Spontaneous Spinal Epidural Hematoma: A Case Report and Literature Review

Abstract Background: Spontaneous spinal epidural hematoma (SSEH) is a rare cause of spinal cord compression that requires emergency investigation and treatment. Prompt diagnosis is essential to prevent morbidity and mortality. Objectives: Our goal was to report a case of SSEH, and to review the lite...

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Bibliographic Details
Published in:The Journal of emergency medicine 2012-02, Vol.42 (2), p.e31-e34
Main Authors: Hussenbocus, Saleem M., MBBS, Wilby, Martin J., PHD, Cain, Chris, FRACS, Hall, David, FRACS
Format: Article
Language:English
Subjects:
Adult
Emergency
epidural
hematoma
Hematoma, Epidural, Spinal - complications
Hematoma, Epidural, Spinal - diagnosis
Humans
Magnetic Resonance Imaging
Male
Paraplegia - etiology
review
spinal
Spinal Cord Compression - etiology
spontaneous
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Summary:Abstract Background: Spontaneous spinal epidural hematoma (SSEH) is a rare cause of spinal cord compression that requires emergency investigation and treatment. Prompt diagnosis is essential to prevent morbidity and mortality. Objectives: Our goal was to report a case of SSEH, and to review the literature on the topic, looking particularly at the factors influencing post-operative outcome, and the symptoms and signs that would lead one to consider this rare diagnosis. Case Report: A 36-year-old man presented to the Emergency Department with paraplegia and a sensory level at T4. There was no history of trauma and he was not taking any medications. Magnetic resonance imaging revealed a large non-enhancing posterior epidural mass lesion between C7 and upper T4, causing severe cord compression at T1–T3. Post contrast scans revealed no rim enhancement. Blood investigations were unremarkable, with an international normalized ratio of 1.1. He underwent urgent decompression laminectomy within 12 h of symptom onset. Intraoperatively, thick clotted blood and prominent epidural vessels were seen. Histology revealed engorged vessels with hemorrhage and clot in the extravascular tissues. Post-operatively, the impaired neurological status remained unchanged. Conclusion: SSEH is a rare cause of spinal cord compression that requires prompt diagnosis and surgical intervention to prevent morbidity. Neurological outcome after surgical decompression depends on the severity of preoperative neurological deficits as well as the time between symptom onset and surgery.
ISSN:0736-4679
2352-5029
DOI:10.1016/j.jemermed.2008.08.008