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Glioblastoma Multiforme Involving Conus Medullaris in a Child
Muhammad Atif Mansha1, Agha Muhammad Hammad Khan1, Ahmed Nadeem N Abbasi1
1Oncology, Aga Khan University, Karachi, PAK.
Insights
Spinal cord glioblastoma multiforme (GBM) in the conus medullaris is rare and has a poor prognosis. This case study details a child
Area of Science:
- Neuro-oncology
- Pediatric neurosurgery
- Spinal cord tumors
Background:
- Primary spinal cord glioblastoma multiforme (GBM) involving the conus medullaris is exceptionally rare.
- Limited established treatment guidelines exist for spinal GBM, contributing to poor patient outcomes.
Observation:
- A pediatric case of conal GBM was treated with surgery and adjuvant chemoradiation.
- The patient experienced initial symptomatic improvement followed by clinical deterioration.
Findings:
- Aggressive multimodality treatment, including surgery and chemoradiation, did not alter the poor prognosis for this pediatric conal GBM.
- The stepwise treatment approach highlights the challenges in managing this rare spinal cord tumor.
Implications:
- This case underscores the need for further research into effective treatments for spinal GBM.
- Developing specific treatment guidelines for pediatric spinal GBM is crucial for improving patient outcomes.
Abstract:
Primary spinal cord glioblastoma multiforme involving the conus medullaris is an uncommon entity with poor outcomes. An aggressive multimodality treatment approach has been used, but prognosis remains same. There are no guidelines for the treatment of patients with spinal glioblastoma multiforme (GBM). We highlight the case of a child diagnosed with conal GBM. He was treated with definitive surgery followed by adjuvant concurrent chemoradiation. After completion of treatment, he showed a temporary symptomatic improvement, but later on his condition deteriorated. We elaborate the stepwise treatment approach employed in this patient.
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