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Vasculitis in primary Sjögren’s syndrome

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The Vasculitides

Abstract

Sjögren’s syndrome (SS) is a chronic autoimmune disease, characterized by lymphocytic infiltration of the exocrine glands resulting in xerostomia and keratoconjunctivitis sicca. These manifestations can occur al.one (primary SS) or in association with other autoimmune disorders, such as rheumatoid arthritis or systemic lupus erythematosus (secondary SS). Extraglandular manifestations are seen in approximately half of SS patients and include Raynaud’s phenomenon, splenomegaly, lymphad-enopathy, lung involvement, kidney involvement, liver involvement and vasculitis [1].

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© 1996 Springer Science+Business Media Dordrecht

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Tzioufas, A.G., Skopouli, F.N., Boumba, D., Moutsopoulos, H.M. (1996). Vasculitis in primary Sjögren’s syndrome. In: Ansell, B.M., Bacon, P.A., Lie, J.T., Yazici, H. (eds) The Vasculitides. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-2889-4_19

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  • DOI: https://doi.org/10.1007/978-1-4899-2889-4_19

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-412-64140-4

  • Online ISBN: 978-1-4899-2889-4

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