Journal of Minimal Access Surgery

ORIGINAL ARTICLE
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Year : 2015  |  Volume : 11  |  Issue : 2  |  Page : 129--133

Congenital pulmonary airway malformation and sequestration: Two standpoints for a single condition

Lucile Fievet1, Claudia Natale2, Xavier-Benoit D'Journo2, Stéphanie Coze3, Jean-Christophe Dubus4, Jean-Michel Guys1, Pascal Thomas2, Pascal De Lagausie1 
1 Department of Paediatric Surgery, Timone and North Children's Hospital, Aix-Marseille University and Assistance Publique-Hôpitaux de Marseille, Marseille, France
2 Thoracic Surgery and Diseases of the Esophagus, North Hospital, Aix-Marseille University and Assistance Publique-Hôpitaux de Marseille, Marseille, France
3 Department of Pediatric and Prenatal Imaging, Timone and North Hospital, Aix-Marseille University and Assistance Publique-Hôpitaux de Marseille, Marseille, France
4 Department of Pediatric Pneumology, Timone and North Children's Hospital, Aix-Marseille University and Assistance Publique-Hôpitaux de Marseille, Marseille, France

Correspondence Address:
Lucile Fievet
Department of Paediatric Surgery, Timone and North Children«SQ»s Hospital, Aix-Marseille University and Assistance Publique-Hôpitaux de Marseille, 264 rue Saint Pierre, 13385 Marseille Cedex 05
France

In adults, congenital pulmonary malformations are candidates for surgery due to symptoms. A pre-natal diagnosis is simple and effective, and allows an early thoracoscopic surgical treatment. A retrospective study was performed to assess management in two different populations of adults and children to define the best strategy. Subjects and Methods: Pulmonary malformations followed at the University Hospital from 2000 to 2012 were reviewed. Clinical history, malformation site, duration of hospitalisation, complications and pathology examinations were collected. Results: A total of 52 cases (33 children, 19 adults) were identified. In children, 28 asymptomatic cases were diagnosed pre-natally and 5 during the neonatal period due to infections. Surgery was performed on the children between the ages of 2 and 6 months. Nineteen adults underwent surgery, 16 because of symptoms and 3 adults for anomalies mimicking tumours. The mean age within the adult group was 42.5 years. In children, there was one thoracotomy and 32 thoracoscopies, with 7 conversions for difficult exposure, dissection of vascular pedicles, bleeding or bronchial injury. In the adults, there were 15 thoracotomies and 4 thoracoscopies, with one conversion. Post-operative complications in the adults were twice as frequent than in children. The mean time of the children«SQ»s hospitalisation was 7.75 days versus 7.16 days for the adults. Pathological examinations showed in the children: 7 sequestrations, 18 congenital cystic pulmonary malformations (CPAM), 8 CPAM associated sequestrations; in adults: 16 sequestrations, 3 intra-pulmonary cysts. Conclusion: Early thoracoscopic surgery allows pulmonary parenchyma conservation with pulmonary development, reduces respiratory and infectious complications, eliminates a false positive cancer diagnosis later in life and decreases risks of thoracic parietal deformation.


How to cite this article:
Fievet L, Natale C, D'Journo XB, Coze S, Dubus JC, Guys JM, Thomas P, De Lagausie P. Congenital pulmonary airway malformation and sequestration: Two standpoints for a single condition.J Min Access Surg 2015;11:129-133


How to cite this URL:
Fievet L, Natale C, D'Journo XB, Coze S, Dubus JC, Guys JM, Thomas P, De Lagausie P. Congenital pulmonary airway malformation and sequestration: Two standpoints for a single condition. J Min Access Surg [serial online] 2015 [cited 2021 Oct 16 ];11:129-133
Available from: https://www.journalofmas.com/article.asp?issn=0972-9941;year=2015;volume=11;issue=2;spage=129;epage=133;aulast=Fievet;type=0