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Published on: August 8, 2025
[Portal cavernoma in children revealed by gastrointestinal haemorrhage: about a case]
Idrissa Basse1, Ndéye Rama Diagne Guèye1, Dina Cyrienne Obambi Diop1
1Hôpital pour Enfants de Diamniadio, Université de Thiès, Thiès, Sénégal.
Insights
Portal cavernoma, a rare venous vascular anomaly, causes portal hypertension and gastrointestinal bleeding in children. Early diagnosis and treatment are crucial for managing this condition and preventing fatal outcomes.
Area of Science:
- Vascular Surgery
- Pediatric Gastroenterology
- Radiology
Background:
- Portal cavernoma is a venous vascular anomaly resulting from chronic extra-hepatic portal vein occlusion.
- It is a significant cause of portal hypertension in pediatric populations.
- High risk of severe gastrointestinal hemorrhage is a primary clinical concern.
Observation:
- A 4-year-old boy presented with severe hematemesis, melena, and anemia.
- Endoscopy revealed grade III esophageal varices with red signs.
- Imaging demonstrated classic 'spiderweb' appearance of portal cavernoma and associated vascular anomalies.
Findings:
- Laboratory tests indicated severe microcytic hypochromic anemia with normal hepatic and renal function.
- Abdominal ultrasound and CT scan confirmed portal cavernoma and portal hypertensive syndrome.
- An ectopic splenic vein anastomosis was identified.
Implications:
- Portal cavernoma, often overlooked, can be a serious complication of vascular malformations.
- Suspicion of portal cavernoma is vital in pediatric cases of gastrointestinal hemorrhage.
- Timely, tailored management is essential to prevent mortality.
Abstract:
Portal cavernoma is a venous vascular anomaly characterized by the formation of a network of veins whose caliber is increased and carrying portal blood. It is due to a thrombotic and always chronic occlusion of the extra-hepatic portal venous system. This is one of the most common causes of portal hypertension in children. Its severity is mainly associated with an high risk of gastrointestinal haemorrhage. Very few cases have been described mainly in African literature. We report the case of a 4-year old boy admitted with very abundant haematemesis, melena and dizziness associated with anemic syndrome on examination. Laboratory tests showed severe microcytic hypochromic anemia with normal renal and hepatic function. Gastrointestinal endoscopy showed esophageal varices (grade III) with red signs. Abdominal ultrasound showed portal vein formation resulting in the classic "spiderweb", in favor of a cavernoma. Abdominal CT scan confirmed portal cavernoma associated with portal hypertensive syndrome and vascular anomaly like an ectopic splenic vein anastomosis with the trunk formed by the gonadal vein and the inferior mesenteric vein. Therapeutic approach was based on blood transfusion and beta-blocker treatment. Portal cavernoma can be a major complication of vascular malformations often unknown. In case of gastrointestinal haemorrhage in children, diagnosis should be suspected. Its management requires early treatment and should be adapted to the patient's condition in order to prevent a fatal evolution.
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