Uncommon presentation of choroid plexus papilloma in an infant

Sharad Pandey1, Vivek Sharma1, Kulwant Singh1

  • 1Department of Neuro Surgery, Sir Sunderlal Hospital, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

Insights

A rare choroid plexus papilloma in a child presented unusually with intraventricular hemorrhage and seizures. This case highlights atypical presentations of these primary brain tumors.

Area of Science:

  • Neuro-oncology
  • Pediatric Neurology
  • Neurosurgery

Background:

  • Choroid plexus tumors are rare primary brain neoplasms originating from differentiated epithelial tissue, predominantly well-differentiated papillomas.
  • Commonly found in the fourth ventricle in adults and lateral ventricles in children, these tumors represent a small fraction of central nervous system neoplasms.

Observation:

  • A pediatric case involving a choroid plexus papilloma located in the temporal horn of the lateral ventricle is presented.
  • The patient, a young female, exhibited rare symptoms including sudden intraventricular hemorrhage and recurrent seizures.
  • Notably, the patient did not display typical signs of increased intracranial pressure.

Findings:

  • The case details a choroid plexus papilloma, a type of primary brain tumor, situated within the temporal horn of a lateral ventricle.
  • The tumor's presentation was marked by an acute intraventricular hemorrhage and multiple seizure episodes.
  • Absence of elevated intracranial pressure symptoms was a distinguishing clinical feature.

Implications:

  • This case underscores the importance of considering atypical presentations for choroid plexus tumors, even without classic symptoms.
  • It highlights the diagnostic challenges and varied clinical manifestations of primary brain tumors in pediatric patients.
  • Understanding rare presentations is crucial for timely diagnosis and management of central nervous system neoplasms.

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