Resolution of spinal epidural haematoma without surgery in a haemophilic infant.

Iwamuro, H; Morita, A; Kawaguchi, H; Kirino, T · Acta Neurochir (Wien) · 2004

case_report · Level V

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Abstract

Non-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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