Infant with unusually large choroid plexus papilloma undergoing emergency surgery. Case report with special emphasis

T Picht1, J Jansons, A van Baalen

  • 1Department of Neurosurgery, Charité, Universitatsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany. thomas.picht@charite.de

Pediatric Neurosurgery
|February 9, 2006
PubMed

Insights

Choroid plexus papillomas are common infant brain tumors. A large tumor in a 3-month-old was successfully removed, leading to a full recovery despite critical symptoms.

Area of Science:

  • Pediatric Neurosurgery
  • Neuropathology
  • Neuro-oncology

Background:

  • Choroid plexus papillomas are frequent central nervous system tumors in infants.
  • Symptoms like hydrocephalus and vomiting can delay diagnosis until critical stages.

Observation:

  • A 3-month-old infant presented with a large (7x8x6 cm) choroid plexus papilloma in the right lateral ventricle.
  • The infant exhibited acute herniation symptoms with fixed, dilated pupils, indicating a critical clinical state.

Findings:

  • Despite the tumor's significant size, proximity to eloquent brain areas, and the infant's critical condition, complete surgical resection was achieved.
  • The infant experienced a complete clinical recovery post-surgery.

Implications:

  • This case highlights the possibility of successful surgical intervention and complete recovery even in neonates with large, critically located brain tumors.
  • Early diagnosis and prompt surgical management are crucial for improving outcomes in infant choroid plexus papilloma cases.

Related Concept Videos