[an error occurred while processing this directive]

Advanced Ultrasound in Diagnosis and Therapy ›› 2018, Vol. 2 ›› Issue (2): 133-138.doi: 10.37015/AUDT.2018.180812

• • 上一篇    下一篇

  

  • 收稿日期:2018-07-01 出版日期:2018-08-18 发布日期:2018-08-19

Sonographic Characteristics of Congenital Pulmonary Airway Malformations in Children: A Report of 21 Cases and Review of Literature

Hongkui Yu, MDa, Zhihui Li, MDa, Xiao Liu, MDa, Weiling Chen, MDa, Yuanxiang Wang, MDb, Bei Xia, MDa,*()   

  1. a Department of Ultrasonography, Shenzhen Children’s Hospital, Shenzhen, China
    b Department of Cardiothoracic Surgery, Shenzhen Children’s Hospital, Shenzhen, China
  • Received:2018-07-01 Online:2018-08-18 Published:2018-08-19
  • Contact: Bei Xia, MD E-mail:xiabeimd@gmail.com

Abstract:

Objective: This study discusses the diagnostic value of ultrasonography for congenital pulmonary airway malformations (CPAM) in children.
Methods: A retrospective analysis was conducted for 21 pathologically confirmed paediatric cases of CPAM by reviewing the ultrasonography images and comparing them with the clinical and pathologic results.
Results: All 21 paediatric cases of CPAM had lesions in unilateral lobes, with five cases involving the left lung and 16 cases involving the right lung. There were six cases with type 1 ultrasonography manifestations, 12 cases with type 2 ultrasonography manifestations and one case with a type 4 ultrasonography manifestation. One case was misdiagnosed as pulmonary sequestration (PS) by ultrasonography, and another case had no abnormalities based on ultrasonography. With respect to the pathologic results, six type 1 (28.6%), 13 type 2 (61.9%) and one type 4 (4.8%) were found, and one type 2 was complicated with PS (4.8%). The ultrasonography diagnoses agreed with surgical pathology reports in 18 cases (85.7%).
Conclusion: Ultrasonography is feasible and accurate in identifying subtype within postnatally diagnosed pediatric CPAM lesions.

Key words: Lung, Congenital abnormalities, Child, Ultrasonography, Diagnosis

[1] Lantuejoul S, Nicholson AG, Sartori G, Piolat C, Danel C, Brabencova E, et al. Mucinous cells in type 1 pulmonary congenital cystic adenomatoid malformation as mucinous bronchioloalveolar carcinoma precursors. Am J Surg Pathol 2007; 31:961-9.
[2] McDonough RJ, Niven AS, Havenstrite KA. Congenital pulmonary airway malformation: a case report and review of the literature. Respir Care 2012; 57:302-6.
[3] Beydon N, Larroquet M, Coulomb A. Comparison between US and MRI in the prenatal assessment of lung malformations. Pediatr Radiol 2013; 43:685-96.
[4] Mann S1, Wilson RD, Bebbington MW, Adzick NS, Johnson MP. Antenatal diagnosis and management of congenital cystic adenomatoid malformation. Semin Fetal Neonatal Med 2007; 12:477-81.
[5] Stocker JT. Congenital pulmonary airway malformation: A new name and an expanded classification of congenital cystic adenomatoid malformation of the lung. Histopathol 2002; 41:424-31.
[6] Chikkannaiah P, Kangle R, Hawal M. Congenital cystic adenomatoid malformation of lung: Report of two cases with review of literature. Lung India 2013; 30:215-8.
[7] Stocker JT, Madewell JE, Drake RM. Congenital cystic adenomatoid malformation of the lung. Classification and morphologic spectrum. Hum Pathol 1977; 8:155-71.
[8] Bolde S, Pudale S, Pandit G, Ruikar K, Ingle SB. Congenital pulmonary airway malformation: A report of two cases. World J Clin Cases 2015; 3:470-3.
[9] Monni G, Paladini D, Ibba RM, Teodoro A, Zoppi MA, Lamberti A, et al. Prenatal ultrasound diagnosis of congenital cystic adenomatoid malformation of the lung: a report of 26 cases and review of the literature. Ultrasound Obstet Gynecol 2000; 16:159-62.
[10] McLean SE, Pfeifer JD, Siegel MJ, Jensen ER, Schuler PM, Hirsch R, et al. Congenital cystic adenomatoid malformation connected to an extralobar pulmonary sequestration in the contralateral chest: common origin? J Pediatr Surg 2004; 39:e13-7.
[11] Kravitz RM. Congenital malformations of the lung. Pediatr Clin North Am 1994; 41:453-72.
[12] Kwon YS, Koh WJ, Han J, Choi YS, Kim K, Kim J, et al. Clinical characteristics and feasibility of thoracoscopic approach for congenital cystic adenomatoid malformation in adults. Eur J Car-diothorac Surg 2007; 31:797-801.
[13] Wong A, Vieten D, Singh S, Harvey JG, Holland AJ. Long-term outcome of asymptomatic patients with congenital cystic adenomatoid malformation. Pediatr Surg Int 2009; 25:479-85.
[14] Naito Y, Beres A, Lapidus-Krol E, Lembo MA, Zennaro F, Bussani R, et al. Does earlier lobectomy result in better long-term pulmonary function in children with congenital lung anomalis ? A prospective study. J Pediatr Surg 2012; 47:852-6.
[15] Pelizzo G, Barbi E, Codrich D, Lembo MA, Zennaro F, Bussani R, et al. Chronic inflammation in congenital cystic adenomatoid malformations.An underestimated risk factor? J Pediatr Surg 2009; 44:616-9.
[16] Laberge JM, Puligandla P, Flageole H. Asymptomatic congenital lung malformations. Semin Pediatr Surg 2005; 14:16-33.
[17] Chowdhury MM, Chakraborty S. Imaging of congenital lung malformations. Semin Pediatr Surg 2015; 24:168-75.
No related articles found!
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!
[an error occurred while processing this directive]