Hofmann U, Hofmann D, Vogl T, Wilimzig C, Mantel K
Department of Paediatric Anaesthesia, Dr. von Haunersches Kinderspital, University of Munich, FRG.
Prog Pediatr Surg. 1991;27:221-30. doi: 10.1007/978-3-642-87767-4_12.
Magnetic resonance imaging of the trachea was performed in 21 children with congenital or acquired narrowing of the trachea or main bronchi. Diagnosis included aortic arch anomalies, innominate artery compression, pulmonary artery compression and tracheomalacia. All patients were examined after bronchoscopy. The demonstration of the trachea and the surrounding tissue and vessels on MR images enables the cause of tracheal compression and the degree and location of collapse to be evaluated. MRI is a modality well suited to characterizing tracheal narrowing without employing ionizing radiation or intravenous contrast medium. All MRI examinations were carried out with the patient under general anaesthesia so as not to risk pulmonary deterioration during sedation. In the cases presented MRI is the diagnostic step of choice after tracheobronchoscopy and broadens the diagnostic potential in extrinsic tracheal or bronchial stenosis in paediatric patients.
对21例患有先天性或后天性气管或主支气管狭窄的儿童进行了气管磁共振成像检查。诊断包括主动脉弓异常、无名动脉压迫、肺动脉压迫和气管软化。所有患者均在支气管镜检查后接受检查。磁共振图像上气管及周围组织和血管的显示能够评估气管受压的原因以及塌陷的程度和位置。磁共振成像(MRI)是一种非常适合于在不使用电离辐射或静脉内造影剂的情况下对气管狭窄进行特征性描述的检查方式。所有磁共振成像检查均在患者全身麻醉下进行,以免在镇静过程中出现肺部恶化的风险。在本文所呈现的病例中,磁共振成像(MRI)是气管支气管镜检查后的首选诊断步骤,并且拓宽了小儿患者外在性气管或支气管狭窄的诊断潜力。