Guillain-Barré Syndrome in Older People-A Case Report and Literature Review.

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Xiaomei Chen, Win Ko, Fiza Waseem, Lidia Cilcic, Nahian Kazi, Ahmed Abdelhafiz
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Abstract

Guillain-Barré syndrome (GBS) is the most common acute inflammatory motor polyneuropathy. It affects all age groups, but the incidence increases with increasing age. Before manifesting with neurological symptoms, it is usually preceded by a prodromal phase of infection, most commonly respiratory or gastrointestinal. Pathologically, it is a post-infection immune disorder. The immune response is due to mimicry between the infecting agent and axolemmal surface molecules, which triggers an acute immune injury that leads to blockade of nerve conduction. Age-related decline in immune function plays a role in the increased prevalence and severity of GBS in older people. Typical neurological manifestations are ascending paralysis, areflexia and cranial nerve involvement, but sensory loss is uncommon. In up to 25% of cases, autonomic dysfunction occurs, which includes cardiovascular, sudomotor, gastrointestinal or genitourinary symptoms. The development of autonomic dysfunction in GBS is associated with poor prognosis. We report a case of a 78-year-old man who presented with a predominant autonomic dysfunction that led to a delay in the diagnosis. Because of the multiple morbidities associated with old age, the diagnosis of GBS presentation with autonomic dysfunction, without the typical neurological clinical pattern, may be attributed to the existing comorbidities. Therefore, clinical suspicion and close monitoring with respect to the development of autonomic dysfunction, from the first day of hospital admission, are important. The main diagnostic tests are cerebrospinal fluid analysis looking for protein-cell dissociation and nerve conduction studies to confirm the neuropathy. Treatment involves general supportive care, specific immunological intervention by intravenous immunoglobulins or plasma exchange courses and neurorehabilitation. Severe cases may require intensive care admission and mechanical ventilation. More than 80% of cases will fully recover, but 10% may have residual disability, with mortality estimated at 3-7%. Older age, multiple morbidities, severe weakness, autonomic dysfunction and the need for mechanical ventilation are poor prognostic factors.

老年人格林-巴利综合征1例报告及文献复习。
格林-巴罗综合征(GBS)是最常见的急性炎性运动神经病变。它影响所有年龄组,但发病率随着年龄的增长而增加。在表现为神经系统症状之前,通常先有感染的前驱期,最常见的是呼吸道或胃肠道感染。病理上,它是一种感染后免疫紊乱。免疫反应是由于感染因子和腋膜表面分子之间的模仿,从而引发急性免疫损伤,导致神经传导受阻。与年龄相关的免疫功能下降在老年人GBS患病率和严重程度增加中起作用。典型的神经学表现为上升性麻痹、反射反射和脑神经受累,但感觉丧失并不常见。在高达25%的病例中,发生自主神经功能障碍,包括心血管、性运动、胃肠道或泌尿生殖系统症状。GBS患者发生自主神经功能障碍与预后不良有关。我们报告一例78岁的男性谁提出了主要的自主神经功能障碍,导致延误诊断。由于与老年相关的多种疾病,GBS的诊断表现为自主神经功能障碍,没有典型的神经学临床模式,可能归因于现有的合并症。因此,从入院的第一天起,临床怀疑和密切监测自主神经功能障碍的发展是很重要的。主要的诊断检查是脑脊液分析寻找蛋白质细胞分离和神经传导检查以确认神经病变。治疗包括一般的支持性护理,通过静脉注射免疫球蛋白或血浆交换课程和神经康复进行特异性免疫干预。严重者可能需要重症监护住院和机械通气。80%以上的病例将完全康复,但10%可能留下残废,死亡率估计为3-7%。年龄较大、多种疾病、严重虚弱、自主神经功能障碍和需要机械通气是不良预后因素。
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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来源期刊
CiteScore
0.80
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0.00%
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