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一名患有系统性红斑狼疮的17岁女性出现复杂运动障碍:可能与抗核糖体P抗体有关。

A 17-year-old female with systemic lupus presents with complex movement disorder: possible relationship with antiribosomal p antibodies.

作者信息

Ozcan Muhammed Emin, Altınöz Meriç Adil, Karadeli Hasan Hüseyin, Asil Talip, Koçer Abdulkadir

机构信息

Department of Neurology, Bezmialem Vakıf University, Adnan Menderes Bulvarı, Vatan Caddesi, 34093 Fatih İstanbul, İstanbul, Turkey.

出版信息

Case Rep Neurol Med. 2013;2013:590729. doi: 10.1155/2013/590729. Epub 2013 May 8.

Abstract

Complex movement disorder is a relatively rare presentation of neurolupus. Antiphospholipid antibodies are associated with movement disorders likely via aberrant neuronal stimulation. Antiribosomal P antibodies have been previously associated with neuropsychiatric disorders but their correlation with movement disorder was not previously established. Our case report involves a 17-year-old Caucasian female patient positive for only antiribosomal P antibody and lupus anticoagulant who presented with a sudden onset of complex movement disorder. After complete cessation of physical signs with olanzapine, anticardiolipin and anti- β 2 glycoprotein I antibodies became positive which indicates a likely discordance between movement disorder and antiphospholipid antibodies. This also indicates a potential causal role of antiribosomal P antibodies in inducing movement disorder.

摘要

复杂运动障碍是神经狼疮相对罕见的一种表现形式。抗磷脂抗体可能通过异常的神经元刺激与运动障碍相关。抗核糖体P抗体此前已与神经精神疾病相关,但它们与运动障碍的相关性此前尚未确立。我们的病例报告涉及一名17岁的白种女性患者,她仅抗核糖体P抗体和狼疮抗凝物呈阳性,表现为突然发作的复杂运动障碍。在使用奥氮平后体征完全消失后,抗心磷脂抗体和抗β2糖蛋白I抗体转为阳性,这表明运动障碍与抗磷脂抗体之间可能存在不一致。这也表明抗核糖体P抗体在诱发运动障碍中可能起因果作用。

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