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先天性肺畸形的结构和灌注磁共振成像。

Structural and perfusion magnetic resonance imaging of congenital lung malformations.

机构信息

Department of Diagnostic Imaging, University Children's Hospital Zürich, Steinwiesstr. 75, CH 8032, Zürich, Switzerland.

Children's Research Centre, University Children's Hospital Zürich, Zürich, Switzerland.

出版信息

Pediatr Radiol. 2020 Jul;50(8):1083-1094. doi: 10.1007/s00247-020-04658-5. Epub 2020 Apr 17.

Abstract

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.

摘要

背景

对于患有先天性胸畸形的幼儿,人们希望有一种无辐射的先进成像方式来进行检查。

目的

描述先天性支气管肺前肠畸形的磁共振成像(MRI)表现,并探讨肺 MRI 对其分类的能力。

材料和方法

这是对 39 名疑似先天性肺异常儿童连续进行 MRI 检查的回顾性分析(中位年龄:3.8 个月,范围:2 天-15 岁)。在 1.5 特斯拉时,通过呼吸门控快速自旋回波和动态对比增强序列获得形态和灌注发现。两名读者独立对异常情况进行分类,并与基于病理、手术和/或其他成像的专家诊断进行比较。

结果

主要诊断包括 33 例支气管肺病变、4 例肺下腔静脉综合征、1 例肺动静脉畸形和食管重复囊肿。在 46 个观察到的异常中,44 个(96%)被正确分类,观察者间一致性非常好(96%的一致性率)。39 个检测到的肺部病变包括孤立性过度膨胀(17/39,44%)、囊性肺气道畸形(8/39,21%)、支气管肺隔离症(7/39,18%)、支气管源性囊肿(4/39,10%)和混合病变(3/39,8%)。所有肺部病变在峰值肺强化时均表现为灌注缺陷。非囊性病变与正常肺实质相比,峰值延迟(中位数延迟:2.8s,四分位间距:0.5-4.0s)。

结论

包括呼吸补偿序列、动态血管造影和灌注的专用肺部 MRI 方案能够可靠地描绘先天性支气管肺前肠畸形的实质和血管成分。因此,MRI 可用于先天性胸畸形的综合产后评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88b5/7329781/bd015e5a1a45/247_2020_4658_Fig1_HTML.jpg

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