Eur J Pediatr Surg 2013; 23(01): 053-056
DOI: 10.1055/s-0033-1333890
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Congenital Lung Lesions: Preoperative Three-Dimensional Reconstructed CT Scan as the Definitive Investigation and Surgical Management

Atif Saeed
1   Department of Paediatric Surgery, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
,
Marcin Kazmierski
1   Department of Paediatric Surgery, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
,
Abdul Khan
1   Department of Paediatric Surgery, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
,
Donna McShane
2   Department of Respiratory and General Paediatrics, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
,
Anna Gomez
3   Department of Radiology, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
,
Adil Aslam
1   Department of Paediatric Surgery, Addenbrooke's Hospital Cambridge, Cambridge, United Kingdom
› Author Affiliations
Further Information

Publication History

18 May 2012

03 January 2013

Publication Date:
02 February 2013 (online)

Abstract

Aim of Study The aim of this study was to review our experience of postnatal investigations and management of congenital lung lesions.

Methods All children with antenatal diagnosis undergoing surgical management were identified from hospital records. Antenatal diagnosis and serial antenatal ultrasound findings were noted, postnatal chest X-ray (CXR) and computed tomographic (CT) scan were reviewed. Pearson correlation coefficient (r) was used to look into relation between CT scan and per-operative findings. Surgical management and outcome of these lesions were assessed.

Results A total of 38 children were identified between January 2000 and December 2011; 22 were males and 16 were females. The mean gestational age at diagnosis was 21 weeks (range18 to 26 weeks). Five children showed complete resolution antenatally. Four children were symptomatic at birth. Postnatal CXR showed an abnormality in only 17 infants. CT scan with three-dimensional (3D) reconstructions was performed at the mean age of 7.7 months (range 1 day to 42 months). CT scan correlated well with per-operative findings and provided adequate anatomical information r = 0.98. Open thoracotomy and lobectomy/excision was performed in 23, and 15 had thoracoscopic lobectomy/excision. The mean age of operation was 18 months (range 2 days to 96 months). Twenty patients had signs of recurrent preoperative infection with pleural adhesions and hilar thickening resulting in conversion of 10 thoracoscopic cases to open surgery. Histology confirmed 26 congenital cystic adenomatoid malformations, 2 hybrid lesions, 7 sequestrations, and 3 bronchopulmonary malformations.

Conclusions Antenatal resolution and normal postnatal CXR are not reliable indicators of resolution of the lesion. Early postnatal CT scan preferably with 3D reconstruction and early surgical treatment are suggested, as delaying the operation may result in repeated infection making thoracoscopic approach more difficult.

 
  • References

  • 1 Davenport M, Warne SA, Cacciaguerra S, Patel S, Greenough A, Nicolaides K. Current outcome of antenally diagnosed cystic lung disease. J Pediatr Surg 2004; 39 (4) 549-556
  • 2 Illanes S, Hunter A, Evans M, Cusick E, Soothill P. Prenatal diagnosis of echogenic lung: evolution and outcome. Ultrasound Obstet Gynecol 2005; 26 (2) 145-149
  • 3 Williams HJ, Johnson KJ. Imaging of congenital cystic lung lesions. Paediatr Respir Rev 2002; 3 (2) 120-127
  • 4 Nasr A, Himidan S, Pastor AC, Taylor G, Kim PC. Is congenital cystic adenomatoid malformation a premalignant lesion for pleuropulmonary blastoma?. J Pediatr Surg 2010; 45 (6) 1086-1089
  • 5 Oliveira C, Himidan S, Pastor AC , et al. Discriminating preoperative features of pleuropulmonary blastomas (PPB) from congenital cystic adenomatoid malformations (CCAM): a retrospective, age-matched study. Eur J Pediatr Surg 2011; 21 (1) 2-7
  • 6 Eber E. Antenatal diagnosis of congenital thoracic malformations: early surgery, late surgery, or no surgery?. Semin Respir Crit Care Med 2007; 28 (3) 355-366
  • 7 Sauvat F, Michel JL, Benachi A, Emond S, Revillon Y. Management of asymptomatic neonatal cystic adenomatoid malformations. J Pediatr Surg 2003; 38 (4) 548-552
  • 8 Oh BJ, Lee JS, Kim JS, Lim CM, Koh Y. Congenital cystic adenomatoid malformation of the lung in adults: clinical and CT evaluation of seven patients. Respirology 2006; 11 (4) 496-501
  • 9 van Leeuwen K, Teitelbaum DH, Hirschl RB , et al. Prenatal diagnosis of congenital cystic adenomatoid malformation and its postnatal presentation, surgical indications, and natural history. J Pediatr Surg 1999; 34 (5) 794-798 , discussion 798–799
  • 10 Lee EY, Tracy DA, Mahmood SA, Weldon CB, Zurakowski D, Boiselle PM. Preoperative MDCT evaluation of congenital lung anomalies in children: comparison of axial, multiplanar, and 3D images. AJR Am J Roentgenol 2011; 196 (5) 1040-1046
  • 11 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) 329-334 , discussion 329–334
  • 12 Brenner D, Elliston C, Hall E, Berdon W. Estimated risks of radiation-induced fatal cancer from pediatric CT. AJR Am J Roentgenol 2001; 176 (2) 289-296
  • 13 Murphy JJ, Blair GK, Fraser GC , et al. Rhabdomyosarcoma arising within congenital pulmonary cysts: report of three cases. J Pediatr Surg 1992; 27 (10) 1364-1367
  • 14 Kim YT, Kim JS, Park JD, Kang CH, Sung SW, Kim JH. Treatment of congenital cystic adenomatoid malformation-does resection in the early postnatal period increase surgical risk?. Eur J Cardiothorac Surg 2005; 27 (4) 658-661
  • 15 Marshall KW, Blane CE, Teitelbaum DH, van Leeuwen K. Congenital cystic adenomatoid malformation: impact of prenatal diagnosis and changing strategies in the treatment of the asymptomatic patient. AJR Am J Roentgenol 2000; 175 (6) 1551-1554