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[Clinicopathoradiological studies in 15 cases of megadolichobasilar anomaly]

Y Okada1, T Shima, M Nishida

  • 1Department of Neurosurgery, Chugoku Rousai Hospital, Kure, Japan.

No to Shinkei = Brain and Nerve
|March 1, 1994
PubMed

Insights

Megadolichobasilar anomalies, characterized by elongated and widened basilar arteries, are associated with severe neurological symptoms and poor outcomes. This study highlights the critical need for early diagnosis and management of these rare vascular conditions.

Area of Science:

  • Neurology
  • Vascular Neurology
  • Neuroradiology

Background:

  • Megadolichobasilar anomaly (MDBA) is a rare condition involving abnormal elongation and widening of the basilar artery.
  • Clinical presentation often includes ischemic events, headaches, or trigeminal neuralgia.
  • Severe hypertension is a common comorbidity.

Observation:

  • This study assessed 15 patients with angiographically diagnosed MDBA.
  • Patients averaged 61 years old, with a slight male predominance (9 males, 6 females).
  • Common symptoms included cerebral ischemic attacks (11 patients), trigeminal neuralgia (2 patients), and severe headaches (2 patients).

Findings:

  • Vertebral angiography revealed marked basilar artery elongation, tortuosity, and dilatation (average diameter 8.6 mm).
  • CT scans showed a characteristic tubular, contrast-enhancing high-density mass.
  • Four patients exhibited aneurysmal dilatation of the basilar artery.

Implications:

  • MDBA is associated with a high rate of severe morbidity and mortality.
  • Poor outcomes included 5 deaths and 4 cases of severe dementia among the 15 patients.
  • Findings underscore the importance of recognizing MDBA for appropriate clinical management and prognosis.

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