[两例先天性心脏异常合并食管闭锁]
[Two cases of congenital cardiac anomaly associated with esophageal atresia].
作者信息
Satoh Y, Iwaya F, Igari T, Satokawa H, Takase S, Hoshino S, Kanazawa Y, Konno M
机构信息
Department of Cardiovascular Surgery, Fukushima Medical College.
出版信息
Kyobu Geka. 1992 May;45(5):424-7.
Two cases of congenital cardiac anomaly associated with esophageal atresia and tracheo-esophageal fistula were presented. One case was HLHS, and the other was TAPVR. Esophageal procedures were performed earlier than cardiac procedures in both cases. Primary anastomosis for esophageal atresia just after birth in the latter case. Corrective procedures for cardiac anomalies were performed at 36 days and 35 days after birth, respectively. The HLHS case died perioperatively and the TAPVR case survived the operation and is alive one year postoperatively.
本文报告了两例先天性心脏畸形合并食管闭锁及气管食管瘘的病例。一例为左心发育不全综合征（HLHS），另一例为完全性肺静脉异位引流（TAPVR）。两例均先行食管手术，后行心脏手术。后一例出生后即行食管闭锁一期吻合术。心脏畸形矫正手术分别在出生后36天和35天进行。HLHS病例围手术期死亡，TAPVR病例手术存活，术后一年仍存活。
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