Subscribe to RSS
DOI: 10.1055/s-0038-1673620
Fetal Congenital Peripheral Bronchial Atresia Diagnosed by Magnetic Resonance Imaging: Two Case Reports
Publication History
25 April 2018
21 August 2018
Publication Date:
09 October 2018 (online)
Abstract
Two types of congenital bronchial atresia (proximal and peripheral) have been classified. We report two cases of peripheral bronchial atresia diagnosed by prenatal ultrasonography (US) and magnetic resonance imaging (MRI). Evaluating an enlarged lung mass that is homogeneously hyperechoic on US and hyperintense on T2-weighted MRI can help in determining whether bronchial atresia is present. Proximal type is suggested when a dilated main bronchus is observed as a tubule structure of an involved lung hilum. In our cases, T2-weighted MRI revealed homogeneously hyperintense lung lesion with decreased signal intensity of adjacent lobe, flattening diaphragm, and mediastinal shift. Dilatation of the main bronchus was not observed and the opposite lung was normal in appearance. These findings were explained by secondary compression due to enlargement of the involved lung. The preservation of vascular structure and the retained normal shape, though enlarged, in the affected lobe were observed, which demonstrated undisrupted pulmonary architecture of the lobe. Thus, congenital cystic adenomatoid malformation was excluded because pulmonary architecture was relatively preserved. Finally, presumed diagnoses of the peripheral bronchial atresia were made and confirmed by postnatal chest computed tomography.
-
References
- 1 Berrocal T, Madrid C, Novo S, Gutiérrez J, Arjonilla A, Gómez-León N. Congenital anomalies of the tracheobronchial tree, lung, and mediastinum: embryology, radiology, and pathology. Radiographics 2004; 24 (01) e17
- 2 Langston C. New concepts in the pathology of congenital lung malformations. Semin Pediatr Surg 2003; 12 (01) 17-37
- 3 Kunisaki SM, Fauza DO, Nemes LP. , et al. Bronchial atresia: the hidden pathology within a spectrum of prenatally diagnosed lung masses. J Pediatr Surg 2006; 41 (01) 61-65 , discussion 61–65
- 4 Alamo L, Gudinchet F, Reinberg O. , et al. Prenatal diagnosis of congenital lung malformations. Pediatr Radiol 2012; 42 (03) 273-283
- 5 Cannie M, Jani J, De Keyzer F. , et al. Magnetic resonance imaging of the fetal lung: a pictorial essay. Eur Radiol 2008; 18 (07) 1364-1374
- 6 Alamo L, Reinberg O, Vial Y, Gudinchet F, Meuli R. Comparison of foetal US and MRI in the characterisation of congenital lung anomalies. Eur J Radiol 2013; 82 (12) e860-e866
- 7 Zamora IJ, Sheikh F, Olutoye OO. , et al. Mainstem bronchial atresia: a lethal anomaly amenable to fetal surgical treatment. J Pediatr Surg 2014; 49 (05) 706-711
- 8 Abitayeh G, Ruano R, Martinovic J, Barthe B, Aubry MC, Benachi A. Prenatal diagnosis of main stem bronchial atresia using 3-dimensional ultrasonographic technologies. J Ultrasound Med 2010; 29 (04) 633-638
- 9 Alamo L, Vial Y, Gengler C, Meuli R. Imaging findings of bronchial atresia in fetuses, neonates and infants. Pediatr Radiol 2016; 46 (03) 383-390
- 10 Peranteau WH, Merchant AM, Hedrick HL. , et al. Prenatal course and postnatal management of peripheral bronchial atresia: association with congenital cystic adenomatoid malformation of the lung. Fetal Diagn Ther 2008; 24 (03) 190-196
- 11 Epelman M, Kreiger PA, Servaes S, Victoria T, Hellinger JC. Current imaging of prenatally diagnosed congenital lung lesions. Semin Ultrasound CT MR 2010; 31 (02) 141-157