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In utero congenital chylothorax treatment with fetal thoracoamniotic shunt: Case report.
Hannah, D M; Badell, M L; Woodham, P C.
Afiliação
  • Hannah DM; Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine; The Medical Center Navicent Health, Mercer University School of Medicine, Macon, GA, USA.
  • Badell ML; Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine; Emory University School of Medicine, Atlanta, GA, USA.
  • Woodham PC; Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine; The Medical Center Navicent Health, Mercer University School of Medicine, Macon, GA, USA.
J Neonatal Perinatal Med ; 13(3): 427-430, 2020.
Article em En | MEDLINE | ID: mdl-31744022
ABSTRACT

BACKGROUND:

Fetal pleural effusions are a rare fetal anomaly that may result from congenital chylothorax. Severe cases lead to chest compression with resulting pulmonary hypoplasia and possible neonatal demise. Fetal thoracoamiontic shunt (TAS) placement may decrease the amount of pleural effusion and improve lung expansion. CASE A 30-year-old primigravida at 29 2/7 weeks' gestation presented with fetal bilateral pleural effusions with no identifiable genetic or structural abnormalities. TAS placement accomplished decompression of the left fetal chest. The neonate was delivered at 33 3/7 weeks and required minimal respiratory support with no apparent long term complications at discharge.

CONCLUSION:

This case demonstrated that fetal intervention with TAS placement can improve neonatal outcomes. Referral to an MFM specialist capable of TAS should be considered for isolated fetal bilateral pleural effusion.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derrame Pleural / Quilotórax / Terapias Fetais / Doenças Fetais / Fetoscopia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derrame Pleural / Quilotórax / Terapias Fetais / Doenças Fetais / Fetoscopia Idioma: En Ano de publicação: 2020 Tipo de documento: Article