SciELO - Scientific Electronic Library Online

 
vol.32 issue3Nijmegen breakage syndrome: The importance of follow-upAquagenic palmoplantar keratoderma associated with cystic fibrosis gene mutation author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Nascer e Crescer

Print version ISSN 0872-0754On-line version ISSN 2183-9417

Abstract

ANTUNES, Joana et al. Congenital chylothorax: A series of eight cases. Nascer e Crescer [online]. 2023, vol.32, n.3, pp.217-223.  Epub Sep 30, 2023. ISSN 0872-0754.  https://doi.org/10.25753/birthgrowthmj.v32.i3.25442.

Introduction:

Congenital chylothorax (CC) is the accumulation of lymph in the pleural space. The aim of this study was to review the cases of CC diagnosed in newborns admitted to a level III neonatal intensive care unit between January 2014 and December 2020.

Results:

Eight cases of CC were identified, all with prenatal diagnosis. After postnatal confirmation of the diagnosis, supportive care and conservative therapy were initiated. Six cases underwent mechanical ventilation, two were treated with surfactant and inhaled nitric oxide, four required inotropic support, and one underwent extracorporeal membrane oxygenation. Five newborns were effectively treated with octreotide. One patient with hydrops fetalis died after birth.

Discussion:

The prognosis of CC depends on the severity of the effusion and on associated abnormalities. Medical treatment is based on supportive and conservative treatment. Although the use of octreotide is not unanimous, it proved to be an effective and safe adjuvant therapy in these patients.

Keywords : chylothorax; congenital abnormality; hydrops fetalis; neonatal; octreotide; pleural effusion.

        · abstract in Portuguese     · text in English     · English ( pdf )