Surgical treatment of pulmonary sequestration in adults and children: long-term results.
Adolescent
Adult
Aged
Bronchopulmonary Sequestration
/ diagnosis
Child
Child, Preschool
Female
Humans
Incidence
Infant
Infant, Newborn
Italy
/ epidemiology
Male
Middle Aged
Postoperative Complications
/ epidemiology
Retrospective Studies
Thoracic Surgery, Video-Assisted
/ methods
Tomography, X-Ray Computed
/ methods
Treatment Outcome
Young Adult
Lung surgery
Paediatric surgery
Pulmonary sequestration
Journal
Interactive cardiovascular and thoracic surgery
ISSN: 1569-9285
Titre abrégé: Interact Cardiovasc Thorac Surg
Pays: England
ID NLM: 101158399
Informations de publication
Date de publication:
01 07 2020
01 07 2020
Historique:
received:
23
09
2019
revised:
11
01
2020
accepted:
30
01
2020
pubmed:
18
4
2020
medline:
2
2
2021
entrez:
18
4
2020
Statut:
ppublish
Résumé
Few experiences comparing paediatric and adult patients treated for pulmonary sequestration (PS) have been reported. Surgical treatment is considered the best choice, but the time of surgery is still controversial. We present our experience in this setting, comparing characteristics, histological results and outcome of paediatric and adult patients undergoing PS resection. Between 1998 and 2017, a total of 74 patients underwent lobectomy or sublobar resection for PS. Sixty patients were children (group A: ≤16 years old) and 14 were adults (group B: >16 years old). Preoperative diagnosis was radiological. PS was intralobar (42 cases) and extralobar (32 cases). The operation was a muscle-sparing lateral thoracotomy or video-assisted thoracoscopic surgery. Preoperative characteristics, histological results and short-/long-term results of the 2 groups were retrospectively analysed and compared. Thirty-seven percent of the patients in group A presented with respiratory symptoms and 79% in group B (P = 0.44). Most symptomatic patients were treated with a lobectomy. In group A, 2 patients (3%) had a malignant transformation of the lesion. Patients with a prenatal diagnosis treated after the age of 1 year became more symptomatic than those operated on before the age of 1 year (57% vs 23%; P = 0.08). No differences were found in postoperative complications. Long-term stable remission of respiratory symptoms was obtained in 91% of patients in group A and 100% in group B. Adulthood (P = 0.03) and the association with congenital cystic adenomatoid malformation (P = 0.03) were negative prognostic factors for the development of respiratory symptoms. Surgical treatment of PS is safe and feasible. Despite the small number of patients included, study results indicated that an early operation during childhood may prevent the subsequent development of respiratory symptoms. Surgical treatment is also recommended to prevent the rare transformation into malignancy.
Identifiants
pubmed: 32300793
pii: 5821040
doi: 10.1093/icvts/ivaa054
doi:
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
71-77Informations de copyright
© The Author(s) 2020. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.