{"title":"复发性无菌性脑膜炎作为原发性Sjögren综合征的初始临床表现","authors":"D. H. Lee, S. Lee","doi":"10.18700/JNC.190077","DOIUrl":null,"url":null,"abstract":"Sjögren’s syndrome (SjS) is a chronic autoimmune disease that may be primary or secondary to other connective tissue disorders, particularly rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. SjS is clinically characterized by sicca symptoms, which develop due to a mononuclear infiltration and secondary chronic dysfunction of the lacrimal and salivary glands. Systemic, extra-glandular manifestations are found in many patients with primary SjS and may occur in almost any organ, including the nervous system. The central nervous system CASE REPORT","PeriodicalId":33246,"journal":{"name":"Journal of Neurocritical Care","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Recurrent aseptic meningitis as an initial clinical presentation of primary Sjögren’s syndrome\",\"authors\":\"D. H. Lee, S. Lee\",\"doi\":\"10.18700/JNC.190077\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sjögren’s syndrome (SjS) is a chronic autoimmune disease that may be primary or secondary to other connective tissue disorders, particularly rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. SjS is clinically characterized by sicca symptoms, which develop due to a mononuclear infiltration and secondary chronic dysfunction of the lacrimal and salivary glands. Systemic, extra-glandular manifestations are found in many patients with primary SjS and may occur in almost any organ, including the nervous system. The central nervous system CASE REPORT\",\"PeriodicalId\":33246,\"journal\":{\"name\":\"Journal of Neurocritical Care\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurocritical Care\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18700/JNC.190077\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Nursing\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurocritical Care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18700/JNC.190077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Nursing","Score":null,"Total":0}
Recurrent aseptic meningitis as an initial clinical presentation of primary Sjögren’s syndrome
Sjögren’s syndrome (SjS) is a chronic autoimmune disease that may be primary or secondary to other connective tissue disorders, particularly rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. SjS is clinically characterized by sicca symptoms, which develop due to a mononuclear infiltration and secondary chronic dysfunction of the lacrimal and salivary glands. Systemic, extra-glandular manifestations are found in many patients with primary SjS and may occur in almost any organ, including the nervous system. The central nervous system CASE REPORT