Literature DB >> 27723920

Antenatally Detected Congenital Pulmonary Airway Malformations: The Oxford Experience.

Hemanshoo Sudhir Thakkar1, Jonathan Durell1, Subhasis Chakraborty2, Bianca-Lea Tingle3, Arnwald Choi3, Darren J Fowler4, Steve J Gould4, Lawrence Impey5, Kokila Lakhoo1.   

Abstract

Congenital airway pulmonary malformations are increasingly being diagnosed, but their management continues to remain controversial. Our approach has been to offer surgery to mitigate the risk of infection and possible malignancy. All patients routinely undergo a CT scan of the chest postnatally and once the diagnosis is confirmed, minimal access surgery is offered. Our anesthetists provide single-lung ventilation to enhance the operative view. We conducted a retrospective review over a 10-year period, during which 91 patients were prenatally suspected to have a cystic lung lesion. There were 88 live births of which 29 (33%) cases were initially managed conservatively based on CT findings. Five of these patients, however, became symptomatic needing surgery. A total of 64 (73%) patients underwent surgery with the most common lesions being congenital pulmonary airway malformations (CPAMs) (24), hybrid lesions (19), and pulmonary sequestrations (12). The median age at surgery was 5 months (1 day to 17 months). Using a minimal access approach, 41 (64%) cases were completed with 17 performed open from the onset. Open surgery was indicated in neonates who became symptomatic within the first few weeks of life as well as patients in respiratory distress that would not tolerate either single-lung ventilation or gas insufflation. There were six further conversions to open from minimal access surgery due to poor visualization or technical difficulties. One patient needed a perioperative blood transfusion and one patient had a more prolonged stay due to persistent air leak managed conservatively. Among asymptomatic patients, evidence of microscopic disease was seen, which included infection as well as two cases of tumors, one pleuropulmonary blastoma seen as part of a CPAM, and one rhabdomyomatous dysplasia seen in the CPAM component of a hybrid lesion. In our experience, excising asymptomatic lesions is safe with minimal complications. Single-lung ventilation in combination with thoracoscopy provides excellent vision. There is a risk of infection and a definite, albeit low, risk of malignancy, which may outweigh the benefits of conservative management. Georg Thieme Verlag KG Stuttgart · New York.

Entities:  

Mesh:

Year:  2016        PMID: 27723920     DOI: 10.1055/s-0036-1593379

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  3 in total

Review 1.  Highlights on MRI of the fetal body.

Authors:  Lucia Manganaro; Amanda Antonelli; Silvia Bernardo; Federica Capozza; Roberta Petrillo; Serena Satta; Valeria Vinci; Matteo Saldari; Francesca Maccioni; Laura Ballesio; Carlo Catalano
Journal:  Radiol Med       Date:  2017-11-21       Impact factor: 3.469

2.  Congenital Cystic Lung Lesions: Redefining the Natural Distribution of Subtypes and Assessing the Risk of Malignancy.

Authors:  Jennifer Pogoriler; Daniel Swarr; Portia Kreiger; N Scott Adzick; William Peranteau
Journal:  Am J Surg Pathol       Date:  2019-01       Impact factor: 6.394

3.  Congenital malformations potentially affecting respiratory function: multidisciplinary approach and follow-up.

Authors:  Valentina Fainardi; Laura Nicoletti; Cristiano Conte; Serena Massa; Lisa Torelli; Alberto Attilio Scarpa; Emilio Casolari; Susanna mariA Roberta Esposito; Giovanna Pisi
Journal:  Acta Biomed       Date:  2020-09-04
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.