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Updated: May 8, 2026

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
Massive per rectal bleeding in a child due to caecal arteriovenous malformation treated successfully by embolisation
Muralidharan Parthasarathy1, Avi Basu, Abdel Rahman Omer
1Department of General Surgery, Ipswich Hospital, Ipswich, UK. dharan76@yahoo.com
Insights
A pediatric patient experienced severe rectal bleeding due to a cecal arteriovenous malformation. Successful treatment was achieved through endovascular embolization, avoiding surgery.
Area of Science:
- Interventional Radiology
- Pediatric Surgery
- Vascular Malformations
Background:
- Arteriovenous malformations (AVMs) are rare vascular anomalies that can present with significant complications.
- Gastrointestinal AVMs, particularly in the pediatric population, pose diagnostic and therapeutic challenges.
- Massive lower gastrointestinal bleeding can lead to hemodynamic instability and shock.
Observation:
- A 12-year-old girl presented with sudden, massive per rectal bleeding and hypotensive shock.
- Computed tomography (CT) angiography revealed active arterial bleeding from a cecal arteriovenous malformation.
- The patient required immediate resuscitation and activation of a massive hemorrhage protocol.
Findings:
- Therapeutic embolization was chosen as the primary treatment modality over immediate surgery.
- The superior mesenteric artery was catheterized via a right femoral approach under local anesthesia.
- Successful embolization of the bleeding vessel was achieved using two microcoils, controlling the hemorrhage.
Implications:
- Endovascular embolization is a viable and effective treatment for pediatric patients with cecal arteriovenous malformations presenting with massive bleeding.
- Minimally invasive endovascular techniques can obviate the need for major surgery in select cases.
- Multidisciplinary collaboration between interventional radiology, surgery, and pediatrics is crucial for optimal management of complex vascular anomalies.
Abstract:
A 12-year-old girl presented with a sudden onset of per rectal bleeding. After admission, she had further episodes of large volume per rectal bleeding and developed hypotensive shock. Hence a massive haemorrhage protocol was activated. Surgical, paediatric and anaesthetic support was sought immediately. Further resuscitation with packed red cells, platelets and fresh frozen plasma was successful. An urgent CT angiogram of the abdomen confirmed active arterial bleeding from an arteriovenous malformation in the caecum. After a detailed discussion between the surgeons and the interventional radiologists, it was decided to attempt therapeutic embolisation first, failing which surgery was the option. The patient and family were fully informed. Through a right femoral approach under local anaesthesia, the superior mesenteric artery was catheterised and the bleeding vessel was successfully controlled with two microembolisation coils. Except for some initial abdominal discomfort, she made an uneventful recovery and was discharged home.
