Abstract
Congenital lung lesions vary in their histological patterns but often have a similar clinical presentation, namely, respiratory difficulties and recurrent infections. Routine prenatal imaging has led to an increase in diagnosis in the fetal period. The fetal lung lesions grow rapidly between 20 and 26 weeks’ gestation after which most will regress. Some of these lesions exhibit a mass effect that compresses normal lung tissue, leading to pulmonary hypoplasia, or compression of the heart and mediastinal structures, leading to hydrops and fetal demise. Options for fetal intervention include decompression of large cystic masses, open fetal surgery, and ex utero intrapartum treatment. More recently administration of maternal corticosteroids has been employed to decrease the growth of the fetal lung mass, but blinded randomized controlled trials are needed to prove efficacy. Symptomatic neonates require surgical resection. Asymptomatic neonates can be followed with chest CT, no earlier than 6 weeks of life, to further characterize the lesions. Small asymptomatic lesions may be observed if there is no concern for pleuropulmonary blastoma, a malignancy sometimes seen even in newborns. Resection is indicated to avoid infection or future symptoms and is frequently done thoracoscopically. Outcomes are generally excellent.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsSuggested Reading
Baird R, Puligandla PS, Laberge JM. Congenital lung malformations: informing best practice. Semin Pediatr Surg. 2014;23(5):270–7.
Cass DL, Olutoye OO, Cassady CI, Moise KJ, Johnson A, Papanna R, et al. Prenatal diagnosis and outcome of fetal lung masses. J Pediatr Surg. 2011;46(2):292–8.
Cass DL, Olutoye OO, Cassady CI, Zamora IJ, Ivey RT, Ayres NA, et al. EXIT-to-resection for fetuses with large lung masses and persistent mediastinal compression near birth. J Pediatr Surg. 2013;48(1):138–44.
Crombleholme TM, Coleman B, Hedrick H, Liechty K, Howell L, Flake AW, et al. Cystic adenomatoid malformation volume ratio predicts outcome in prenatally diagnosed cystic adenomatoid malformation of the lung. J Pediatr Surg. 2002;37(3):331–8.
Curran PF, Jelin EB, Rand L, Hirose S, Feldstein VA, Goldstein RB, et al. Prenatal steroids for microcystic congenital cystic adenomatoid malformations. J Pediatr Surg. 2010;45(1):145–50.
Tsao K, Hawgood S, Vu L, Hirose S, Sydorak R, Albanese CT, et al. Resolution of hydrops fetalis in congenital cystic adenomatoid malformation after prenatal steroid therapy. J Pediatr Surg. 2003;38(3):508–10. PubMed Epub 2003/03/13. eng.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2017 Springer International Publishing AG
About this chapter
Cite this chapter
Akinkuotu, A.C., Olutoye, O.O. (2017). Congenital Lung Lesions. In: Mattei, P., Nichol, P., Rollins, II, M., Muratore, C. (eds) Fundamentals of Pediatric Surgery. Springer, Cham. https://doi.org/10.1007/978-3-319-27443-0_38
Download citation
DOI: https://doi.org/10.1007/978-3-319-27443-0_38
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-27441-6
Online ISBN: 978-3-319-27443-0
eBook Packages: MedicineMedicine (R0)