Peri Operative Management of a Simultaneously Symptomatic Diaphragmatic Hernia and Imperforate Anus in a Neonate: A Rare but Challenging Combination

A. Ratnayake
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Abstract

Congenital diaphragmatic hernia a rare congenital malformation which often requires surgical interventions. The surgery is not an emergency, and it can be done within days with planned preoperative optimisation. We present a case of a premature neonate presented with co-existence of left side diaphragmatic hernia with imperforate anus. Presence of imperforate anus prevents the passage of meconium leading to distention of bowel increasing the resistance inside the left hemithorax. Therefore, an urgent repair of the diaphragmatic hernia with colostomy formation was done under general anaesthesia after 48 hours of birth. Patient was managed in a paediatric intensive care unit both pre and post operative period. Even though the post operative period was complicated with a broncopneumonia and a pleural effusion, he was discharged from ICU 20 days after the procedure.
新生儿同时出现症状的膈疝和肛门闭锁的围手术期处理:一种罕见但具有挑战性的组合
先天性膈疝是一种罕见的先天性畸形,通常需要手术干预。手术不是紧急情况,可以在几天内完成,并计划进行术前优化。我们报告一例早产新生儿并发左侧膈疝及肛门闭锁。肛门闭锁可阻止胎粪通过,导致肠道扩张,增加左半胸内的阻力。因此,在分娩48小时后,在全身麻醉下进行了带结肠造口的膈疝紧急修复。患者在术前和术后均在儿科重症监护室接受治疗。尽管术后并发支气管肺炎和胸腔积液,但他在手术后20天就从重症监护室出院了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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