Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 Jun 27;2023(6):rjad371.
doi: 10.1093/jscr/rjad371. eCollection 2023 Jun.

Epibulbar osseous choristoma: a case report

Affiliations
Case Reports

Epibulbar osseous choristoma: a case report

Khitam Fakhir Alhasseny et al. J Surg Case Rep. .

Abstract

Peribulbar osseous choristoma is a benign, solid nodule; it is a subtype of epibulbar choristomas (belongs to single tissue choristomas), consisting of pure bony tissues. Epibulbar osseous choristoma is the rarest subtype of epibulbar choristomas, with only 65 cases reported since the mid-19th century; so, the rarity of the disease drove me to report it. A 7-year-old female presented with a painless left ocular superotemporal mass, which was present since birth and located under the conjunctiva. The primary diagnoses included lipodermoid and subconjunctival foreign bodies. Ocular interventions included a B-scan, examination under anesthesia and surgical excision of the mass in toto, and the histopathological examination showed that it was an osseous choristoma.

Keywords: choristoma; epibulbar.

PubMed Disclaimer

Conflict of interest statement

None declared.

Figures

Figure 1
Figure 1
Picture showing the subconjunctival mass with overlying dilated vessels.
Figure 2
Figure 2
(A) Picture showing the gross anatomy of this white osseus lesion during removal from the subconjunctival space; (B) histologically the lesion was composed of mature lamellated bone with Haversian system and may be surrounded by thin connective tissues capsule, rarely some may have bony trabeculae with marrow elements.

Similar articles

References

    1. Harkins KA, Perry D, Suh DW. Epibulbar osseous choristoma: a case report. Am J Ophthalmol Case Rep 2017;5:4–6. - PMC - PubMed
    1. Ponnudurai T, Louisraj S, Salman A. Epibulbar osseous choristoma: a case report. Int Med Case Rep J 2017;10:337–9. - PMC - PubMed
    1. Shanthala PR, Khandige S. Epibulbar osseous choristoma: a rare entity. J Evol Med Dent Sci 2013;2:5717–9.
    1. Balci O, Oduncu A. A case of epibulbar osseous choristoma with review of literature. Int Ophthalmol 2014;34:1145–8. - PubMed
    1. Parihar A, Verma S, Trehan A, Vashisht P. A case of epibulbar osseous choristoma. J Mar Med Soc 2018;20:157–8.

Publication types