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Sjogren’s Disease—Aspects of Clinical Disease Beyond Dry Eyes/Mouth

  • Simon J. Bowman*
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

4 Downloads (Pure)

Abstract

Primary Sjogren’s Disease (SjD) is characterized by features of dryness arising from inflammation in the secretary glands, particularly the salivary and lachrymal glands. Generalized symptoms of fatigue and limb pain are very common but, in addition, about 40% of patients have one or more features of organ-specific systemic disease. This review goes through the background of SjD including diagnosis and classification, epidemiology, impact and investigations such as ultrasound and lip biopsy. It then focuses in detail on each of the systemic organ-specific features, principally using the European League against Rheumatism (EULAR) Sjogren’s Syndrome Disease Activity Index (ESSDAI) along with some non-ESSDAI domains, before concluding with comments on disease heterogeneity, treatment, vaccination, pregnancy and surgery along with observations on patient perspectives. The aim is to provide a general overview of these aspects of the disease to complement other chapters in this monograph.
Original languageEnglish
Article number1189
Number of pages13
JournalJournal of Clinical Medicine
Volume15
Issue number3
DOIs
Publication statusPublished - 2 Feb 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • review
  • Sjogren’s
  • systemic features

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