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老年人吉兰-巴雷综合征——病例报告及文献综述

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

作者信息

Chen Xiaomei, Ko Win, Waseem Fiza, Cilcic Lidia, Kazi Nahian, Abdelhafiz Ahmed

机构信息

Department of Geriatric Medicine, Rotherham General Hospital, Moorgate Road, Rotherham S60 2UD, UK.

出版信息

Diseases. 2025 Sep 18;13(9):306. doi: 10.3390/diseases13090306.

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.

摘要

吉兰-巴雷综合征(GBS)是最常见的急性炎性运动性多发性神经病。它影响所有年龄组,但发病率随年龄增长而增加。在出现神经症状之前,通常有一个前驱感染期,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与轴突膜表面分子之间的分子模拟,触发急性免疫损伤,导致神经传导阻滞。免疫功能的年龄相关性下降在老年人GBS患病率和严重程度增加中起作用。典型的神经表现为上行性麻痹、腱反射消失和脑神经受累,但感觉丧失不常见。高达25%的病例会出现自主神经功能障碍,包括心血管、汗腺运动、胃肠道或泌尿生殖系统症状。GBS中自主神经功能障碍的发生与预后不良有关。我们报告一例78岁男性,以主要的自主神经功能障碍为表现,导致诊断延迟。由于与老年相关的多种疾病,GBS以自主神经功能障碍为表现且无典型神经临床模式时,诊断可能归因于现有的合并症。因此,从入院第一天起对自主神经功能障碍的发展进行临床怀疑和密切监测很重要。主要诊断检查是脑脊液分析以寻找蛋白-细胞分离,以及神经传导研究以确认神经病变。治疗包括一般支持治疗、静脉注射免疫球蛋白或血浆置换疗程的特异性免疫干预以及神经康复。严重病例可能需要入住重症监护病房并进行机械通气。超过80%的病例将完全康复,但10%可能有残留残疾,死亡率估计为3-7%。老年、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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cbc/12468067/e056423a5472/diseases-13-00306-g001.jpg

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