Bilateral Episcleral Osseous Choristoma

PURPOSE: To report the symmetric masses developed in both eyes, which were diagnosed with bilateral osseous choristoma and surgically excised. METHODS: A 6-year-old female was noted by her parents to have a mass under the conjunctiva of her left eye. The mass was white and firmly attached to the globe. The same lesion was present in the right eye. CT scan showed that the masses were high bone-density and did not invade the sclera deeply. Therefore, excisional biopsy of the lesions were performed. RESULTS: Histopathologic examination showed that the masses were episcleral osseous choristoma. There was no complication of recurrence or adhesion after surgery. CONCLUSIONS: In case of a hard mass under the conjunctiva, which is diagnosed with osseous choristoma by CT scanning, it is helpful to determine the accurate location and adhesion of the massfor successful surgery.

A Case of Lingual Osseous Choristoma / 대한이비인후과학회지

The term "choristoma" is used to describe a mass of histologically normal tissue presenting in an aberrant site. The authors have experienced a case of lingual osseous choristoma in a 17-year-old female patient, which was totally removed and followed up for 12 months without any evidence of recurrence or developments to other disease.

Osseous Choristoma within an Epibulbar Complex Choristoma

Episcleral osseous choristoma is a rare isolated bony nodule occurring in the conjunctival or episcleral connective tissue in eyes which are otherwise normal. They are present at birth. This congenital lesion is usually about the size of a pea and typically located in the superotemporal quadrant, some 5 to 10mm from the limbus. Of the 40 reported cases in the literature, none had associated ocular abnormalities. The diagnosis has seldom been suspected preoperatively. Our patient was 3-month-old healthy male baby. For the cosmetic purpose, we had done excisional biopsy. In the histopathologic study, the mass was a dermoid covered with skin and contained fat, hair follicle and osseous tissue at its center. The mass was confirmed to be a complex choristoma, especially osseous choristoma. We report this case because of the rarity of osseous chroistomas combined with complex choristoma.