Jugular foramen schwannoma in a child treated with complete surgical excision

Meharpal Sangra1, Conor Mallucci, Barry Pizer

  • 1Department of Neurosurgery, Royal Liverpool Children's Hospital, Liverpool, UK. rsangra@doctors.org.uk

Insights

A rare jugular foramen schwannoma was found in a pediatric patient presenting as a posterior fossa mass. This case highlights the importance of considering schwannoma in the differential diagnosis of pediatric jugular foramen tumors.

Area of Science:

  • Neurosurgery
  • Pediatric Oncology
  • Pathology

Background:

  • Jugular foramen tumors are rare, especially in pediatric patients.
  • Posterior fossa masses can originate from the jugular foramen.
  • Schwannomas are typically benign nerve sheath tumors.

Observation:

  • A 13-year-old boy presented with symptoms of increased intracranial pressure.
  • MRI revealed a large tumor originating from the jugular foramen, suggestive of schwannoma.
  • The tumor presented as a posterior fossa mass.

Findings:

  • Complete surgical excision of the jugular foramen schwannoma was achieved in a single stage via lateral suboccipital craniotomy.
  • The patient experienced minimal morbidity following the procedure.
  • Histopathology confirmed the tumor as a WHO Grade I schwannoma.

Implications:

  • This case underscores the rarity of jugular foramen schwannoma in children.
  • Accurate imaging is crucial for diagnosing jugular foramen tumors.
  • Differential diagnoses for jugular foramen tumors include glomus jugulare, meningiomas, schwannomas, myxomas, and chondrosarcomas.
Abstract