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Lacrimal gland choristoma of the ciliary body
Hee Yoon Cho1, Ho-Seok Sa, Se Woong Kang
1Department of Ophthalmology, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.
Insights
This study reports a rare case of lacrimal gland choristoma in an infant's ciliary body, alongside orbital cellulitis. Early diagnosis and surgical removal led to a favorable outcome, highlighting the importance of considering this in pediatric ciliary body masses.
Area of Science:
- Ophthalmology
- Pediatric Oncology
- Pathology
Background:
- Lacrimal gland choristoma is an exceptionally rare condition when presenting within the ciliary body.
- This case involves an infant diagnosed with a ciliary body mass and concurrent orbital cellulitis.
Observation:
- A 10-month-old female infant presented with right upper eyelid swelling and tenderness, indicative of orbital cellulitis.
- Ophthalmic examination revealed a fleshy mass in the superotemporal ciliary body, detected incidentally during funduscopy.
- Pathologic examination confirmed the mass as a lacrimal gland choristoma with an epithelial-lined cyst.
Findings:
- Surgical resection of the ciliary body mass was performed.
- The patient experienced no hypotonia or lesion enlargement one year post-surgery, indicating successful treatment.
- Histopathology confirmed lacrimal gland choristoma with an associated epithelial-lined cyst.
Implications:
- Lacrimal gland choristoma should be considered in the differential diagnosis for pediatric patients presenting with ciliary body masses.
- This case underscores the importance of thorough ophthalmic examination in infants with suspected orbital inflammation.
- Prompt diagnosis and surgical intervention can lead to positive outcomes for rare pediatric ocular tumors.
Background:
Lacrimal gland choristoma manifesting in the ciliary body is quite rare. We report a case of lacrimal gland choristoma manifesting in the ciliary body, coupled with orbital cellulites, in an infant.
Case:
A 10-month-old female infant with swelling and tenderness of the right upper eyelid.
Observations:
The results of ophthalmic examinations of the patient were consistent with orbital cellulitis. During the funduscopic examination, a fleshy mass was incidentally detected at the superotemporal portion of the ciliary body in the right eye. A local resection of the lesion was carried out. The results of a pathologic examination showed lacrimal gland choristoma of the ciliary body that was accompanied by an epithelia-lined cyst. The patient has had no hypotonia or enlargement of the lesion for 1 year after surgery.
Conclusion:
Lacrimal gland choristoma should be included in the differential diagnosis of a ciliary body mass in pediatric patients.
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