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Percutaneous transhepatic occlusion for bleeding oesophageal varices in polycystic disease
Archives of Disease in Childhood
|December 1, 1981
Insights
Percutaneous transhepatic varix embolization successfully treated portal hypertension in a child with congenital polycystic kidney and liver disease. This minimally invasive procedure prevented further gastrointestinal bleeding episodes.
Area of Science:
- Pediatric Gastroenterology
- Interventional Radiology
- Hepatology
Background:
- Congenital polycystic kidney and liver disease can lead to serious complications like portal hypertension.
- Portal hypertension in pediatric patients often results in gastro-oesophageal varices, increasing the risk of upper gastrointestinal bleeding.
Observation:
- A 7-year-old boy diagnosed with congenital polycystic disease of the kidneys and liver presented with significant portal hypertension.
- The patient experienced two episodes of upper gastrointestinal bleeding due to gastro-oesophageal varices.
Findings:
- Percutaneous transhepatic occlusion of varices and the left gastric vein was performed as an intervention.
- Following the procedure, the patient remained free of further haemorrhage for one year.
Implications:
- Percutaneous transhepatic varix embolization is a viable and effective treatment for managing gastrointestinal bleeding in pediatric patients with congenital polycystic disease.
- This interventional approach offers a minimally invasive alternative for controlling variceal bleeding in complex pediatric cases.
- Successful embolization can significantly improve patient outcomes by preventing recurrent bleeding and associated morbidity.
Abstract:
A 7-year-old boy with congenital polycystic disease of the kidneys and liver developed portal hypertension and gastro-oesophageal varices. After two episodes of upper gastrointestinal bleeding, percutaneous transhepatic occlusion of varices and of the left gastric vein was carried out. During the next year there was no evidence of further haemorrhage.