Brain Stem Gliomas pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]

Overview

Brainstem gliomas may arise from glial cells of the brainstem, a majority of these tumors are found in the pons. Other areas include tectal area and medulla. Genetic mutations in histone genes, activin A receptor gene, tyrosine kinase mutations and TP53 mutations have been implicated in the development of brain stem gliomas. On gross pathology, brainstem gliomas can be classified into four subtypes: diffuse, focal, dorsal exophytic and cervicomedullary. Each of the four subtypes has its distinct microscopic pathology.

Pathophysiology

Cytogenetic Characteristics of Diffuse Intrinsic Pontine Gliomas (DIPGs)

Diffuse brainstem gliomas also known as diffuse intrinsic pontine gliomas (DIPGs) as the name suggests are predominantly present in the pons. DIPGs exhibit genotypic modifications that differ from other high grade gliomas, both adult and pediatric. The gene expression profile of DIPG also varies from that of non–brain stem pediatric high-grade gliomas, further supporting a distinctive biology for this subset of pediatric gliomas. DIPG patirents may have the following genomic abnormalities:[1]

  • Histone H3 genes: Approximately 80% of DIPG tumors have a mutation in a specific amino acid in the histone H3.1 (H3F3A) or H3.3 (HIST1H3B) genes. These same mutations are observed in pediatric high-grade gliomas at other midline locations but are uncommon in cortical pediatric high-grade gliomas and in adult high-grade gliomas.[2]
  • Activin A receptor, type I (ACVR1) gene: Approximately 20% of DIPG cases have activating mutations in the ACVR1 gene, with most occurring concurrently with H3.3 mutations. Germline mutations in ACVR1 cause the autosomal dominant syndrome fibrodysplasia ossificans progressiva (FOP), although there is no cancer predisposition in FOP.
  • Receptor tyrosine kinase amplification: PDGFRA amplification occurs in approximately 30% of cases, with lower rates of amplification observed for some other receptor tyrosine kinases (e.g., MET and IGF1R).
  • TP53 deletion: DIPG tumors commonly show deletion of the TP53 gene on chromosome 17p. Additionally, TP53 is commonly mutated in DIPG tumors, particularly those with histone H3 gene mutations. Aneuploidy is commonly observed in cases with TP53 mutations.

Gross pathology

Brain stem gliomas may occur in the pons, midbrain, tectum, dorsum of the medulla at the cervicomedullary junction, or in multiple regions of the brain stem. As a general rule, mesencephalic tumors tend to be of a lower grade than those in the pons and medulla.

  • Most common location
  • Classic location for the childhood 'brainstem glioma' which tends to refer to a diffuse pontine glioma
  • Focal dorsally exophytic brainstem glioma is an uncommon variant accounting for only 10% of pontine tumours, and has a much better prognosis, as it usually represents a pilocytic astrocytoma
  • Overall survival of pontine gliomas is 10% at 5 years
  • Mesencephalic[4]
    • Includes diffuse, focal, exophytic and tectal variants.
    • Focal brainstem gliomas are more common here than elsewhere in the brainstem
    • Tectal plate gliomas are typically indolent
  • Medullary
    • Least common location
    • Includes focal dorsally exophytic, focal, diffuse and cervicomedullary junction variants
    • Cervicomedullary junction tumours usually represent upper cervical tumours extending superiorly
    • Most common location for NF1-associated tumors

Microscopic pathology

The brain stem gliomas are classified into 4 subtypes, and each has its distinct histological features:[5]

References

  1. Pathophysiology of brainstem gliomas. NIH National cancer institute. http://www.cancer.gov/types/brain/hp/child-glioma-treatment-pdq#section/_35
  2. Uekawa K, Nakamura H, Shinojima N, Takezaki T, Yano S, Kuratsu JI (April 2016). "Adult Diffuse Astrocytoma in the Medulla Oblongata: Molecular Biological Analyses Including H3F3A Mutation of Histone H3.3". NMC Case Rep J. 3 (2): 29–33. doi:10.2176/nmccrj.cr.2015-0012. PMC 5386147. PMID 28663993.
  3. Warren KE (2012). "Diffuse intrinsic pontine glioma: poised for progress". Front Oncol. 2: 205. doi:10.3389/fonc.2012.00205. PMC 3531714. PMID 23293772.
  4. Boydston WR, Sanford RA, Muhlbauer MS, Kun LE, Kirk E, Dohan FC, Schweitzer JB (1991). "Gliomas of the tectum and periaqueductal region of the mesencephalon". Pediatr Neurosurg. 17 (5): 234–8. doi:10.1159/000120603. PMID 1822688.
  5. Pathophysiology of Brainstem gliomas. Dr Yuranga Weerakkody and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/brainstem-glioma
  6. Uekawa K, Nakamura H, Shinojima N, Takezaki T, Yano S, Kuratsu JI (April 2016). "Adult Diffuse Astrocytoma in the Medulla Oblongata: Molecular Biological Analyses Including H3F3A Mutation of Histone H3.3". NMC Case Rep J. 3 (2): 29–33. doi:10.2176/nmccrj.cr.2015-0012. PMC 5386147. PMID 28663993.

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