Spontaneous pneumothorax in a neonate with TEF and double oesophageal atresia. A case report

N. Tihitena, F. Temesgen
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Abstract

Symptomatic Spontaneous pneumothorax is uncommon disease scenario in term neonates. But pneumothorax can occur in neonates who had CPR or are on mechanical ventilator for different causes of respiratory distress. Congenital double esophageal atresia is a very rare type of esophageal atresia. If only single membranous atresia it can be isolated esophageal membranous atresia or with trachea-esophageal fistula. This type of atresia was not mentioned in gross or Vogt classification. Previously, only a few cases with an obstructing web had been reported and also multiple esophageal atresias. But there is no any documented case report with TEF & multiple esophageal atresia. The choices of treatment vary from ligation of the fistula with excision of the membrane by esophagotomy and/or gastrotomy, thoraco-abdominal approach and end to end anastomoses of the proximal & distal atresia. Here we present a case of a neonate who had developed respiratory distress since birth with a cause of tension spontaneous pneumothorax and managed by a chest tube and also diagnosed to have oesophageal atresia with distal tracheo-esophageal fistula on further evaluation and showing additional distal membranous oesophageal atresia during the thoracotomy. And he was managed accordingly. Keywords: Spontaneous Pneumothorax, esophageal atresia, Membranous atresia, TEF
新生儿自发性气胸伴TEF合并双食道闭锁1例。病例报告
摘要症状性自发性气胸在足月新生儿中并不常见。但气胸可能发生在接受心肺复苏术或因不同原因呼吸窘迫而使用机械呼吸机的新生儿身上。先天性双食道闭锁是一种非常罕见的食道闭锁类型。单侧膜性闭锁可合并食管膜性闭锁或合并气管-食管瘘。这种类型的闭锁在gross或Vogt分类中未被提及。在此之前,只有少数的梗阻腹壁和多发性食管闭锁的病例被报道过。但TEF合并多发性食管闭锁尚未见文献报道。治疗方法的选择不同,有通过食管和/或胃切开术结扎瘘并切除膜,胸腹入路和近端和远端闭锁端到端吻合。本文报告一例新生儿自出生以来出现呼吸窘迫,由紧张性自发性气胸引起,经胸管治疗,经进一步评估诊断为食管闭锁伴远端气管-食管瘘,并在开胸术中显示出额外的远端膜性食管闭锁。于是他就受到了相应的管理。关键词:自发性气胸,食管闭锁,膜性闭锁,TEF
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