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Coats Disease With Macular Nodule
Anasua Ganguly Kapoor1, Sameera Nayak2, Simranjeet Aulakh3
1Hima Bindu Yalamanchili Centre for Eye Cancer, L.V. Prasad Eye Institute, Vijayawada.
Insights
Coats disease can present with a macular nodule, a rare variant that mimics retinoblastoma. Early recognition of this lipid accumulation is crucial for accurate diagnosis and treatment.
Area of Science:
- Ophthalmology
- Retinal Diseases
- Pediatric Ophthalmology
Background:
- Coats disease is a rare condition characterized by retinal telangiectasias and exudation.
- Macular involvement in Coats disease can lead to significant vision impairment.
- Distinguishing Coats disease from other intraocular pathologies is critical for appropriate management.
Purpose of the Study:
- To describe a case series of Coats disease presenting with a macular nodule.
- To highlight the potential of this presentation to mimic retinoblastoma.
- To emphasize the importance of recognizing this rare variant for accurate diagnosis and treatment.
Main Methods:
- Retrospective case series analysis.
- Inclusion of patients with Coats disease and macular nodules.
- Review of clinical presentation, imaging (OCT, USG, FFA), and treatment outcomes.
Main Results:
- Seven patients (2%) with Coats disease and macular nodules were identified, all initially diagnosed as retinoblastoma.
- Macular nodules were typically grayish-white, dome-shaped or bilobed, involving the fovea with surrounding exudates.
- Imaging revealed subretinal nodules with posterior shadowing (OCT) and echodense intraocular nodules (USG), with characteristic fluorescein angiography findings.
Conclusions:
- Macular nodules in Coats disease represent focal lipid accumulation within the macula.
- This rare presentation can closely mimic retinoblastoma, necessitating careful evaluation.
- Awareness of this Coats disease variant is essential for appropriate diagnosis and timely intervention to preserve vision.
Purpose:
To describe a case series of Coats disease with macular nodule mimicking retinoblastoma.
Methods:
Retrospective case series.
Results:
Of 339 patients with Coats disease, 7 (2%) with macular nodules were included. All had a referral diagnosis of retinoblastoma. All were males (mean age-6 y). The most common presenting complaint was decreased vision (n=4, 57%). Median best corrected visual acuity at presentation was counting fingers close to face, which was maintained at last follow-up (mean, 8 months). The nodule had a mean diameter of 5x4x3 mm, was grayish white, and bilobed (n=3, 43%), or dome shaped (n=4, 57%) with surface pigmentation (n=4, 57%), involving fovea (n=5, 71%), with surrounding exudates and second- or third-order retinal vessels. OCT (n=4) showed a well-defined hyperreflective subretinal nodule with posterior shadowing, cysts, and exudates. USG (n=6) showed an echodense intraocular nodule with moderate internal reflectivity with hyperechoic foci in 2 (33%) cases. FFA showed early- and mid-phase hypo-fluorescence with focal leakage with late-phase hyperfluorescence. Focal green laser photocoagulation of the telangiectatic vessels was performed in 5, one underwent subretinal fluid drainage and scleral buckling, and one was observed.
Conclusion:
Macular nodule in Coats disease represents a preferential accumulation of lipid in the macula. This rare variant of Coats disease can mimic retinoblastoma process. Be aware of this entity to ensure appropriate diagnosis and treatment.
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