RT Journal Article
SR Electronic
T1 P644 Management of congenital pulmonary malformations: a report on 9 cases
JF Archives of Disease in Childhood
JO Arch Dis Child
FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
SP A407
OP A407
DO 10.1136/archdischild-2019-epa.975
VO 104
IS Suppl 3
A1 Amel Ben Hamed
A1 Chiraz Regaieg
A1 Adel Babay
A1 Manel Charfi
A1 Amira Bouraoui
A1 Nedia Hmida
A1 Ridha Regaieg
A1 Afef Ben Thabet
A1 Abdellatif Gargouri
YR 2019
UL http://adc.bmj.com/content/104/Suppl_3/A407.2.abstract
AB Background Congenital lung malformations (CLMs)) comprise a group of anatomical abnormalities of the respiratory tree. The most common of which include congenital cystic adenomatoid malformation (CAM), bronchopulmonary sequestration (PS), bronchial atresia, congenital lobar emphysema (CLE) and bronchogenic cyst. These anomalies are detected with increasing frequency by pre-natal sonography. When symptomatic, there is little controversy that resection is indicated, which is usually curative. When a lesion is asymptomatic there is greater debate regarding the benefit of resection versus continued observation. The aim of this study is to analyse the management options available and the moyen-term outcomes associated with each treatment option.Methods We enrolled neonates who were admitted to the departement of neonatology at Hedi Chaker hospital, Sfax (Tunisia) within the ten last years and suffered from CLMs.Results Nine cases were reviewed. Among these 8 were boys (88%) and 3 neonates were preterm. The diagnosis was prenatal in 6 cases (66%) and foetal sonography was abnormal in 8 cases (88%). The adaptation to extrauterine life was good in 8 cases (88%). Six infants (66%) were symptomatic when admitted to neonatal unit. Radiological investigations ledeed to the diagnosis in all cases: 5 CAM, 3 PS and CLE in 1 case. Surgery was indicated for three patients . Two were operated before the age of 7 days due to severe clinical symptoms. The other patient was operated at the age of 7 years for possible malignant transformation of a PS. The surgical treatment involved a lobectomy for 2 patients and a thoracoscopy with malformation’s in the other case. The histopathological examinations confirmed the diagnosis in all cases. Except for one patient with CAM, who died a few days after a lobectomy due to acute nosocomial pneumonia, the evolution was good for 8 children with a mean of follow-up of 24 months (10 months to 10 years). Conclusion While the neonatal management of symptomatic CLMs is clear and includes prompt surgery, controversies remain for asymptomatic CPAM due to risk of infections and malignancies.