Successful thoracic duct embolisation in a child with recurrent massive pericardial effusion diagnosed as a lymphatic
Jue Seong Lee1, Mi Kyoung Song2, Saebeom Hur3
1Department of Pediatrics, Korea University College of Medicine and Korea University Medical Center, Seoul, South Korea.
Insights
A rare case of massive pericardial effusion in a child was diagnosed using magnetic resonance lymphangiography. Percutaneous embolisation of the thoracic duct successfully treated this lymphatic abnormality.
Area of Science:
- Cardiology
- Radiology
- Pediatrics
Background:
- Idiopathic massive pericardial effusion is rare in children.
- Pulmonary lymphangiectasia can be associated with lymphatic abnormalities.
Observation:
- A 29-month-old girl presented with chronic, recurrent massive pericardial effusion.
- CT imaging suggested pulmonary lymphangiectasia, prompting further investigation.
- Magnetic resonance lymphangiography revealed thoracic duct dilation and chylolymphatic reflux into the pericardial space.
Findings:
- The condition was diagnosed as primary chylopericardium with lymphangiectasia.
- Initial thoracic duct embolisation led to immediate resolution of pericardial effusion.
- Recurrence was successfully treated with additional embolisation of collateral lymphatic vessels.
Implications:
- Magnetic resonance lymphangiography is a valuable tool for diagnosing complex lymphatic disorders.
- Percutaneous embolisation offers a minimally invasive treatment option for chylopericardium.
- This case highlights the importance of considering lymphatic abnormalities in pediatric pericardial effusion.
Abstract:
A 29-month-old girl had idiopathic massive pericardial effusion for over 6 months. Lymphangiography was performed for chronic and recurrent pericardial effusion and pulmonary lymphangiectasia, suspected based on CT findings. Magnetic resonance lymphangiography revealed chylolymphatic reflux from a tortuously dilated thoracic duct in the mediastinum to the pericardial space, suggesting primary chylopericardium with lymphangiectasia. Pericardial effusion resolved immediately after thoracic duct embolisation at the lower thoracic level. However, pericardial effusion recurred after 5 months, which resolved after additional embolisation of the abnormal lymphatic collateral vessels from the remnant upper thoracic duct. Here, we report an unusual case with chylous massive pericardial effusion diagnosed by magnetic resonance lymphangiography and treated with percutaneous embolisation.
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