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Anesthetic management of a neonate with laryngotracheoesophageal cleft and tracheoesophageal fistula

机译:喉气管食管裂隙和气管食管瘘的新生儿的麻醉处理

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摘要

Laryngotracheoesophageal cleft (LTEC) is an extremely rare congenital anomaly characterized by an absence of all or a part of the tracheoesophageal septum producing an abnormal communication between the trachea and esophagus, and is often difficult to be diagnosed. A 2-day-old male baby was tentatively diagnosed as tracheoesophageal fistula type Gross C, and underwent gastrostomy. The trachea was intubated before anesthetic induction. When a balloon of gastrostomy catheter was inflated, the lung could not be ventilated. After extubation of endotracheal tube and removal of gastrostomy catheter, the lung could be ventilated with mask. When endotracheal tube was intubated again, the lung could not be ventilated at all. Thus the surgery was performed under mask ventilation. Endoscopic examination performed 2 weeks later gave diagnosis of LTEC type 3. It is likely that the endotracheal tube might have been advanced into the end of the esophagus due to absence of the tracheoesophageal septum. In spite of a rare disease, LTEC should be considered as an extreme case of transesophageal fistula with a high risk of difficult airway.
机译:喉气管食管裂隙(LTEC)是一种极为罕见的先天性异常,其特征是不存在气管食管中隔的全部或部分,从而在气管和食道之间产生了异常的通讯,通常难以诊断。初步诊断为2天大的男婴为气管食管瘘型肉眼C型,并进行了胃造口术。麻醉诱导前先将气管插管。当胃造口术导管球囊膨胀时,肺无法通气。气管插管拔管并取出胃造口术导管后,可使用面罩使肺通气。再次向气管插管时,肺完全无法通气。因此,手术是在面罩通气下进行的。 2周后进行内镜检查,确诊为3型LTEC。由于气管食管隔膜的缺失,气管导管可能已经进入食管末端。尽管罕见病,LTEC仍应被认为是经食管瘘的极端病例,有高难度的气道危险。

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