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BMJ Case Reports 2009; doi:10.1136/bcr.03.2009.1645
  • Unusual association of diseases/symptoms

Recurrent pulmonary and cerebral thromboembolism in an adult patients following incomplete removal of ventriculoatrial shunt for congenital hydrocephalus

  1. Maria Prastaro1,
  2. Antonio Rapacciuolo1,
  3. Elisa di Pietro1,
  4. Claudia Esposito1,
  5. Francesca Esposito1,
  6. Veronica Russolillo2,
  7. Rosa Iodice3,
  8. Giuseppe Orefice3,
  9. Carlo Vosa2,
  10. Massimo Chiariello1
  1. 1
    Federico II University of Naples, Cardiology, Via S. Pansini, 5, Naples, 80131, Italy
  2. 2
    Federico II University of Naples, Cardiac Surgery, Via S. Pansini, 5, Naples, 80131, Italy
  3. 3
    Federico II University of Naples, Neurology, Via S. Pansini, 5, Naples, 80131, Italy
  1. Antonio Rapacciuolo, rapacciu{at}unina.it
  • Published 19 August 2009

Summary

A 34-year-old man was admitted to our hospital’s department of neurology because he had experienced a cryptogenic stroke followed by a transient ischaemic attack. The patient suffered from congenital hydrocephalus which was treated by ventriculoatrial shunt at 8 months of age. Twelve months later, because of recurrent infections, the catheter was partially removed and the distal segment was left in place. At admission, the transoesophageal echocardiogram showed severe pulmonary hypertension (80 mm Hg confirmed by invasive measurement). The distal tip of the catheter had migrated into the left atrium through a patent foramen ovale inducing a massive right-to-left shunt. We surgically removed the catheter and closed the interatrial defect. At 1 and 6 months follow-up the patient was asymptomatic with a reduced pulmonary hypertension (50 mm Hg). Since there was no other clinical finding responsible for the recurrent thromboembolic events, both at the pulmonary and cerebral level, the catheter was removed to prevent further complications.

Footnotes

  • Competing interests: none.

  • Patient consent: Patient/guardian consent was obtained for publication

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