Abdul Rahim Faizah, Goh Bee See
Department of Otorhinolaryngology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre (UKMMC), Jalan Yaacob Latif, Bandar Tun Razak, 56000 Cheras, Kuala Lumpur Malaysia.
Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):2666-2669. doi: 10.1007/s12070-020-02358-y. Epub 2021 Jan 19.
Tracheal bronchus (TB) is a rare congenital anomaly described as a abnormal bronchus that originates directly from the trachea above the carina directed towards the upper lung lobe. We analysed all paediatric rigid endoscopies of the airway from January 2015 until August 2020 to determine the incidence and characteristic of TB. In total, 68 rigid endoscopic airway examination record from children aged 0 to 12 years were analyzed. Endoscopic examination was performed from supraglottic region to carina using a 0 degree Hopkins rod lens telescope. Patients with a TB were identified and the site of TB origin was noted. Data of the identified patients was reviewed for the presence of preoperative airway findings such as stridor, upper lobe pneumonia, other congenital anomalies, intraoperative findings and complications and postoperative general condition outcome. TB was detected in 8 (11.8%) of 68 airway endoscopic examinations. 6 children (75%) were syndromic. 5 patients (62.5%) has congenital malacic airway and 2 patients (25%) has congenital tracheal stenosis. All TB originated from the right lateral wall of the trachea. All children had stridor unrelated to TB as presentation and 4 (50%) of children had preoperative upper lobe pneumonia. Tracheal bronchus is not a rare finding and is highly associated with syndromes and other airway anomalies. Although children with TB can be asymptomatic, upper lobe pneumonia is a common presentation. TB should be included in the differential diagnosis in patients with recurrent right upper lobe pneumonia or collapse and patients with unexplained oxygenation problem during endotracheal intubation, particularly in children with syndromes or other congenital anomalies.
气管支气管(TB)是一种罕见的先天性异常,被描述为直接起源于气管隆突上方并朝向肺上叶的异常支气管。我们分析了2015年1月至2020年8月期间所有儿科气道硬式内镜检查,以确定气管支气管的发病率和特征。总共分析了68例0至12岁儿童的气道硬式内镜检查记录。使用0度Hopkins杆状透镜望远镜从声门上区域到隆突进行内镜检查。识别出患有气管支气管的患者,并记录气管支气管的起源部位。回顾已识别患者的数据,以了解术前气道检查结果,如喘鸣、上叶肺炎、其他先天性异常、术中发现和并发症以及术后一般状况。在68例气道内镜检查中,有8例(11.8%)检测到气管支气管。6名儿童(75%)患有综合征。5例患者(62.5%)有先天性软化气道,2例患者(25%)有先天性气管狭窄。所有气管支气管均起源于气管右侧壁。所有儿童均以与气管支气管无关的喘鸣为表现,4名儿童(50%)术前有上叶肺炎。气管支气管并非罕见发现,且与综合征及其他气道异常高度相关。尽管患有气管支气管的儿童可能无症状,但上叶肺炎是常见表现。对于反复出现右上叶肺炎或肺不张的患者以及在气管插管期间出现不明原因氧合问题的患者,尤其是患有综合征或其他先天性异常的儿童,应将气管支气管纳入鉴别诊断。