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January 23, 2026Journal of Surgical Case Reports0 citationsOpen Access

Complex case of congenital pulmonary sequestration with successful “EXIT” procedure

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RBRūta BernatavičienėVilnius University Hospital Santariskiu KlinikosGPGabija PikturnaitėVilnius UniversityGVGilvydas VerkauskasCEA LITEN

Key Points

  • To report a case of congenital extralobar pulmonary sequestration and demonstrate the efficacy of the EXIT procedure.
  • Case report involving a 22-year-old primigravida at 29 weeks gestation.
  • Used magnetic resonance imaging to confirm diagnosis of pulmonary sequestration.
  • Applied the EXIT procedure during Cesarean section to facilitate neonatal breathing.
  • Newborn required intensive care for respiratory distress, heart failure, and pulmonary hypertension.
  • Patient discharged stable after 3 weeks postnatally.
  • Elective thoracoscopy at 6 months successfully removed the sequestration without complications.

Abstract

Abstract The ex-utero intrapartum treatment (EXIT) procedure preserves fetal oxygenation via the umbilical cord in urgent respiratory distress. We report a rare case of congenital extralobar pulmonary sequestration with pedicle torsion. A 22-year-old primigravida at 29 + 4 weeks presented with a fetal supradiaphragmatic mass, hydrothorax, and cardiac displacement; fetal magnetic resonance imaging (MRI) confirmed pulmonary sequestration. Rapid fetal deterioration led to the termination of the pregnancy and the application of ex-utero intrapartum treatment procedure during Cesarean section. Before cord clamping, intubation along with thoracocentesis enabled neonatal breathing. The 2140 g newborn required intensive care for respiratory distress, heart failure, and pulmonary hypertension and was discharged stable after 3 weeks. Elective thoracoscopy at the age of 6 months removed the sequestration, confirming pedicle torsion; recovery was uneventful. This case highlights the importance of early diagnosis, multidisciplinary collaboration, and timely use of ex-utero intrapartum treatment to manage life-threatening fetal lung anomalies.

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Cite This Study

Bernatavičienė et al. (2025) studied this question.

synapsesocial.com/papers/69731047c8125b09b0d1ff9bhttps://doi.org/10.1093/jscr/rjaf1066
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