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ganglioglioma; dysembryonic neuroepithelial neoplasm

Lumped with dysembryonic neuroepithelial neoplasm - prognosis & treatment the same [2] Epidemiology: - < 30 years of age [2] Pathology: - mixed tumor of neuronal & glial derived cells - may occur anywhere CNS (brain or spinal cord) - majority occur in temporal lobe Genetics: - rare TSC2 gene polymorphism at 3' splice site of intron 4 appears with higher frequency in sporadic gangliogliomas Clinical manifestations: - medication-resistant tumors (90%) Radiology: - magnetic resonance imaging - temporal lobe homogeneous or nodular contrast enhancement [2] Complications: - anticonvulsant-resistant seizures (90%) Management: - neurosurgery: surgical resection - prognosis: - rarely limits life expectancy if completely resected [2]

General

brain neoplasm (intracranial neoplasm) ganglion cell neoplasm glial neoplasm (glioma)

References

  1. Platten et al. J Neuropathol Exp Neurol 56:806-10, 1997
  2. Medical Knowledge Self Assessment Program (MKSAP) 17, 18, 19. American College of Physicians, Philadelphia 2015, 2018, 2021.
  3. WHO classification of Tumors of the Central Nervous System. 4th edition. IARC 2007.

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