Diagnostic accuracy of imaging studies in congenital lung malformations

Arch Dis Child Fetal Neonatal Ed. 2019 Jul;104(4):F372-F377. doi: 10.1136/archdischild-2018-314979. Epub 2018 Jul 26.

Abstract

Background: Although fetal ultrasound, fetal MRI and postnatal CT are now widely used in the evaluation of congenital lung malformations (CLM), their diagnostic accuracy remains undefined.

Objective: To correlate prenatal and postnatal imaging studies with pathological data after CLM resection.

Design: Retrospective, descriptive case series study.

Setting: A North American tertiary care centre.

Patients: One hundred and three consecutive lung resections for a suspected CLM between 1 January 2005 and 31 December 2015.

Main outcome measures: Diagnostic accuracy of imaging diagnosis compared with pathological evaluation.

Results: Pathological diagnoses included congenital pulmonary airway malformation ((CPAM) n=45, 44%), bronchopulmonary sequestration (BPS; n=25, 24%), CPAM/BPS hybrid lesions (n=22, 21%) and pleuropulmonary blastoma (n=2, 2%). Fetal ultrasound detected 85 (82.5%) lesions and correctly diagnosed whether or not a lesion was a CPAM in 75% of cases (sensitivity 93%, specificity 32%). Fetal MRI had a similar concordance rate (73%) but was superior in correctly determining whether a systemic feeding vessel was present in 80% of cases (sensitivity 71%, specificity 88%) compared with an ultrasound accuracy rate of 72% (sensitivity 49%, specificity 93%). By comparison, postnatal CT correctly diagnosed whether a CPAM was present in 84% of cases (sensitivity 86%, specificity 77%) and whether a systemic feeding vessel was present in 90% of cases (sensitivity 92%, specificity 88%).

Conclusions: Fetal ultrasound remains an important tool in the detection and evaluation of congenital lung malformations. However, it does not correctly predict histology in approximately 25% of prenatally detected CLMs and remains limited by relatively poor sensitivity for systemic feeding vessels pathognomic for a bronchopulmonary sequestration. These data suggest the importance of obtaining additional cross-sectional imaging, preferably a postnatal CT scan, in all patients to help counsel families and to guide in the optimal management of these lesions.

Keywords: fetal medicine; lung; paediatric surgery.

MeSH terms

  • Cystic Adenomatoid Malformation of Lung, Congenital / diagnostic imaging
  • Female
  • Humans
  • Lung / abnormalities*
  • Lung / diagnostic imaging*
  • Lung / embryology
  • Lung Diseases / congenital*
  • Magnetic Resonance Imaging / methods
  • Pregnancy
  • Prenatal Diagnosis / methods*
  • Respiratory System Abnormalities / diagnostic imaging*