Department of Anaesthesiology, Weifang People's Hospital, Weifang, China.
J Int Med Res. 2020 Oct;48(10):300060520967609. doi: 10.1177/0300060520967609.
A tracheal bronchus is a rare congenital anomaly, suggesting abnormal bronchial development. The prevalence of tracheal bronchus in children who undergo bronchoscopy is estimated to be between 0.2% and 3%. When associated with recurrent infection, lobes of the lung must be removed to avoid further lung injury. In such cases, perioperative one-lung ventilation and airway management remain a huge challenge for anaesthesiologists. The case of this rare airway anatomic abnormality in a paediatric patient with two bronchial openings into the right upper lobe, and with a history of recurrent pneumonia, is reported. In addition to a normal opening, a distinct opening in the upper lobe of the right lung was observed, that originated directly from the trachea, superior to the carina. The entire right lung was deflated by left-lung ventilation using a single lumen tracheal tube, and the patient underwent right upper lobe resection. No anaesthesia complications were observed during recovery. In this case, timely identification of the tracheal bronchus and successful collapse of the right lung were key points in the anaesthesia management of this patient.
气管支气管是一种罕见的先天性异常,提示支气管发育异常。在接受支气管镜检查的儿童中,气管支气管的患病率估计在 0.2%至 3%之间。当与反复感染相关时,必须切除肺叶以避免进一步的肺损伤。在这种情况下,围手术期单肺通气和气道管理仍然是麻醉师面临的巨大挑战。本文报告了一例罕见的气道解剖异常病例,患儿右上肺有两个支气管开口,且有反复肺炎病史。除了正常开口外,还观察到右肺上叶有一个明显的开口,该开口直接从气管起源,位于隆突上方。通过左侧单腔气管导管通气使整个右肺萎陷,并进行右上肺叶切除术。在恢复过程中未观察到麻醉并发症。在这种情况下,及时识别气管支气管并成功使右肺萎陷是该患者麻醉管理的关键。