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Author Spotlight: Anterior HR-OCT as a Non-Invasive Tool for Characterizing Ocular Surface Squamous Neoplasia
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Ocular involvement in tumoral calcinosis
Harsha Bhattacharjee1, Kasturi Bhattacharjee, Dina Kumar Yambem
1Department of Comprehensive Ophthalmology, Sri Sankaradeva Nethralaya, Guwahati, Assam, India.
Indian Journal of Ophthalmology
|September 19, 2014
Summary
A rare case of vision loss in a 32-year-old male revealed calcific deposits in the eye. This finding was linked to migratory joint swelling and suppuration, indicating a systemic connection.
Area of Science:
- Ophthalmology
- Rheumatology
- Medical Imaging
Background:
- A 32-year-old male presented with a 1.5-year history of progressive blurred vision in his right eye.
- The patient reported migratory swelling over large joints, some resolving after chalky white discharge, with persistent swelling in the gluteal region.
Observation:
- Ophthalmological examination showed severely reduced visual acuity (counting fingers at 1 meter) in the right eye.
- Perilimbal conjunctival calcific deposits and retinal angioid streaks were noted in both eyes.
- Fundus fluorescein angiography (FFA) and optical coherence tomography (OCT) confirmed a choroidal neovascular membrane with subretinal hemorrhage in the right eye.
Findings:
- B scan ultrasonography and vector A scan revealed calcification of the subretinal neovascular membrane.
- Calcification extended to the adjoining sclera, suggesting a widespread calcification process.
- The ocular findings were associated with a history of systemic inflammatory and suppurative joint disease.
Implications:
- This case highlights a potential link between systemic calcific deposition, possibly related to inflammatory arthropathy, and ocular complications like choroidal neovascularization.
- Early detection and comprehensive imaging are crucial for diagnosing and managing such rare conditions.
- Further research is warranted to understand the pathogenesis of this systemic-ocular calcification syndrome.
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