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Published on: February 22, 2015
Childhood glioblastoma multiforme of the spinal cord
1Department of Radiation Oncology, Royal Adelaide Hospital, Adelaide, SA, Australia.
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.
Abstract:
Astrocytoma accounts for more than 50% of all central nervous system tumours diagnosed, with particular prevalence in the 15- to 34-year-old age bracket, rarely arising in younger children. In 1995, a 7-year-old boy presented in Emergency with a 3-day history of severe radicular back pain and associated muscle spasms, exacerbated by lying on his back. Both bone scan and plain X-rays were unremarkable; however, MRI showed a 3-cm space-occupying lesion at the level of T5-T6. The patient proceeded to biopsy and partial excision of the tumour through laminectomy, histology confirming an anaplastic astrocytoma (glioblastoma multiforme), St Anne Mayo grade 4. Treatment consisted of a radical course of radiotherapy alone, delivering a total dose of 44.8 Gy at 1.6 Gy per fraction. The treatment comprised of three phases using two oblique wedged fields on a 6 MV linear accelerator. The patient remains disease free 7 years post treatment, with the only effect noted being a slight kyphoscoliosis at the site of the laminectomy and radiation. This report highlights the efficacy of combined surgery and radiation therapy in the management of spinal cord glioblastoma multiforme in preventing tumour recurrence, with acceptable morbidity. Further evaluation of the treatment efficacy would be difficult because of the scarcity of such cases.
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