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.

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