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Cerebral cavernous angiomas in the first year of life

M Gangemi1, P Longatti, F Maiuri

  • 1Institute of Neurosurgery, 2nd School of Medicine, University of Naples, Italy.

Neurosurgery
|September 1, 1989
PubMed

Insights

Cerebral cavernous angiomas are rare in infants, presenting with seizures and head enlargement. Surgical removal is often successful due to the well-defined nature of these brain lesions.

Area of Science:

  • Neurology
  • Pediatric Neurosurgery
  • Neuroradiology

Background:

  • Cerebral cavernous angiomas (CCAs) are uncommon vascular malformations of the brain.
  • CCAs occurring in the first year of life are exceptionally rare, posing diagnostic and management challenges.

Observation:

  • This report details two infant cases of CCA and reviews eleven similar cases from existing literature.
  • Infantile CCAs typically manifest with seizures and progressive head enlargement.
  • Computed tomography (CT) scans reveal large, hyperdense, unenhanced masses with cystic components.

Findings:

  • CCAs in infants must be differentiated from more common pediatric brain tumors like teratomas and ependymomas.
  • Despite their size, CCAs often have minimal bleeding and well-defined margins.
  • Complete surgical resection is frequently achievable for these lesions.

Implications:

  • Early recognition and accurate diagnosis of infantile CCAs are crucial for appropriate management.
  • Surgical intervention offers a viable and often successful treatment option for pediatric CCAs.
  • Further research into the etiology and long-term outcomes of infantile CCAs is warranted.

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