Pilocytic Astrocytoma: A Review of General, Clinical, and Molecular Characteristics.
Débora SallesGabriela LaviolaAndréa Cristina de Moraes MalinverniJoão Norberto StávalePublished in: Journal of child neurology (2020)
Pilocytic astrocytomas are the primary tumors most frequently found in children and adolescents, accounting for approximately 15.6% of all brain tumors and 5.4% of all gliomas. They are mostly found in infratentorial structures such as the cerebellum and in midline cerebral structures such as the optic nerve, hypothalamus, and brain stem. The present study aimed to list the main characteristics about this tumor, to better understand the diagnosis and treatment of these patients, and was conducted on search of the published studies available in NCBI, PubMed, MEDLINE, Scielo, and Google Scholar. It was possible to define the main histologic findings observed in these cases, such as mitoses, necrosis, and Rosenthal fibers. We described the locations usually most affected by tumor development, and this was associated with the most frequent clinical features. The comparison between the molecular diagnostic methods showed great use of fluorescent in situ hybridization, polymerase chain reaction (PCR), and reverse transcriptase-PCR, important techniques for the detection of BRAF V600E mutation and BRAF-KIAA1549 fusion, characteristic molecular alterations in pilocytic astrocytomas.
Keyphrases
- optic nerve
- end stage renal disease
- high resolution
- real time pcr
- newly diagnosed
- ejection fraction
- prognostic factors
- single molecule
- chronic kidney disease
- subarachnoid hemorrhage
- high grade
- optical coherence tomography
- randomized controlled trial
- multiple sclerosis
- white matter
- quantum dots
- systematic review
- cerebral ischemia
- mass spectrometry
- metastatic colorectal cancer
- functional connectivity
- resting state
- loop mediated isothermal amplification