Pediatric Radiology and Neuroradiology, ASST Fatebenefratelli-Sacco Milano, Children's Hospital V. Buzzi, Via Castelvetro 32, 20154, Milan, Italy.
Radiology, Ospedale della Murgia F. Perinei, Altamura, BA, Italy.
Eur Radiol. 2019 Sep;29(9):4544-4554. doi: 10.1007/s00330-019-06042-w. Epub 2019 Feb 22.
To compare postnatal magnetic resonance imaging (MRI) with the reference standard computed tomography (CT) in the identification of the key features for diagnosing different types of congenital lung malformation (CLM).
Respiratory-triggered T2-weighted single-shot turbo spin echo (ss-TSE), respiratory-triggered T1-weighted turbo field echo (TFE), balanced fast field echo (BFFE), and T2-weighted MultiVane sequences were performed at 1.5 T on 20 patients prospectively enrolled. Two independent radiologists examined the postnatal CT and MRI evaluating the presence of cysts, hyperinflation, solid component, abnormal arteries and/or venous drainage, and bronchocele. Diagnostic performance of MRI was calculated and the agreement between the findings was assessed using the McNemar-Bowker test. Interobserver agreement was measured with the kappa coefficient.
CT reported five congenital pulmonary airway malformations (CPAMs), eight segmental bronchial atresias, five bronchopulmonary sequestrations (BPS), one congenital lobar overinflation, one bronchogenic cyst, and three hybrid lesions. MRI reported the correct diagnosis in 19/20 (95%) patients and the malformation was correctly classified in 22/23 cases (96%). MRI correctly identified all the key findings described on the CT except for the abnormal vascularization (85.7% sensitivity, 100% specificity, 100% PPV, 94.1% NPV, 95% accuracy for arterial vessels; 57.1% sensitivity, 100% specificity, 100% PPV, 84.2% NPV, 87% accuracy for venous drainage).
MRI can represent an effective alternative to CT in the postnatal assessment of CLM. In order to further narrow the gap with CT, the use of contrast material and improvements in sequence design are needed to obtain detailed information on vascularization, which is essential for surgical planning.
• Congenital lung malformations (CLMs) can be effectively studied by MRI avoiding radiation exposure. • Crucial features of CLM have similar appearance when comparing CT with MRI. • MRI performs very well in CLM except for aberrant vessel detection and characterization.
比较产后磁共振成像(MRI)与参考标准计算机断层扫描(CT)在识别不同类型先天性肺畸形(CLM)的诊断特征方面的差异。
前瞻性纳入 20 例患者,在 1.5T 上进行呼吸触发 T2 加权单次激发涡轮自旋回波(ss-TSE)、呼吸触发 T1 加权涡轮场回波(TFE)、平衡快速场回波(BFFE)和 T2 加权多叶序列扫描。两位独立的放射科医生评估了 CT 和 MRI 的结果,以评估是否存在囊肿、过度充气、实性成分、异常动脉和/或静脉引流以及支气管扩张。计算 MRI 的诊断性能,并使用 McNemar-Bowker 检验评估发现之间的一致性。采用kappa 系数评估观察者间的一致性。
CT 报告了 5 例先天性肺气道畸形(CPAMs)、8 例节段性支气管闭锁、5 例肺隔离症(BPS)、1 例先天性肺过度充气、1 例支气管囊肿和 3 例混合病变。MRI 在 20/20(95%)例患者中正确诊断,22/23(96%)例患者中正确分类畸形。MRI 正确识别了 CT 上描述的所有关键发现,除了异常血管化(85.7%的敏感性、100%的特异性、100%的阳性预测值、94.1%的阴性预测值、95%的动脉血管准确性;57.1%的敏感性、100%的特异性、100%的阳性预测值、84.2%的阴性预测值、87%的静脉引流准确性)。
MRI 可作为 CLM 产后评估的有效替代方法,避免辐射暴露。为了进一步缩小与 CT 的差距,需要使用对比材料和改进序列设计,以获得对血管化的详细信息,这对手术计划至关重要。
先天性肺畸形(CLM)可通过 MRI 进行有效研究,避免辐射暴露。
CT 与 MRI 比较时,CLM 的关键特征具有相似的表现。
MRI 在 CLM 中的表现非常出色,除了异常血管检测和特征描述外。