Department of Neurology, St. Stephen's Hospital, Delhi, 110054, India.
Department of Rheumatology, St. Stephen's Hospital, Delhi, 110054, India.
Rheumatol Int. 2021 Oct;41(10):1855-1866. doi: 10.1007/s00296-020-04716-z. Epub 2020 Oct 11.
Aseptic meningoencephalitis (AME) constitutes a variable proportion of meningoencephalitis. Patients with AME are not routinely evaluated for autoimmune disorders. Primary Sjögren's syndrome (pSS) is a prevalent, but under suspected systemic autoimmune disease characterised by exocrinopathy, though sicca symptoms may not be the dominant or presenting feature. This study was undertaken to enumerate the clinical, radiological and laboratory features of meningoencephalitis related to pSS among the total cohort of meningoencephalitis admitted in our hospital. Retrospective patient records were screened for diagnosis of meningoencephalitis from April 2016 to March 2020. Those patients with anti-SSA positivity and clinical diagnosis of pSS were included. We have reviewed all cases of Sjögren's syndrome with meningoencephalitis available in literature. Four patients with meningoencephalitis with pSS were identified. Their clinical presentations, investigations, and good response to steroids have been described with special emphasis on evolving clinical features. In all patients, sicca features were absent. Anti-SSA was positive in all. The diagnosis of pSS was considered after ruling out all infectious and other autoimmune aetiologies. Two had extra-neurological organ manifestations and required addition of second line immunosuppressive agents for optimum disease control. Consistent with this case series, absent sicca symptoms have been described in pSS patients presenting with meningoencephalitis in literature. This case series is of special interest as it describes the initial presentation of pSS as meningoencephalitis with sicca features in absentia, thereby highlighting the need for a high index of suspicion and the need for workup for pSS in AME.
无菌性脑膜脑炎(AME)构成了脑膜脑炎的一个可变比例。AME 患者通常不会接受自身免疫性疾病的评估。原发性干燥综合征(pSS)是一种普遍存在但易被怀疑的系统性自身免疫性疾病,其特征为外分泌腺病变,尽管干燥症状可能不是主要或表现特征。本研究旨在列举在我院收治的脑膜脑炎总队列中与 pSS 相关的脑膜脑炎的临床、放射学和实验室特征。从 2016 年 4 月至 2020 年 3 月,回顾性筛选患者记录以诊断脑膜脑炎。那些抗 SSA 阳性且临床诊断为 pSS 的患者被纳入研究。我们已经回顾了文献中所有伴有脑膜脑炎的干燥综合征病例。确定了 4 例伴有 pSS 的脑膜脑炎患者。描述了他们的临床表现、检查结果和对类固醇的良好反应,并特别强调了不断演变的临床特征。在所有患者中,均无干燥症状。所有患者抗 SSA 均为阳性。在排除所有感染性和其他自身免疫性病因后,考虑诊断为 pSS。有 2 例患者有神经外器官表现,需要添加二线免疫抑制剂以实现最佳疾病控制。与该病例系列一致,文献中描述了伴有脑膜脑炎的 pSS 患者缺乏干燥症状。该病例系列特别有趣,因为它描述了 pSS 作为脑膜脑炎的初始表现,且无干燥症状,从而强调了对 AME 中 pSS 进行高度怀疑和检查的必要性。