神经梅毒致吉兰-巴雷综合征 1 例报告
Neurosyphilis presenting with Guillain-Barre syndrome: a case report.
机构信息
Department of Neurosciences, University of California San Diego, San Diego, California, USA.
出版信息
BMC Neurol. 2023 Nov 25;23(1):421. doi: 10.1186/s12883-023-03471-5.
BACKGROUND
Syphilis is associated with a wide variety of systemic presentations, earning it the moniker "The great mimicker". Neurosyphilis is classically associated with meningovasculitis in the acute-subacute stage and tabes dorsalis and dementia paralytica in later stages. However, one of the less well described presentations include Guillain-Barre Syndrome. This case presents a patient with an ascending polyneuropathy suspicious for Guillain-Barre Syndrome who also had other atypical findings including a truncal sensory loss, optic disc swelling, and rash ultimately found to have neurosyphilis. Electrodiagnostic testing was consistent with demyelination, supporting a diagnosis of neurosyphilis associated Guillain-Barre Syndrome.
CASE PRESENTATION
A 37-year-old female presented to the emergency department with a weakness and difficulty swallowing. She described a three-month history of symptoms, initially starting with a persistent headache followed by one month of a pruritic rash on her chest, palms, and soles. Two weeks prior to presentation, she developed progressive weakness in her arms, numbness in her arms and chest, and difficulty swallowing. Neurological exam was notable for multiple cranial neuropathies, distal predominant weakness in all extremities, length-dependent sensory loss, and hyporeflexia. Investigation revealed a positive Venereal Disease Research Laboratory in her cerebrospinal fluid without significant pleocytosis, contrast enhancement in cranial nerves V, VII, and VIII on MRI, and a demyelinating polyneuropathy on electrodiagnostic testing. She was diagnosed with Guillain-Barre syndrome, secondary to neurosyphilis. The patient acutely declined and required intubation, and ultimately made a full recovery after treatment with plasmapheresis and penicillin.
CONCLUSIONS
This case describes a clinical entity of syphilitic Guillain-Barre Syndrome and highlights the importance of including syphilis in the differential of any patient presenting with ascending polyradiculopathy, especially given the resurgence of syphilis.
背景
梅毒可引起多种全身表现,因此被称为“伟大的模仿者”。神经梅毒在急性-亚急性阶段常与脑膜血管炎有关,而在后期则与脊髓痨和麻痹性痴呆有关。然而,其表现之一是不太容易描述的,包括格林-巴利综合征。本病例介绍了一例疑似格林-巴利综合征的进行性多发性神经病患者,该患者还存在其他不典型表现,包括躯干感觉丧失、视盘肿胀和皮疹,最终被发现患有神经梅毒。电诊断检查符合脱髓鞘,支持神经梅毒相关格林-巴利综合征的诊断。
病例介绍
一名 37 岁女性因乏力和吞咽困难到急诊科就诊。她描述了三个月的症状病史,最初是持续性头痛,随后一个月出现胸部、手掌和脚底瘙痒性皮疹。在出现症状前两周,她出现手臂进行性无力、手臂和胸部麻木以及吞咽困难。神经系统检查发现有多处颅神经病变,四肢远端为主的无力,长度依赖性感觉丧失和反射减弱。检查发现脑脊液性病研究实验室阳性,无明显白细胞增多,MRI 显示颅神经 V、VII 和 VIII 增强,电诊断检查显示脱髓鞘多发性神经病。她被诊断为神经梅毒继发的格林-巴利综合征。患者病情迅速恶化,需要插管,经血浆置换和青霉素治疗后完全康复。
结论
本病例描述了一种梅毒性格林-巴利综合征的临床实体,并强调了在任何出现进行性多发性神经病的患者中,包括梅毒在内的鉴别诊断的重要性,特别是鉴于梅毒的重新出现。