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Epibulbar Complex Choristoma Containing Bone: A Case Report and Closer Look at Classifications.

Authors :
Angus ZG
McKelvie P
Hardy TG
Source :
Case reports in ophthalmology [Case Rep Ophthalmol] 2024 May 08; Vol. 15 (1), pp. 418-422. Date of Electronic Publication: 2024 May 08 (Print Publication: 2024).
Publication Year :
2024

Abstract

Introduction: Epibulbar choristoma is a benign congenital lesion containing histologically normal-appearing tissue in an abnormal ectopic location. An epibulbar choristoma is classified as either epibulbar dermoid, dermolipoma, or complex choristoma based on histological examination. The case presented was a presumed epibulbar dermolipoma with no signs of ossification on imaging, examination, or intraoperatively until the specimen was examined histologically, clarifying the lesion as an epibulbar complex choristoma. Reassuringly, the presence of bone in such lesions should not change management.<br />Case Presentation: A mother noticed a small fleshy mass on her 9-year-old daughter's superotemporal bulbar conjunctiva. The suspected epibulbar dermolipoma was confirmed with MRI and initially managed conservatively. Two years later, she was referred for apparent growth and cosmetic concerns, and she underwent surgical debulking.<br />Conclusion: We present this case for its unusual presentation and histological findings. Orbital surgeons should be aware of the possibility of ossification of epibulbar choristomas and avoid confusion with alternative diagnoses. Clarification of the latest classification system for epibulbar choristomas is provided.<br />Competing Interests: The authors have no conflicts of interest to declare.<br /> (© 2024 The Author(s). Published by S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1663-2699
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Case reports in ophthalmology
Publication Type :
Report
Accession number :
38721041
Full Text :
https://doi.org/10.1159/000538824