Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma
2007

Trisomy 19 Ependymoma: A New Type of Brain Tumor

Sample size: 149 publication Evidence: moderate

Author Information

Author(s): Rousseau Emmanuel, Palm Thomas, Scaravilli Francesco, Ruchoux Marie-Magdeleine, Figarella-Branger Dominique, Salmon Isabelle, Ellison David, Lacroix Catherine, Chapon Françoise, Mikol Jacqueline, Vikkula Miikka, Godfraind Catherine

Primary Institution: Université catholique de Louvain, Bruxelles, Belgium

Hypothesis

Is there a distinct genetic and histological association in ependymomas characterized by trisomy 19?

Conclusion

Trisomy 19 ependymomas are a newly identified subgroup of ependymal tumors with specific genetic and histological features.

Supporting Evidence

  • Trisomy 19 was present in all analyzed tumors with the specific histological features.
  • Deletions on chromosome 9 were observed in 78% of the tumors with trisomy 19.
  • Histologically, trisomy 19 ependymomas are characterized by a branched capillary network and regularly dispersed tumoral cells.

Takeaway

Some brain tumors called ependymomas can have a special change in their genes, known as trisomy 19, which helps doctors understand them better.

Methodology

The study analyzed 149 formalin-fixed and paraffin-embedded ependymomas using microsatellite analysis and array comparative genomic hybridization (array-CGH).

Potential Biases

There may be risks of bias due to the reliance on archived tumor samples from multiple centers.

Limitations

The study is limited by the retrospective nature of the tumor sample collection and the potential for selection bias.

Participant Demographics

The age at diagnosis ranged from 0.4 to 30 years, with a mean age of 14 years.

Statistical Information

P-Value

< 0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1186/1476-4598-6-47

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication