Synchronous gemistocytic astrocytoma IDH-mutant and oligodendroglioma IDH-mutant and 1p/19q-codeleted in a patient with CCDC26 polymorphism

Acta Neuropathol. 2017 Aug;134(2):317-319. doi: 10.1007/s00401-017-1727-5. Epub 2017 May 26.

Authors

Rachael A Vaubel¹, Thomas M Kollmeyer², Alissa A Caron², Emily G Barr Fritcher³, Jesse S Voss³, Haohai Liang⁴, Robert B Jenkins², Caterina Giannini¹, Benjamin R Kipp⁵

Affiliations

¹ Department of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
² Department of Experimental Pathology, Mayo Clinic, Rochester, MN, USA.
³ Department of Molecular Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
⁴ Anatomic Pathology, WellStar Kennestone Hospital, Marietta, GA, USA.
⁵ Department of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA. [email protected].

PMID: 28550371
DOI: 10.1007/s00401-017-1727-5

No abstract available

Publication types

Case Reports
Research Support, N.I.H., Extramural

MeSH terms

Brain Neoplasms / diagnostic imaging
Brain Neoplasms / genetics*
Chromosome Deletion*
Chromosomes, Human, Pair 1 / genetics*
Chromosomes, Human, Pair 19 / genetics*
Glioma / diagnostic imaging
Humans
Intracellular Signaling Peptides and Proteins / genetics
Isocitrate Dehydrogenase / genetics*
Magnetic Resonance Imaging
Male
Middle Aged
Mutation / genetics*
RNA, Long Noncoding
X-linked Nuclear Protein / metabolism

Substances

Intracellular Signaling Peptides and Proteins
RNA, Long Noncoding
long noncoding RNA CCDC26, human
Isocitrate Dehydrogenase
IDH1 protein, human
ATRX protein, human
X-linked Nuclear Protein