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Acta neurochirurgica · Nov 2004
Review Case ReportsResolution of spinal epidural haematoma without surgery in a haemophilic infant.
- H Iwamuro, A Morita, H Kawaguchi, and T Kirino.
- Department of Neurosurgery, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
- Acta Neurochir (Wien). 2004 Nov 1; 146 (11): 1263-5.
AbstractNon-traumatic spinal epidural haematoma is a rare complication of haemophilia. We report a seven-month-old boy who presented with symptomatic spinal epidural haematoma. He was found to have a hemophilia B trait, and after factor IX replacement, his neurological signs were stabilized and follow-up MRI demonstrated rapid resolution of the haematoma. This illustrative case suggests that surgical intervention can be deferred as the first step in treating spinal epidural haematoma in a haemophilic infant.
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