Conclusions
SS is a common disorder with significant morbidity that may involve multiple glandular and extraglandular sites with variable severity. A small but significant number of patients (5%) may eventually develop malignant lymphoma. In addition, some aspects of the syndrome are frequently encountered in patients with other autoimmune disorders. This multi-faceted presentation of the disorder demands refined measures for diagnosis and management.
The management of SS patients requires the co-operation of multiple medical disciplines and aims at alleviating symptoms and recognizing and treating complications. Despite significant progress in the understanding of the pathogenesis of SS, treatment of the syndrome remains empirical and symptomatic.
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Moutsopoulos, N.M., Moutsopoulos, H.M. Therapy of Sjögren’s syndrome. Springer Semin Immunopathol 23, 131–145 (2001). https://doi.org/10.1007/s002810100070
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DOI: https://doi.org/10.1007/s002810100070