Primary leptomeningeal oligodendroglioma with documented progression to anaplasia and t(1;19)(q10;p10) in a child

Acta Neuropathol. 2009 Oct;118(4):575-7. doi: 10.1007/s00401-009-0565-5. Epub 2009 Jun 27.

Authors

Sabrina Rossi¹, Fausto J Rodriguez, Renan A Mota, Angelo P Dei Tos, Francesco Di Paola, Matteo Bendini, Silvana Agostini, Pierluigi Longatti, Robert B Jenkins, Caterina Giannini

Affiliation

¹ Departments of Pathology, Neuroradiology, Pediatrics and Neurosurgery, Regional Hospital of Treviso, Piazza Ospedale 1, Treviso, Italy. [email protected]

PMID: 19562354
DOI: 10.1007/s00401-009-0565-5

No abstract available

Publication types

Case Reports

MeSH terms

Anaplasia / genetics
Anaplasia / pathology
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 1 / genetics
Chromosomes, Human, Pair 19 / genetics
Disease Progression
Female
Humans
Magnetic Resonance Imaging
Meningeal Neoplasms / genetics
Meningeal Neoplasms / pathology*
Oligodendroglioma / genetics
Oligodendroglioma / pathology*
Spinal Cord / pathology*
Translocation, Genetic