Case Reports in Neurology (Dec 2018)

Spontaneous Spinal Epidural Haematoma Secondary to Autoimmune Acquired Haemophilia

  • Fardad T. Afshari,
  • Dhruv Parikh,
  • Vladimir Petrik

DOI
https://doi.org/10.1159/000495028
Journal volume & issue
Vol. 10, no. 3
pp. 353 – 356

Abstract

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Spontaneous spinal epidural haematoma is a rare entity associated with high morbidity. Although there are previous reports of spinal haematoma secondary to X-linked genetic haemophilia, there are no such cases secondary to acquired autoimmune haemophilia. We report the case of a 71-year-old patient who presented with sudden quadriplegia secondary to cervical (C2 to T1) epidural haematoma as a result of undiagnosed autoimmune acquired haemophilia A. She underwent emergency cervical laminectomy and evacuation of spinal haematoma with significant recovery in upper limb function. This case highlights the importance of haematological investigations in patients with spontaneous spinal haematoma.

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