Analysis for Stroke Etiology in Duplicated/Accessory MCA-Related Cerebral Infarction: Two Case Report and Brief

Kou Tsuyama1, Nobukazu Miyamoto1, Atsuhiko Shindo1

  • 1Department of Neurology, Juntendo University Hospital, 3-1-3 Hongo, Bunkyo, Tokyo 113-8431, Japan.

Insights

Duplication of the middle cerebral artery (MCA) is rare, but can lead to stroke. This study highlights dissection at the duplicate MCA entry as a key cause of cerebral infarction.

Area of Science:

  • Neurology
  • Vascular Neurology
  • Neuroanatomy

Background:

  • Duplication and accessory forms of the middle cerebral artery (MCA) are uncommon congenital vascular variations.
  • MCA anomalies occur less frequently than other major intracranial artery anomalies.
  • While often found incidentally with subarachnoid hemorrhage due to associated aneurysms, MCA anomalies causing cerebral infarction are rare.

Observation:

  • This report details two cases of cerebral infarction resulting from dissection at the entry point of a duplicated/accessory MCA.
  • Both patients presented with similar clinical courses and dissection sites, notably without headache or preceding injury.
  • Analysis of these cases alongside 20 prior reports revealed a mean age of 55.8 years for MCA infarction, with embolism and dissection as primary etiologies.

Findings:

  • Embolism, often originating from the narrowed proximal segment of the smaller duplicated/accessory MCA, was a significant cause of stroke.
  • Dissection, frequently occurring at the duplication entry site, was another primary mechanism.
  • Potential causes for dissection include medial/endothelial dysfunction or shearing stress at the duplication site.

Implications:

  • The findings suggest that duplicated/accessory MCA should be considered in the differential diagnosis for cerebral infarction, particularly in younger patients or those with unexplained embolic strokes.
  • Understanding the specific mechanisms of dissection in these anomalies is crucial for improved clinical management.
  • Further research into the pathophysiology of dissection in duplicated/accessory MCAs is warranted.

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