ABSTRACT
Purpose: The authors report a38-year-old woman with primary Sjögren’s syndrome who initially showed recurrent blurred vision caused by uveal effusion syndrome and later developed dry mouth, dry eyes, and arthralgia. During the 5-year-course of disease, the patient’s 3-time-onset was all manifested as blurred vision after decreased immunity. Despite the initial absence of sufficient immunological evidence, the final presence of positive serum anti-SS-A, rheumatoid factors, ANA, and inflammatory findings in minor salivary gland biopsy indicated primary Sjögren’s syndrome.
Methods: Retrospective review of a case note.
Conclusions: The manifestation of UES requires further exploration of its real pathogenesis, and the possibility of systemic disease should never be excluded.
Declaration of Interest
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the article.