Chylopericardium in a child with impaired venous access following small bowel transplantation

V Bhole1, S Gozzini, O Stumper

  • 1Cardiology Unit, Birmingham Children's Hospital, Birmingham, UK.

Pediatric Transplantation
|October 22, 2009
PubMed

Insights

A child with impaired venous access after a small bowel transplant developed chylopericardium. Treatment involved pericardiocentesis and a specialized diet, with venous occlusion identified as the likely cause.

Area of Science:

  • Pediatric surgery
  • Gastroenterology
  • Cardiology

Background:

  • A 10-year-old child with complex venous access issues (occluded jugular, subclavian, and innominate veins) underwent an isolated small bowel transplant.
  • Post-transplant follow-up revealed the development of chylopericardium, presenting as lethargy and shortness of breath.

Observation:

  • Diagnostic imaging, including MR venography and lymphangiography, failed to pinpoint the exact site of the lymphatic leak.
  • The patient's chylopericardium was managed through pericardiocentesis and a medium-chain triglyceride (MCT) diet.

Findings:

  • The primary finding suggests that venous occlusion in the subclavian veins, leading to increased backpressure, was the most probable cause of the lymphatic leak and subsequent chylopericardium.
  • This case highlights a rare complication following intestinal transplantation in a pediatric patient with pre-existing venous anomalies.

Implications:

  • Understanding the link between venous occlusion and lymphatic leaks is crucial for managing post-transplant complications.
  • This case underscores the importance of considering venous hypertension in the etiology of chylopericardium in immunocompromised patients.
  • Further research into diagnostic and therapeutic strategies for chylopericardium secondary to venous issues post-transplant is warranted.

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