Abstract
Sjögren’s syndrome (SS) is a chronic autoimmune condition characterized by diminished lacrimal and salivary gland function with associated lymphocytic infiltrates of the affected glands. SS may occur in a primary form when it is not associated with other autoimmune disorders or in a secondary form when it complicates another underlying rheumatic disease. Among others, rheumatoid arthritis and systemic lupus erythematosus are the most common diseases associated with SS.
Reduced exocrine gland function is the main pathogenic mechanism underlying the principal clinical manifestations of SS, such as a combination of dry eyes (keratoconjunctivitis sicca) and dry mouth (xerostomia). Salivary gland enlargement is common and occurs in 30–50 % of patients with SS at some point during the course of the disease.
This chapter will focus on parotid and submandibular involvement in Sjögren’s syndrome.
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Sciascia, S., De Marchi, A., Roccatello, D. (2016). Parotid and Submandibular Involvement in Sjögren’s Syndrome. In: Roccatello, D., Emmi, L. (eds) Connective Tissue Disease. Rare Diseases of the Immune System. Springer, Cham. https://doi.org/10.1007/978-3-319-24535-5_22
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