SciELO - Scientific Electronic Library Online

 
vol.32 número3Síndrome de quebras de Nijmegen: A importância do seguimentoAcroqueratodermia aquagénica associada a mutação do gene da fibrose quística índice de autoresíndice de assuntosPesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Nascer e Crescer

versão impressa ISSN 0872-0754versão On-line ISSN 2183-9417

Resumo

ANTUNES, Joana et al. Congenital chylothorax: A series of eight cases. Nascer e Crescer [online]. 2023, vol.32, n.3, pp.217-223.  Epub 30-Set-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.

Palavras-chave : chylothorax; congenital abnormality; hydrops fetalis; neonatal; octreotide; pleural effusion.

        · resumo em Português     · texto em Inglês     · Inglês ( pdf )