Structural and perfusion magnetic resonance imaging of congenital lung malformations

被引:14
|
作者
Kellenberger, Christian J. [1 ,2 ]
Amaxopoulou, Christina [1 ,2 ]
Moehrlen, Ueli [2 ,3 ]
Bode, Peter K. [4 ]
Jung, Andreas [2 ,5 ]
Geiger, Julia [1 ,2 ]
机构
[1] Univ Childrens Hosp Zurich, Dept Diagnost Imaging, Steinwiesstr 75, CH-8032 Zurich, Switzerland
[2] Univ Childrens Hosp Zurich, Childrens Res Ctr, Zurich, Switzerland
[3] Univ Childrens Hosp Zurich, Dept Pediat Surg, Zurich, Switzerland
[4] Univ Zurich, Univ Hosp Zurich, Inst Pathol, Zurich, Switzerland
[5] Univ Childrens Hosp Zurich, Div Pulmonol, Zurich, Switzerland
关键词
Bronchopulmonary malformation; Children; Lung; Magnetic resonance imaging; Perfusion imaging; NATURAL-HISTORY; CHILDREN; LESIONS; DIAGNOSIS; PATHOLOGY; MANAGEMENT; RADIATION; DISEASE;
D O I
10.1007/s00247-020-04658-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background A radiation-free advanced imaging modality is desirable for investigating congenital thoracic malformations in young children. Objective To describe magnetic resonance imaging (MRI) findings of congenital bronchopulmonary foregut malformations and investigate the ability of lung MRI for their classification. Materials and methods This is a retrospective analysis of consecutive MRI examinations performed for suspected congenital lung anomalies in 39 children (median age: 3.8 months, range: 2 days-15 years). Morphological and perfusion findings were characterised on respiratory-gated fast spin echo and dynamic contrast-enhanced sequences obtained at 1.5 tesla. Abnormalities were classified independently by two readers and compared to an expert diagnosis based on pathology, surgery and/or other imaging. Results Main diagnoses included bronchopulmonary lesions in 33 patients, scimitar syndrome in 4 patients, pulmonary arteriovenous malformation and oesophageal duplication cyst in one patient each. Of 46 observed abnormalities, 44 (96%) were classified correctly with very good interobserver agreement (96% concordance rate). The 39 detected lung lesions included isolated overinflation (17/39, 44%), cystic pulmonary airway malformation (8/39, 21%), bronchopulmonary sequestration (7/39, 18%), bronchogenic cyst (4/39, 10%) and hybrid lesion (3/39, 8%). All lung lesions presented as perfusion defect at peak pulmonary enhancement. Non-cystic lesions showed a delayed peak (median delay: 2.8 s, interquartile range: 0.5 to 4.0 s) in relation to normal lung parenchyma. Conclusion A dedicated lung MRI protocol including respiratory compensated sequences, dynamic angiography and perfusion is able to reliably delineate parenchymal and vascular components of congenital bronchopulmonary foregut malformations. Therefore, MRI may be considered for comprehensive postnatal evaluation of congenital thoracic malformations.
引用
收藏
页码:1083 / 1094
页数:12
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