先天性食管闭锁长间隙型的外科处理
摘要
先天性食管闭锁是新生儿期消化道一种严重的发育畸形，发病率约1／3000活产儿。此病在发病机理和诊治中目前存在很多热点问题，如：合伴多发性畸形，术后胃食管返流、气管软化、远端食管动力学、食管气管瘘复发及长间隙型的外科处理等。
出处
《临床外科杂志》
2010年第8期505-506,共2页
Journal of Clinical Surgery
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