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Scleritis Associated with SAPHO Syndrome: A Case Report
Rie Tanaka1, Keiichi Sakurai2, Toshikatsu Kaburaki1
1a Department of Ophthalmology , The University of Tokyo Hospital , Tokyo , Japan.
Ocular Immunology and Inflammation
|January 7, 2017
Summary
A rare case of scleritis, an eye inflammation, was diagnosed in a patient with Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) syndrome. Early recognition of systemic symptoms is crucial for timely diagnosis and treatment.
Area of Science:
- Ophthalmology
- Rheumatology
- Dermatology
Background:
- SAPHO syndrome is a rare autoinflammatory disorder characterized by the simultaneous occurrence of synovitis, acne, pustulosis, hyperostosis, and osteitis.
- Ocular manifestations, such as scleritis, are uncommon in SAPHO syndrome but can be the presenting sign.
Observation:
- A 31-year-old woman presented with bilateral painful red eyes, diagnosed as anterior diffuse scleritis via slit-lamp examination.
- The patient had a prior diagnosis of palmoplantar pustulosis and presented with hyperostosis of the sacroiliac joint and inflammation of sternoclavicular and sternocostal joints.
Findings:
- The patient was diagnosed with SAPHO syndrome after excluding other potential causes.
- This case highlights the infrequent association between scleritis and SAPHO syndrome.
Implications:
- Early identification of systemic symptoms is critical for the prompt diagnosis of SAPHO syndrome.
- Consultation with rheumatologists is essential for accurate diagnosis and management of patients with suspected SAPHO syndrome.
- Ophthalmologists should consider SAPHO syndrome in patients presenting with scleritis, especially those with a history of pustulosis or joint inflammation.
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