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Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
[Primary intraventricular hemorrhage as a result of a bleeding arteriovenous malformation]
M E Vázquez-López1, R Pego-Reigosa
1Servicio de Pediatría, Complejo Hospitalario Xeral-Calde, 27004 Lugo, España. esther.vazquez.lopez@sergas.es
Insights
Primary intraventricular hemorrhage is rare in children. A 15-year-old girl’s arteriovenous malformation was successfully treated with radiosurgery, highlighting the need to identify underlying causes.
Area of Science:
- Neurology
- Neurosurgery
- Radiology
Background:
- Primary intraventricular hemorrhage (IVH) is exceptionally rare in pediatric patients.
- Prompt diagnosis and identification of underlying vascular lesions are crucial for effective management.
Observation:
- A 15-year-old female presented with sudden severe headache, vomiting, and fever, exhibiting only neck stiffness on examination.
- Brain computed tomography revealed intraventricular hemorrhage.
- Conventional angiography identified an arteriovenous malformation (AVM) in the right pericallosal artery branches.
Findings:
- Gamma-knife radiosurgery was performed for the AVM with no immediate complications.
- Follow-up angiography confirmed the complete disappearance of the arteriovenous malformation.
- This case underscores the importance of investigating potential underlying lesions in pediatric IVH.
Implications:
- Early detection and treatment of AVMs are vital in pediatric intraventricular hemorrhage cases.
- Treatment modalities for AVMs include surgery, interventional radiology, and radiosurgery, often used in combination.
- This case highlights radiosurgery as an effective treatment option for pediatric intraventricular AVMs.
Abstract:
Primary intraventricular hemorrhage is very rare in adults and is even more infrequent in children. We present a 15-year-old girl who presented to the hospital because of sudden severe headache, vomiting and fever. Neurological examination only showed neck stiffness. A brain computed tomography showed blood in the ventricular system. Conventional angiography revealed an arteriovenous malformation originating in the right pericallosal artery branches. Gamma-knife radiosurgery was performed without relevant complications. A follow-up cerebral angiography showed disappearance of the arteriovenous malformation. When a primary intraventricular hemorrhage is detected in a young patient it is mandatory to rule out an underlying lesion such an arteriovenous malformation. Treatment options include surgery, interventional radiology and radiosurgery, alone or in combination.
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