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Updated: Aug 29, 2026

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
[Severe complications in the treatment of vascular anomalies]
L F Avila1, J C López Gutiérrez, M Díaz
1Departamento de Cirugía Pediátrica, Hospital Infantil La Paz, Paseo de la Castellana 261, 28046 Madrid.
Insights
Accurate diagnosis and appropriate treatment sequencing are crucial for managing infantile vascular anomalies. Improper management can lead to severe complications, highlighting the need for careful therapeutic strategies.
Area of Science:
- Pediatric vascular anomalies
- Treatment complications
- Infant health
Background:
- Vascular anomalies in infants require precise diagnosis and management.
- Treatment options include pharmacologic, endovascular, surgical, and laser therapies.
- Therapeutic outcomes vary, and potential complications must be considered.
Observation:
- Review of patients with vascular anomalies experiencing major treatment-related complications over five years.
- Documented cases include hemangiomas, Blue-Rubber Bleb Nevus syndrome, arteriovenous malformations, and Kaposi-like hemangio-endothelioma.
- Complications ranged from neutropenia and neurological deficits to skin necrosis, limb ischemia, and fatal infections.
Findings:
- Interferon treatment for steroid-resistant hemangiomas led to neutropenia and neurological issues.
- Percutaneous sclerosis for Blue-Rubber Bleb Nevus syndrome resulted in skin necrosis and nerve paralysis.
- Surgical intervention for arteriovenous malformations caused ischemia and necessitated amputation.
- Prolonged steroid therapy for hemangio-endothelioma resulted in fatal meningoencephalitis.
Implications:
- Early and accurate diagnosis is paramount for effective vascular anomaly treatment in children.
- Incorrect therapeutic sequences can render treatments ineffective or hazardous.
- Careful treatment planning can prevent many severe complications in pediatric patients.
Background:
Success in the treatment of vascular anomalies during infancy depends on an accurate early diagnosis and a correct therapeutic management. Current available resources can be divided into pharmacologic, endovascular, surgical, and laser. Results are variable, and complications should always be kept in mind.
Methods:
We reviewed all patients with vascular anomalies who suffered from major complications directly due to the treatment during the past five years.
Results:
1. A patient with an upper lip hemangioma following treatment with interferon after no response to steroids. A long-term severe neutropoenia forced to an early surgical excision of the lesion. 2. A patient suffering from an orbitary hemangioma with severe exoftalmus was treated with interferon because of a steroid-resistance. A spastic diplegia due to interferon reverted after treatment was discontinued. 3. In a patient with a Blue-Rubber Bleb Nevus syndrome, extended percutaneous sclerosis was performed. She developed skin necrosis of the left leg and a permanent sciatic nerve paralysis. 4. In a patient with an arteriovenous malformation on the right leg and gluteous, a femoral artery endoprosthesis was placed because of a massive bleeding. She underwent a total excision of the malformation and developed a recurrent ischemia related to a femoral thrombosis. Finally a foot amputation was needed. 5. A patient with a Kaposi-like hemangio-endothelioma who was following a high-dose prolonged steroid therapy died because of a meningoencephalitis related to a severe immunosuppression.
Conclusions:
Treatment of vascular anomalies during childhood need an early accurate diagnosis. If a right therapeutic sequence is not performed, useful drugs can turn into inefficient or dangerous. Most treatment complications in these patients can be avoided.
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