Complex congenital lung malformation resection by uniportal VATS-case report.
Détails
Télécharger: 35070259_BIB_C7BC33E47FAB.pdf (268.02 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_C7BC33E47FAB
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Complex congenital lung malformation resection by uniportal VATS-case report.
Périodique
Journal of surgical case reports
ISSN
2042-8812 (Print)
ISSN-L
2042-8812
Statut éditorial
Publié
Date de publication
04/2021
Peer-reviewed
Oui
Volume
2021
Numéro
4
Pages
rjab069
Langue
anglais
Notes
Publication types: Case Reports
Publication Status: epublish
Publication Status: epublish
Résumé
Bronchial atresia (BA) is a rare congenital pulmonary airway malformation. It is characterized by the focal stenosis of a proximal segmental bronchus associated with peripheral mucus impaction and hyperinflation of the obstructed lung segment. Most cases are identified during neonatal period or childhood. When diagnosed in adults, BA may present with recurrent infections, pneumothorax and destruction of affected parenchyma. Thoracoscopic approach to BA has proved challenging in adult patients because of repeated infections and subsequently, its inflammatory status. Herein we present a case of a 26-year-old female with left side recurrent pneumonia and pneumothorax past history. A chest computed tomography revealed a complex congenital bronchial atresia involving the left upper lobe and basal segments, associated to vascular anomalies. She underwent a successful uniportal VATS left upper lobectomy and resection of basal segments. Uniportal VATS approach is an effective and safe treatment for the management of complex congenital lung malformation.
Mots-clé
Surgery
Pubmed
Web of science
Open Access
Oui
Création de la notice
03/09/2021 19:55
Dernière modification de la notice
08/08/2024 6:40