Computer-aided quantitative MSCT measurements may be useful for congenital lung malformations surgical approach selection
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology, and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00383-021-04949-4.pdf
Reference24 articles.
1. Hall NJ, Stanton MP (2017) Long-term outcomes of congenital lung malformations. Semin Pediatr Surg 26:311–316. https://doi.org/10.1053/j.sempedsurg.2017.09.001
2. Wong K, Flake AW, Tibboel D, Rottier RJ, Tam P (2018) Congenital pulmonary airway malformation: advances and controversies. Lancet Child Adolesc Health 2:290–297. https://doi.org/10.1016/S2352-4642(18)30035-X
3. Criss CN, Musili N, Matusko N, Baker S, Geiger JD, Kunisaki SM (2018) Asymptomatic congenital lung malformations: is nonoperative management a viable alternative? J Pediatr Surg 53:1092–1097. https://doi.org/10.1016/j.jpedsurg.2018.02.065
4. Laberge JM, Flageole H, Pugash D, Khalife S, Blair G, Filiatrault D et al (2001) Outcome of the prenatally diagnosed congenital cystic adenomatoid lung malformation: a Canadian experience. Fetal Diagn Ther 16:178–186. https://doi.org/10.1159/000053905
5. Lima JS, Camargos PA, Aguiar RA, Campos AS, Aguiar MJ (2014) Pre and perinatal aspects of congenital cystic adenomatoid malformation of the lung. J Matern Fetal Neonatal Med 27:228–232. https://doi.org/10.3109/14767058.2013.807236
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