Abstract
Background
Bilateral thalamic astrocytomas in children are exceedingly rare. These highly malignant tumors seldom respond to conventional treatment strategies and carry a grim prognosis for patients. However, recent advances in molecular oncology have had a positive impact on prognostication and treatment strategies of these tumors.
Case-based review
We present a new case of WHO grade III bilateral thalamic astrocytoma in a child and review the pathophysiology, molecular oncogenesis, and relevant treatment strategies for this rare disease.
Conclusions
High-grade thalamic astrocytomas affecting both thalami pose a challenge to pediatric neurosurgeons, neuro-oncologists, and neuropathologists given the lack of effective treatment strategies. Understanding recent revelations in the field of molecular oncology can assist clinicians in adequately formulating a treatment plan in this patient population.
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Goodarzi, A., Garza, N., Lechpammer, M. et al. The molecular oncology of bilateral high-grade thalamic astrocytomas in children. Childs Nerv Syst 35, 2047–2054 (2019). https://doi.org/10.1007/s00381-019-04372-0
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DOI: https://doi.org/10.1007/s00381-019-04372-0