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伴有接触蛋白相关蛋白2(CASPR2)抗体的艾萨克斯综合征:三例病例系列

Isaacs syndrome with CASPR2 antibody: A series of three cases.

作者信息

Song Jie, Jing Sisi, Quan Chao, Lu Jun, Qiao Xiangyang, Qiao Kai, Lu Jiahong, Xi Jianying, Zhao Chongbo

机构信息

Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.

Department of Electromyography, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

J Clin Neurosci. 2017 Jul;41:63-66. doi: 10.1016/j.jocn.2017.02.063. Epub 2017 Apr 21.

Abstract

Isaacs syndrome is a form of peripheral nerve hyperexcitability, characterized by spontaneous muscle twitching and stiffness. Some patients are reported to be positive for CASPR2 antibody that may be one of the pathogenic autoantibodies in Isaacs syndrome. We reported a series of three patients with Isaacs syndrome, including their clinical features, electrophysiologic findings, laboratory parameters and therapeutic responses. All the three patients were positive for CASPR2 antibodies examined on transfected human embryonic kidney 293 cells by indirect immunofluorescence method. One patient had invasive thymoma. Symptomatic treatment was not sufficient for them, while immunotherapies including corticosteroids, double filtration plasmapheresis and rituximab provided favorable outcomes. The titers of CASPR2 antibody decreased after immune modulating therapy in parallel to clinical improvements in two patients.

摘要

艾萨克斯综合征是一种周围神经兴奋性增高的疾病,其特征为肌肉自发性抽搐和僵硬。据报道,部分患者的接触蛋白相关蛋白2(CASPR2)抗体呈阳性,该抗体可能是艾萨克斯综合征的致病性自身抗体之一。我们报告了一组3例艾萨克斯综合征患者,包括他们的临床特征、电生理检查结果、实验室参数及治疗反应。通过间接免疫荧光法在转染的人胚肾293细胞上检测,所有3例患者的CASPR2抗体均呈阳性。其中1例患者患有侵袭性胸腺瘤。对症治疗对他们并不充分,而包括皮质类固醇、双重滤过血浆置换和利妥昔单抗在内的免疫疗法取得了良好疗效。在2例患者中,免疫调节治疗后CASPR2抗体滴度下降,同时临床症状改善。

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