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急诊科吉兰-巴雷综合征的临床异质性:对临床结局的影响。

Clinical Heterogeneity of Guillain-Barré Syndrome in the Emergency Department: Impact on Clinical Outcome.

作者信息

Papathanasiou Athanasios, Markakis Ioannis

机构信息

Department of Neurology, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Derby Road, Nottingham NG7 2UH, UK.

Department of Neurology, "St. Panteleimon" General State Hospital, 18454 Nikaia, Greece.

出版信息

Case Rep Emerg Med. 2016;2016:4981274. doi: 10.1155/2016/4981274. Epub 2016 Sep 27.

Abstract

Guillain-Barré syndrome (GBS) is mainly classified into acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axonal neuropathy (AMAN). Although diagnosis of GBS requires progressive weakness and universal areflexia or hyporeflexia, cases of GBS with preserved or increased deep tendon reflexes (DTRs) have been increasingly recognized. We report three cases of GBS, presenting at a single unit in six months. Our first case presented with pure sensory symptoms. The second case had nonspecific generalized weakness, while the third presented with typical ascending weakness. One of our patients had preserved DTRs, while the other two had increased DTRs. Our two cases with hyperreflexia were found to have a preceding infection and anti-ganglioside antibodies, and their electrophysiological studies revealed AMAN. The other case had an AIDP. Only one case was offered a diagnosis and treatment from the first emergency department (ED) visit and had a better clinical outcome. Clinical diagnosis of GBS in the ED can be challenging. Delay in diagnosis of GBS in the ED is common due to cases with intact or increased DTRs, atypical pattern of weakness, or pure sensory symptoms. Emergency physicians should be aware of GBS clinical heterogeneity, because early diagnosis and treatment improve clinical outcome.

摘要

吉兰-巴雷综合征(GBS)主要分为急性炎症性脱髓鞘性多发性神经病(AIDP)和急性运动轴索性神经病(AMAN)。尽管GBS的诊断需要进行性肌无力以及普遍的腱反射消失或减弱,但腱反射保留或增强的GBS病例已越来越多地被认识到。我们报告了6个月内在同一科室出现的3例GBS病例。我们的第一例表现为单纯感觉症状。第二例有非特异性全身肌无力,而第三例表现为典型的上行性肌无力。我们的1例患者腱反射保留,另外2例腱反射增强。我们发现2例腱反射亢进的患者之前有感染及抗神经节苷脂抗体,其电生理研究显示为AMAN。另一例为AIDP。仅1例患者在首次急诊就诊时就得到了诊断和治疗,且临床结局较好。在急诊对GBS进行临床诊断可能具有挑战性。由于存在腱反射正常或增强、肌无力模式不典型或单纯感觉症状的病例,急诊中GBS诊断延迟很常见。急诊医生应了解GBS的临床异质性,因为早期诊断和治疗可改善临床结局。

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