Superior sternal cleft: construction with a titanium plate
A Hazari1, N S Mercer, A Pawade
1Frenchay Hospital, Bristol, United Kingdom.
Insights
This study details a rare superior sternal cleft case in a neonate, associated with cervicofacial hemangiomata and cardiac defects. Early surgical repair using titanium plates is recommended for optimal outcomes in sternal cleft deformities.
Area of Science:
- Pediatric Surgery
- Congenital Malformations
- Cardiovascular Surgery
Background:
- Sternal cleft is a rare congenital deformity, with superior sternal cleft being the most common type.
- Sternal clefting is often associated with vascular dysplasia, but specific co-occurrences can be rare.
Observation:
- This report presents the first documented case of a superior sternal cleft in a neonate with cervicofacial hemangiomata and cardiac defects.
- The neonate did not exhibit true ectopia cordis, distinguishing this case from others with severe sternal defects.
Findings:
- Early surgical intervention for sternal clefting, ideally within the first four weeks of life, is advocated.
- The recommended surgical approach involves primary approximation, reinforced with a titanium plate for rigid internal fixation and reduced tension.
- Titanium plates promote osseointegration, leading to a stable, solid bony sternum post-repair.
Implications:
- This case highlights a unique association of congenital anomalies, emphasizing the need for comprehensive evaluation in neonates with sternal clefts.
- The proposed surgical technique using titanium plates offers a robust solution for sternal approximation, improving long-term stability.
- Timely surgical management is crucial for improving outcomes in neonates with sternal cleft deformities and associated conditions.
Abstract:
Sternal cleft is a rare congenital deformity, with a superior cleft being the most common. Although sternal clefting is known to be associated with vascular dysplasia, to our knowledge, we report the first case of superior sternal cleft with cervicofacial hemangiomata and cardiac defects in the absence of true ectopia cordis in a neonate. Early surgery in all cases of sternal clefting is advocated, preferably within the first 4 weeks of life. However, if the child is unfit for operation at this stage, repair should be carried out as soon as the child is stable and fit. The method of choice is primary approximation with the intraoperative precaution of confirming cardiorespiratory stability. We suggest reinforcing the primary approximation with a titanium plate to achieve rigid internal fixation and to reduce the tension at the approximation site. Because titanium osseointegrates well, this procedure results in a solid bony sternum.
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