Repair of congenital sternal clefts in adolescence and infancy

Two cases of sternal cleft not associated with ectopia cordis are presented. An 11-year-old girl with a superior incomplete sternal cleft underwent reconstruction of the sternum with autologous rib, cartilage, and sternal periosteum. At the 1-year follow-up her sternal appearance was normal. The sec...

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Bibliographic Details
Published in:Journal of pediatric surgery Vol. 29; no. 12; p. 1513
Main Authors: Knox, L, Tuggle, D, Knott-Craig, C J
Format: Journal Article
Language:English
Published: United States 01-12-1994
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Summary:Two cases of sternal cleft not associated with ectopia cordis are presented. An 11-year-old girl with a superior incomplete sternal cleft underwent reconstruction of the sternum with autologous rib, cartilage, and sternal periosteum. At the 1-year follow-up her sternal appearance was normal. The second patient, a full-term baby girl, had complete sternal cleft diagnosed by ultrasonography at 21 weeks' gestation. She underwent primary repair in the neonatal period and currently is asymptomatic with a normal-appearing sternum (10 months postoperatively). Primary repair in the neonatal period is the best type of management for this rare condition. For older patients, autologous repair is appropriate and avoids problems associated with the use of prosthetic materials.
ISSN:0022-3468
DOI:10.1016/0022-3468(94)90198-8