Molinaro Francesco, Garzi Alfredo, Cerchia Elisa, Di Crescenzo Vincenzo Giuseppe, Luzzi Luca, Bulotta Anna Lavinia, Gotti Giuseppe, Messina Mario
Division of Pediatric Surgery, Department of Medical, Surgical and Neurological Sciences, University of Siena, Italy.
University Salerno, Salerno, Italy.
Open Med (Wars). 2016 Jun 23;11(1):196-199. doi: 10.1515/med-2016-0037. eCollection 2016.
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. We report our successful outcome of sternal reconstruction in a rare case of PHACES syndrome, in which the patient was submitted to reconstruction of the sternum and complete closure of the thoracic defect by the employ of an extracellular matrix XCM Biologic tissue matrix. We promote the use of extracellular matrix in surgical reconstruction of chest defects for its maneuverability, plasticity, tolerability and the possibility of growing with the children's chest getting a good compliance and optimal cosmetic results.
先天性胸骨缺损较为罕见,是由于胸骨中线发育及胸骨骨融合失败所致。出于功能原因,胸骨裂的手术矫正应在婴儿期进行。在过去几十年中,胸壁重建是一个复杂的问题。我们报告了在一例罕见的PHACES综合征患者中进行胸骨重建的成功结果,该患者通过使用细胞外基质(XCM生物组织基质)进行了胸骨重建及胸壁缺损的完全闭合。我们提倡在胸部缺损的手术重建中使用细胞外基质,因为它具有可操作性、可塑性、耐受性,并且有可能随着儿童胸部生长,从而获得良好的顺应性和最佳的美容效果。