Open Medicine
(Jan 2016)
Sternal reconstruction by extracellular matrix: a rare case of phaces syndrome
Molinaro Francesco,
Garzi Alfredo,
Cerchia Elisa,
Di Crescenzo Vincenzo Giuseppe,
Luzzi Luca,
Bulotta Anna Lavinia,
Gotti Giuseppe,
Messina Mario
Affiliations
Molinaro Francesco
Division of Pediatric Surgery, Department of Medical, Surgical and Neurological Sciences, University of Siena, Italy
Garzi Alfredo
University Salerno, Salerno, Italy
Cerchia Elisa
Department of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, Italy
Di Crescenzo Vincenzo Giuseppe
Department of Medicine and Surgery, Thoracic Surgery Unit, University of Salerno, Italy
Luzzi Luca
Thoracic Surgery Unit, University Hospital of Siena, Siena, Italy
Bulotta Anna Lavinia
Department of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, Italy
Gotti Giuseppe
Thoracic Surgery Unit, University Hospital of Siena, Siena, Italy
Messina Mario
Department of Medical, Surgical and Neurological Science. Pediatric Surgery Unit, University of Siena, Italy
DOI
https://doi.org/10.1515/med-2016-0037
Journal volume & issue
Vol. 11,
no. 1
pp.
196
– 199
Abstract
Read online
Congenital defects of the sternum are rare and due to a failure of midline development and fusion of the sternal bones. Surgical correction of a sternal cleft should be preferred during infancy for functional reasons. Chest wall reconstruction represented a complex problem in the last decades.
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