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Spontaneous epidural spinal haematoma in children caused by vascular malformations
Ramanan Sivakumaran1,2, Andrew King3, Istvan Bodi3
1Department of Neurosurgery, King's College Hospital, London, UK. ramsivakumaran@doctors.org.uk.
Insights
Spinal epidural hematomas are rare in children. This study identifies arteriovenous malformations as a cause in two pediatric cases, offering crucial clinico-pathological insights.
Area of Science:
- Pediatric Neurology
- Vascular Malformations
- Neurosurgery
Background:
- Spinal epidural hematoma (SEH) is uncommon in pediatric populations.
- Spontaneous SEH in children is exceptionally rare, with few documented cases linked to underlying vascular abnormalities.
Observation:
- This study retrospectively reviewed two pediatric cases (<15 years) presenting with spontaneous SEH.
- Both cases revealed underlying arteriovenous malformations (AVMs) as the causative factor.
Findings:
- Intra-operative photographs and histological sections confirmed the presence of AVMs in both pediatric patients.
- This represents the first documented instances of spontaneous pediatric SEH with confirmed underlying AVMs and detailed clinico-pathological correlation.
Implications:
- Highlights the importance of investigating vascular anomalies in pediatric spontaneous SEH.
- Contributes essential clinico-pathological data for understanding rare pediatric neurological conditions.
- Informs diagnostic and surgical approaches for managing spontaneous SEH in children.
Purpose:
The occurrence of spinal epidural haematoma of 'spontaneous' origin in adults is a well-documented entity, though it is rare in children. In the literature to date, there are few cases of this kind of spontaneous haematoma proven to be due to an underlying vascular abnormality.
Method:
Retrospective review of two cases of children under 15 years of age with spontaneous epidural spinal haematoma.
Results:
Underlying arteriovenous malformations were identified in both cases. Intra-operative photographs and histological sections of these anomalies are presented.
Conclusion:
These are the first two such cases described with clinico-pathological correlation.
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