一名早产新生儿患先天性膈疝，并伴有食管闭锁、气管食管瘘和动脉干。
Congenital diaphragmatic hernia associated with esophageal atresia, tracheoesophageal fistula, and truncus arteriosus in a premature newborn.
作者信息
Cunát V, Stranák Z, Pýcha K, Tláskal T, Melichar J, Miletín J, Janota J, Kucera J, Velebil P
机构信息
Neonatal Intensive Care Unit, Institute for the Care of Mother and Child, Podolské nábrezí 157, Praha 4, Prague 14710, Czech Republic.
出版信息
Pediatr Surg Int. 2005 Aug;21(8):684-6. doi: 10.1007/s00383-005-1443-4. Epub 2005 Oct 13.
The occurrence of coexisting congenital diaphragmatic hernia (CDH) and esophageal atresia (EA) with distal tracheoesophageal fistula (TEF) is extremely rare and is considered highly lethal. The combination of CDH with EA/TEF and truncus arteriosus communis (TAC) has not been reported in the literature to date. The authors describe a premature neonate with this association.
先天性膈疝（CDH）与食管闭锁（EA）合并远端气管食管瘘（TEF）同时存在的情况极为罕见，且被认为具有高度致死性。迄今为止，文献中尚未报道过CDH合并EA/TEF与共同动脉干（TAC）的病例。作者描述了一名患有这种联合病症的早产儿。
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