In utero congenital chylothorax treatment with fetal thoracoamniotic shunt: Case report

D. M. Hannah, M. L. Badell, P. C. Woodham

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)427-430
Number of pages4
JournalJournal of Neonatal-Perinatal Medicine
Volume13
Issue number3
DOIs
StatePublished - 2020
Externally publishedYes

Keywords

  • Fetal thoracoamniotic shunt
  • congenital chylothorax
  • fetal hydrothorax
  • fetal pleural effusion

ASJC Scopus subject areas

  • General Medicine

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