Sjogren's syndrome

Last edited 02/2021 and last reviewed 07/2023

Primary Sjogren's syndrome is the association of

  • keratoconjunctivitis sicca and/or xerostomia, with
  • rheumatoid arthritis or other connective tissue disorder

Sicca refers to dryness most often involving the eyes and mouth due to inflammation and resultant pathology of the lacrimal and salivary glands.

Salivary gland biopsy shows sialadenitis. Involvement of other secretory glands is common causing dyspareunia, dry skin, dysphagia, otitis media and pulmonary infection.

Up to one-half of affected individuals also develop extra-glandular involvement implying the occurrence of signs and symptoms in organs distinct from the salivary and lacrimal glands including the joints, skin, lungs, gastrointestinal (GI) tract, nervous system, and kidney

Other possible features include dental caries, attacks of monilial stomatitis, neuropathy, hepatosplenomegaly and renal involvement.

Associations include renal tubular acidosis, adverse drug reactions and lymphoma.

Secondary Sjogren syndrome frequently occurs in conjunction with other autoimmune disorders including rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE)

  • study evidence suggests that secondary Sjogren's syndrome in rheumatoid arthritis occurs in 17-31% of patients (1,2); although it has been stated that secondary Sjogren's syndrome affects 50% of patients with rheumatoid arthritis (3)

Aetiology of Sjogren syndrome is unknown

  • a genetic predisposition involving the major histocompatibility (MHC) locus is seen
    • association with HLA-B8, HLA-DR3, HLA-DRW52

Reference:

Related pages:

pathology

epidemiology

secondary causes

clinical features

investigations

management of Sjogren's syndrome

prognosis