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Atypical Presentation of Choroidal Osteoma: Two Case Reports
Dafne Fernandes Machado1, Stela Souza Peña1, Mariana Carneiro Alves1
1Ophthalmology Discipline, Centro Universitário Saúde ABC/ Faculdade de Medicina Do ABC, Santo André, Brasil.
International Medical Case Reports Journal
|November 6, 2024
Summary
Choroidal osteoma, a rare benign tumor, can be misdiagnosed. This report details two cases, highlighting the importance of multimodal evaluation for accurate diagnosis and management of this vision-threatening condition.
Area of Science:
- Ophthalmology
- Oncology
Background:
- Choroidal osteoma is a rare, benign osseous choristoma.
- It typically presents unilaterally, favoring females and juxtapapillary locations.
- Visual loss occurs in nearly 60% of affected eyes, often when the macula is involved.
Observation:
- Two distinct cases of choroidal osteoma are presented.
- Case 1: A 74-year-old male with blurred vision, initially misdiagnosed as age-related macular degeneration.
- Case 2: A 19-year-old female with a history of choroidal hemangioma, presenting with blurred vision and macular detachment.
Findings:
- Accurate diagnosis of choroidal osteoma can be challenging due to its varied presentation.
- Multimodal imaging is crucial for differentiating choroidal osteoma from other fundus lesions.
- Successful diagnosis was achieved after cataract surgery in the first case and through examination in the second.
Implications:
- Early and accurate diagnosis of choroidal osteoma is vital for timely intervention.
- Recognizing potential misdiagnoses, such as age-related macular degeneration, is critical.
- This report underscores the need for comprehensive evaluation in suspected cases of choroidal osteoma.
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