Luis A L, López Gutierrez J C, Fernández A, Avila L F, Encinas J L, Andrés A M, Hernández F, Nistal M, Tovar J A
Department of Paediatric Surgery, Hospital Universitario La Paz, Madrid, Spain.
Eur J Pediatr Surg. 2007 Aug;17(4):275-7. doi: 10.1055/s-2007-965418.
We present the case of a newborn with sternal cleft (SC) and presternal enterogenous cyst operated on during the neonatal period. SC is an uncommon congenital malformation of the thoracic wall which can occur as an isolated form or in association with other malformations. To our knowledge, the presence of SC and enterogenous cyst has not been described to date. Early surgical repair of SC gives good aesthetic and functional results and is usually the preferred approach.
我们报告了一例新生儿期接受胸骨裂(SC)和胸骨前肠源性囊肿手术的新生儿病例。胸骨裂是一种不常见的胸壁先天性畸形,可单独出现或与其他畸形并存。据我们所知,迄今为止尚未有胸骨裂与肠源性囊肿同时存在的报道。胸骨裂的早期手术修复可取得良好的美学和功能效果,通常是首选的治疗方法。