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Central nervous system compromise in primary Sjogren's syndrome

机译:中枢神经系统损害原发性干燥综合征

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Central nervous system (CNS) involvement in primary Sjogren's syndrome (SS) is poorly understood, and its frequency as well as its manifestations are subjects of controversy. The current study was undertaken to determine the prevalence and the clinical and immunogenetic characteristics of CNS compromise in a well defined group of patients with primary SS. In this retrospective study, patients fulfilled the European classification criteria. Among 120 patients with primary SS, 3 (2.5%) had CNS compromise (multiple sclerosis-like illness, complicated migraine, and optic neuritis with epilepsy). The CNS involvement coincided with the onset of sicca symptoms in 1 case. All 3 patients carried the human leukocyte antigen (HLA) DQB1*0303 allele and tested positive for anti-Ro antibodies, but not for anti-cardiolipin antibodies. Although rare, CNS compromise in primary SS can be the presenting manifestation of the disease in a few cases, and may be severe and varied.
机译:对中枢神经系统(CNS)参与原发性干燥综合征(SS)的了解甚少,其频率及其表现形式也引起争议。目前的研究是为了确定一组明确定义的原发性SS患者的中枢神经系统损害的患病率以及临床和免疫遗传学特征。在这项回顾性研究中,患者符合欧洲分类标准。在120例原发性SS患者中,有3例(2.5%)患有中枢神经系统损害(多发性硬化样疾病,复杂性偏头痛和癫痫性视神经炎)。 1例中枢神经系统受累与干ic症状发作同时发生。所有3例患者均携带人类白细胞抗原(HLA)DQB1 * 0303等位基因,且抗Ro抗体呈阳性反应,但抗心磷脂抗体未呈阳性反应。尽管很少见,CNS在原发性SS中的损害在少数情况下可能是该疾病的表现形式,并且可能很严重且多种多样。

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