medigraphic.com
Órgano Oficial del Instituto Nacional de Pediatría

2010, Number 2

<< Back Next >>

Acta Pediatr Mex 2010; 31 (2)

Congenital pulmonary airway malformation. Report of a case and review of the literature

Palmer-Becerra JD, Montalvo- Marín A, Uro-Huerta H, Gutiérrez- Lucatero S, Madriñan-Rivas JE

Language: Spanish
References: 15
Page: 70-74
PDF size: 556.56 Kb.


ABSTRACT

Congenital pulmonary airway malformation is a rare condition characterized by the presence of an abnormal mass of immature malformed tissue with varying degrees of cystic changes. It is diagnosed prenatally by ultrasound scan. Postnatal presentation ranges from severe respiratory distress with neonatal death to asymptomatic lesions. Thoracoscopic surgical resection has shown to be safe and associated with a lower incidence of postoperative complications.


REFERENCES

  1. Stocker JT. Congenital pulmonary airway malformation: a new name for an expanded classification of congenital cystic adenomatoid malformation of the lung. Histopathology. 2002; 41(supplement 2): 424-30.

  2. Rodgers BM, Harman PK, Johnson AM. Bronchopulmonary foregut malformations. Ann Surg. 1986;203:517-24.

  3. Black TL. Pulmonary sequestration and congenital cystic adenomatoid malformations. In: Ziegler MM, Azizkhan RG, Weber TR (eds): Operative pediatric surgery. Philadelphia: W.B. McGraw-Hill; 2003.

  4. Sadler TW. Embriología médica con orientación clínica. 9a. edición. Buenos Aires: Médica Panamericana; 2004. p. 289- 99.

  5. Wang NS, Chen MF, Chen FF. The glandular component in congenital cyst adenomatoid malformation of the lung. Respirology. 1999;4:147-53.

  6. Stocker JT. The respiratory tract. In: Stocker JT, Dehner LP. Pediatric pathology. 2nd ed. Philadelphia: Lippincott W&W; 2002. p. 445-517.

  7. Adzick NS, Farmer DL. Cysts of the lungs and mediastinum. In: Grosfeld JL, O´Neill JA, Fonkalsrud EW, Coran AG. Pediatric surgery. 6th ed. St. Louis: Mosby; 2006. p. 955-70.

  8. Vu L, Tsao K, Lee H, Nobuhara K, Farmer D, Harrison M, Goldstein R. Characteristics of congenital cystic adenomatoid malformations associated with nonimmune hydrops and outcome. J Pediatr Surg. 2007;42:1351-6.

  9. Smith M, Samuel M, Lees C, Set P, D´Amore A. Congenital pulmonary malformations associated with esophageal duplication and teratoma: prenatal to postnatal management. J Pediatr Surg. 2008;43:E31-E33.

  10. Morris LM, Lim FY, Livingston JC, Polzin WJ, Crombleholme TM. High risk fetal congenital pulmonary airway malformations have a variable response to steroids. J Pediatr Surg. 2009;44:60-65.

  11. Grethel EJ, Wagner AJ, Clifton MS, et al. Fetal intervention for mass lesions and hydrops improves outcome: a 15-years experience. J Pediatr Surg. 2007;42:117-23.

  12. Aziz D, Langer JC, Tuuha SE, Ryan G, Ein SH, Kim PC. Perinatally diagnosed asymptomatic congenital cystic adenomatoid malformation: to resect or not? J Pediatr Surg. 2004;39(3):329- 34.

  13. Truitt AK, Carr SR, Cassese J, Kurkchubasce AG, Tracy TF, Luks FI. Perinatal management of congenital cystic lung lesions in the age of minimally invasive surgery. J Pediatr Surg. 2006;41:893-96.

  14. Vu LT, Farmer DL, Nobuhara KK, Miniati D, Lee H. Thoracoscopic versus open resection for congenital cystic adenomatoidmalformation of the lung. J Pediatr Surg. 2008;43:35-39.

  15. Phaloprakarn C, Pott EM, Harrison MR. Residual congenital cystic adenomatoid malformation and thoracic scar deformation after fetal surgery: a case report. J Pediatr Surg. 2006;41:E11-E14.




2020     |     www.medigraphic.com