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Published on: May 23, 2025
Surgical approach in a rare case of coloboma-choristoma
Andrea Spano1, Elena Piozzi, Maurizio Cavallini
1Department of Plastic and Reconstructive Surgery, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy. andreaspano@aliceposta.it
Insights
This study presents a rare case of combined upper eyelid coloboma and lower eyelid dermolipoma in an infant with a Tessier cleft. A novel surgical technique achieved a successful functional and cosmetic repair of the congenital eyelid defect.
Area of Science:
- Ophthalmology
- Plastic Surgery
- Pediatric Surgery
Background:
- Congenital eyelid defects, including coloboma and dermolipoma, can occur in isolation or with craniofacial anomalies.
- Tessier craniofacial clefts represent a spectrum of congenital malformations affecting the face and skull.
Purpose of the Study:
- To describe the rare co-occurrence of upper eyelid coloboma and lower eyelid dermolipoma in an infant with a Tessier no. 0-1 cleft.
- To present a surgical technique for correcting congenital palpebral coloboma using specific tissue grafts.
Main Methods:
- Surgical intervention involving a flap of subconjunctival choristoma.
- Grafting of reshaped cutaneous and tarsal portions from a preauricular anlage.
- Correction of congenital upper eyelid coloboma and lower eyelid dermolipoma.
Main Results:
- The described surgical technique resulted in a virtually complete repair of the congenital eyelid defect.
- An acceptable functional and cosmetic outcome was achieved post-operatively.
- Demonstrated successful management of a complex congenital eyelid malformation.
Conclusions:
- The presented surgical approach is effective for correcting congenital palpebral coloboma, particularly in complex cases.
- This technique offers a viable solution for managing combined eyelid defects associated with craniofacial anomalies.
- Highlights the importance of tailored surgical strategies for rare congenital eyelid malformations.
Abstract:
Embryogenic eyelid defects can be isolated or associated with malformative diseases, such as Tessier craniofacial clefts. We describe the exceptional coexistence of upper eyelid coloboma and lower eyelid dermolipoma in a 45-day-old infant with a Tessier no. 0-1 cleft. The surgical intervention carried out on this patient, which used a flap of subconjunctival choristoma and grafting of reshaped cutaneous and tarsal portions of a preauricular anlage, is presented as a technique for correcting congenital palpebral coloboma. Adoption of this technique allowed virtually complete repair of the defect and gave an acceptable functional and cosmetic result.
