Spontaneous bilateral chronic subdural haematoma in an 8-month-old male with osteogenesis imperfecta: A case report

Authors

  • Ekpene UU Neurosurgery Division, Department of Surgery, University of Uyo Teaching Hospital, Uyo. Akwa Ibom State, Nigeria
  • Uduehe EE Neurosurgery Division, Department of Surgery, University of Uyo Teaching Hospital, Uyo. Akwa Ibom State
  • Isobara I Department of Anaesthesia, University of Uyo Teaching Hospital, Uyo. Akwa Ibom State
  • Ndafia N Neurosurgery Division, Department of Surgery, University of Uyo Teaching Hospital, Uyo. Akwa Ibom State

DOI:

https://doi.org/10.61386/imj.v18i1.611

Keywords:

Osteogenesis imperfecta, Bilateral Chronic Subdural haematoma, genetic collagen disorder, case report

Abstract

Osteogenesis imperfecta is a rare inherited collagen disease that presents most commonly with increased bone fragility. We present an 8-month-old male child with a 5-month history of progressive abnormal increase in the size of the head and a history of multiple long bone fractures not preceded by trauma and blue sclerae. Cranial CT scan showed bilateral frontoparietal chronic subdural haematoma. X-rays of the limbs showed healed left humeral and right femoral fractures.

He underwent bilateral burrhole and drainage of haematoma with a good postoperative outcome.

Osteogenesis imperfecta with spontaneous bilateral chronic subdural haematoma is rare, thus informs this case report.

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Published

01-01-2025