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The prevalence of tracheal bronchus in pediatric patients undergoing rigid bronchoscopy

机译:接受硬支气管镜检查的小儿气管支气管患病率

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摘要

BACKGROUND: Tracheal bronchus (TB) is defined as an abnormal bronchus that originates directly from the lateral wall of the trachea above the carina and goes towards the upper lobe territory of the lung. We analyzed rigid endoscopies of the trachea in children to determine the incidence and characteristics of TB.\udMETHODS: In total, 1021 rigid endoscopies of the trachea recorded from children aged 0 to 6 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 origin of the TB and its level above the carina was noted. Data of the identified patients was reviewed for the presence of preoperative airway findings such as stridor, upper lobe pneumonia and wheezing or atelectasis, other congenital anomalies, and intraoperative complications.\udRESULTS: TB was detected in 11 (1.06%) of 1021 upper airway endoscopic examinations. All originated from the right lateral wall of the trachea. Six children had retained secretions in the TB, and 3 children had perioperative airway problems unrelated to the TB. One child showed right main stem bronchus narrowing as seen at the true carina, in the presence of a TB. All the children with TB exhibited at least 1 additional congenital anomaly at birth besides TB.\udCONCLUSIONS: TB is a relatively common congenital endoscopic lower airway anomaly in childhood, which is itself rarely symptomatic, but almost always coexists with other congenital anomalies.
机译:背景:气管支气管(TB)定义为异常支气管,其直接起源于隆起上方气管的侧壁并向肺的上叶区域延伸。我们分析了儿童气管的硬性内镜检查,以确定结核病的发生率和特征。\ udMETHODS:总共分析了0-21岁儿童记录的1021例气管的硬性内镜检查。使用0度霍普金斯棒状透镜望远镜从声门上区域到鼻腔进行内窥镜检查。确定了结核病患者,并指出了结核病的起源部位及其在隆突上方的水平。审查了所鉴定患者的数据,以检查是否存在术前气道发现,如喘鸣,上叶肺炎和喘息或肺不张,其他先天性异常以及术中并发症。\结果:在1021上气道中有11例(1.06%)检出了TB内窥镜检查。全部起源于气管的右侧壁。 6名儿童保留了结核中的分泌物,3名儿童有与结核无关的围手术期气道问题。在结核病的存在下,一个孩子的右主干支气管变窄,如在真正的隆突上所见。结论:TB是儿童期相对常见的先天性内镜下呼吸道异常,其本身很少有症状,但几乎与其他先天性异常共存。

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