癫痫持续状态与神经梅毒:1例报告及叙述回顾

IF 1.6 Q3 CLINICAL NEUROLOGY
NeuroSci Pub Date : 2021-12-01 DOI:10.3390/neurosci2040031
G. Giovannini, S. Meletti
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引用次数: 0

摘要

神经梅毒是一种罕见但危及生命的梅毒并发症,它可以在初次感染后几十年发展,并且可能无法识别。癫痫发作和癫痫持续状态(SE)可能是先前未确诊的梅毒患者的第一表现。我们提出了一个由神经梅毒引起的新发作的难治性癫痫持续状态的例子病例,并回顾了现有的文献。我们选择了所有报道SE病例的研究,这些病例既包括已知梅毒诊断的患者,也包括神经梅毒的首次表现。我们确定了50例患者,主要由免疫功能正常的中年男性组成。39例(83%)出现新发SE。经常观察到细微和快速进展的情绪和/或认知障碍病史,提示边缘脑炎样表现。26例报告了局灶性额叶或颞叶SE。脑MRI频繁显示T2/FLAIR高信号广泛累及内侧颞叶和额叶。本综述应提高临床医生对神经梅毒作为不明病因新发SE的可能病因的认识,特别是在“边缘脑炎”样临床表现的背景下。及时发现和治疗神经梅毒可部分或完全逆转神经系统后遗症,改变疾病的自然史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Status Epilepticus and Neurosyphilis: A Case Report and a Narrative Review
Neurosyphilis is a rare but life-threatening complication of syphilis that can develop even decades after the primary infection and can be unrecognized. Seizures and status epilepticus (SE) may represent the first manifestation in a previously undiagnosed syphilitic patient. We present an exemplification case of a new onset refractory status epilepticus caused by neurosyphilis and we reviewed the existing literature. We selected all studies reporting cases of SE in the context both of patients with a known diagnosis of syphilis and as the first manifestation of neurosyphilis. We identified 50 patients, mostly composed of immunocompetent, middle-aged males. Thirty-nine patients (83%) presented a new onset SE. A history of subtle and rapidly progressive mood and/or cognitive impairment suggesting a limbic encephalitis-like presentation was frequently observed. Focal frontal or temporal SE was reported in 26. Brain MRI frequently showed T2/FLAIR hyperintensities widely involving the medial temporal structures and the frontal lobes. This review should increase the clinician’s awareness of neurosyphilis as a possible etiology of a new onset SE of unknown etiology, especially in the context of a “limbic encephalitis”-like clinical presentation. Prompt recognition and treatment for neurosyphilis partially or completely reverse neurologic sequelae, changing the natural history of the disease.
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