of initial symptom onset. We present a case of a middle-aged Caucasian female who developed AMSAN 2 weeks following an elective spinal surgery. Although rare, GBS has been reported as a complication of surgery. GBS classically presents as ascending motor weakness starting in the lower extremities following a gastrointestinal or upper respiratory tract infection. This patient's GBS manifested slightly differently, with both sensory and motor symptoms of her thoracic region and lower extremities, with no preceding history indicative of infection. To the authors' knowledge, this is the first reported case of AMSAN following spinal surgery. Because of its risk of significant morbidity and mortality, as well as similar presentation to more common spinal postoperative complications, GBS should always be included in the differential diagnosis whenever motor or sensory weakness is observed after spinal surgery.

摘要

急性运动和感觉轴索性神经病(AMSAN)是吉兰-巴雷综合征的一种罕见的轴索性变体。AMSAN被认为是吉兰-巴雷综合征最严重的形式,以严重症状快速起病为特征,且常在初始症状出现后7天内导致四肢瘫。我们报告一例中年白种女性病例,该患者在择期脊柱手术后2周发生了AMSAN。虽然罕见,但吉兰-巴雷综合征已被报道为手术并发症。吉兰-巴雷综合征典型表现为在胃肠道或上呼吸道感染后从下肢开始的上行性运动无力。该患者的吉兰-巴雷综合征表现略有不同,其胸段和下肢出现感觉和运动症状,且无提示感染的既往史。据作者所知,这是首例脊柱手术后发生AMSAN的报道病例。由于其有显著发病和死亡风险,以及与更常见的脊柱术后并发症表现相似,所以每当脊柱手术后观察到运动或感觉无力时,吉兰-巴雷综合征都应始终列入鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a7a/6109579/c78d48404d26/CRIOR2018-2384969.001.jpg

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