Budd-Chiari syndrome: treatment with percutaneous transhepatic recanalization and dilation
J F Lois1, S Hartzman, C T McGlade
1Department of Radiological Sciences, UCLA School of Medicine 90024.
Insights
This study details a child with Budd-Chiari syndrome, successfully treated with percutaneous recanalization and dilation of hepatic vein obstruction and inferior vena cava web. The intervention led to rapid symptom improvement and normalized prothrombin time.
Area of Science:
- Vascular Surgery
- Pediatric Gastroenterology
- Interventional Radiology
Background:
- Budd-Chiari syndrome in children is rare and often linked to venous obstruction.
- Membranous obstruction of hepatic veins and inferior vena cava webs are specific etiologies.
- Timely diagnosis and intervention are crucial for managing pediatric Budd-Chiari syndrome.
Observation:
- A pediatric patient presented with Budd-Chiari syndrome.
- Imaging revealed membranous obstruction of hepatic veins and an inferior vena cava web.
- Clinical manifestations included hepatomegaly and ascites.
Findings:
- Transhepatic catheter venography confirmed the venous occlusive disease.
- Percutaneous transhepatic recanalization and balloon dilation were performed.
- Successful recanalization of the hepatic veins and inferior vena cava was achieved.
Implications:
- Percutaneous intervention offers a minimally invasive treatment option for pediatric Budd-Chiari syndrome.
- Successful recanalization can rapidly alleviate symptoms like hepatomegaly and ascites.
- This approach can normalize coagulation parameters, improving patient outcomes.
Abstract:
The authors describe a child with Budd-Chiari syndrome secondary to membranous obstruction of the hepatic veins and a web in the inferior vena cava. Transhepatic catheter venography demonstrated the occlusion, which was recanalized and dilated percutaneously via a transhepatic approach. Hepatomegaly and ascites decreased promptly and the prothrombin time became normal.
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