AI Article Synopsis

  • Astroblastoma is a rare brain tumor mainly affecting older children, typically found in the frontoparietal regions of the brain.
  • A 32-year-old woman experienced a recurrence of her astroblastoma 21 years after it was initially removed and treated with radiation, now presenting with seizures and imaging showing significant tumor growth.
  • The surgical removal utilized a technique called 5-aminolevulinic acid (5-ALA), which helped in the resection process, and genetic testing of the tumor identified specific fusion transcripts linked to its development.

Article Abstract

Background: Astroblastoma is a rare neoplasm characterized as a circumscribed glial neoplasm most often arising in the frontoparietal cerebral hemispheres in older children.

Observations: We report an intriguing case of an astroblastoma recurrence 21 years after gross-total resection and radiation. A 32-year-old right-handed female presented to the emergency department for a generalized tonic-clonic seizure. She had a history of bipolar disorder, intractable migraines, and prior seizures linked to an astroblastoma previously resected three times. Magnetic resonance imaging on the current visit showed growth of the recurrent lesion to a 3.8-cm maximal diameter. Left-sided awake craniotomy was performed to remove the tumor while using speech mapping and 5-aminolevulinic acid (5-ALA). Targeted next-generation sequencing of the tumor revealed in-frame MN1::BEND2 fusion transcripts.

Lessons: We found that 5-ALA can be used in astroblastoma patients to assist in gross-total resection, which is important for long-term survival. Our astroblastoma case demonstrated classic astroblastoma morphology, with typical perivascular astroblastic rosettes, and was brightly fluorescent after 5-ALA administration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618070PMC
http://dx.doi.org/10.3171/CASE23526DOI Listing

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