AI Article Synopsis

  • A rare case of hematomyelia caused by a spinal dural arteriovenous fistula (Type I AVM) in a 51-year-old man was presented, highlighting the uncommon occurrence of this condition.
  • The patient experienced severe symptoms including acute epigastric pain, paraplegia, and sensory loss, with imaging revealing a spinal arteriovenous fistula associated with bleeding.
  • Post-surgery, the patient showed limited recovery, regaining only some movement in the left ankle and toe, reinforcing the notion that spinal dural arteriovenous fistulas can lead to hematomyelia, despite its rarity.

Article Abstract

Background Context: Hemorrhage that results from spinal dural arteriovenous fistula (Type I arteriovenous malformation [AVM]) is uncommon. There are some reports of subarachnoid hemorrhage and subdural hematoma caused by Type I spinal AVM, but there are few reported cases of hematomyelia caused by spinal dural arteriovenous fistula.

Purpose: To describe an interesting patient who had hematomyelia caused by a dural arteriovenous fistula (Type I spinal AVM).

Study Design: A case report.

Methods: We present a case of a 51-year-old man who presented acute onset epigastric pain, paraplegia, and sensory loss below his nipples. Magnetic resonance imaging and selective spinal angiogram demonstrated hematomyelia, subarachnoid hemorrhage, and spinal arteriovenous fistula fed by the right Th7 intercostal artery. By laminotomy of Th6-8, the varix-like draining vein and intramedurally hematoma were partially removed and the arterial supply was interrupted by coagulation of the right Th7 segmental artery.

Results: One month after surgery, he regained movement against gravity at the left ankle and toe but no functionally significant improvement.

Conclusions: It must be kept in mind that spinal dural arteriovenous fistulas (Type I spinal AVM) has possibility of hematomyelia origin, despite the fact that it is extremely rare.

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Source
http://dx.doi.org/10.1016/j.spinee.2008.06.449DOI Listing

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