Childhood glioblastoma multiforme of the spinal cord

C Oake1, M F Borg, A Hanieh

  • 1Department of Radiation Oncology, Royal Adelaide Hospital, Adelaide, SA, Australia.

Australasian Radiology
|August 4, 2006
PubMed

Insights

This case study shows that surgery combined with radiation therapy can effectively manage spinal cord glioblastoma multiforme, preventing recurrence with minimal side effects. The 7-year-old patient remained disease-free for 7 years post-treatment.

Area of Science:

  • Neuro-oncology
  • Radiation Oncology
  • Pediatric Neurosurgery

Background:

  • Astrocytoma, a common central nervous system tumor, rarely affects children.
  • Spinal cord glioblastoma multiforme is an aggressive tumor with a poor prognosis.

Observation:

  • A 7-year-old boy presented with severe back pain due to a T5-T6 space-occupying lesion.
  • MRI revealed a 3-cm lesion consistent with anaplastic astrocytoma (glioblastoma multiforme, WHO grade 4).

Findings:

  • The patient underwent laminectomy, partial tumor excision, and radiotherapy (44.8 Gy).
  • Histology confirmed anaplastic astrocytoma (glioblastoma multiforme), WHO grade 4.
  • The patient remained disease-free for 7 years post-treatment, with minor kyphoscoliosis.

Implications:

  • Combined surgical resection and radiotherapy demonstrate efficacy in managing spinal glioblastoma.
  • This approach offers a favorable outcome with acceptable morbidity in pediatric cases.
  • The rarity of spinal glioblastoma multiforme necessitates further case studies for comprehensive understanding.