| Title | [In Process Citation] | | Author(s) | Claeys V, Wackens G | | Institution | Service de Stomatologie et de Chirurgie maxillo-faciale, Algemeen Ziekenhuis Oudenaarde, Minderbroedersstraat 3, 9700 Oudenaarde. veerle.claeys@azoudenaarde.be | | Source | Rev Belge Med Dent 2006; 61(3):161-72. | | Abstract | Sjögren syndrome is one of the most prevalent autoimmune diseases in which the body's immune system mistakenly attacks its own moisture producing glands. Although Sjögren syndrome occurs in all age groups in both women and men, women in their fourties are the most affected. Sjögren's syndrome can occur alone or in the presence of another connective tissue disease, respectively called primary and secundary Sjögren syndrome. When two of the three clinical hallmarks: keratoconjunctivitis sicca, xerostomia or connective tissue disease are present, Sjögren 's syndrome should be considered. To confirm the diagnosis of Sjögren's syndrome several tests are required. e.g. blood tests, ophthalmologic tests and oral tests. Rheumatologists have the primary responsibility for managing Sjögren's syndrome. Other specialists can treat the related symptoms. The incidence of lymphoma is higher in patients with Sjögren's syndrome than in the general population. Therefore patients must be monitored carefully for the development of related autoimmune diseases, lymphoma and other complications. Sjögren's syndrome is serious but generally not fatal if complications are diagnosed and treated early. | | Language | fre | | Pub Type(s) | English Abstract
Journal Article
| | PubMed ID | 17408137 |
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