Sarcomatous transformation of IDH-mutant astrocytoma matching to methylation class oligosarcoma following embolization, a case report

The mesenchymal transformations of infiltrating gliomas are uncommon events. This is particularly true of IDH-mutant astrocytomas and oligodendrogliomas, in which mesenchymal transformation is exceedingly rare. oligosarcoma is a newly recognized methylation class (MC) that represents transformed 1p/19q co-deleted oligodendrogliomas, but recent studies indicate it may be non-specific. Herein we report the diffuse sarcomatous transformation of a multifocal recurrent astrocytoma from a precursor IDH-mutant astrocytoma, CNS WHO grade 3, in a young patient following embolization therapy and matching to MC oligosarcoma. The sarcomatous recurrence and original tumor showed identical 17q breakpoints with loss of heterozygosity of TP53. Both lack the defining 1p/19q co-deletion or copy-neutral heterozygosity of an oligodendroglioma and oligosarcoma. The findings in this case report both contribute to the apparent heterogeneity of the novel MC oligosarcoma and describe a second reported mesenchymal transformation of an IDH-mutant astrocytoma.

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Journal
Acta Neuropathologica Communications
Published
2024-12-20
DOI
https://doi.org/10.1186/s40478-024-01908-7
Citations
3
Primary Topic
Glioma Diagnosis and Treatment
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article
Field-Weighted Citation Impact
1.31
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article

Sarcomatous transformation of IDH-mutant astrocytoma matching to methylation class oligosarcoma following embolization, a case report

Sean P. Ferris, Wajd N. Al‐Holou, Kyle Conway, Lina Shao et al.
3 citations
Acta Neuropathologica Communications
Glioma Diagnosis and Treatment
1.31
article

Sarcomatous transformation of IDH-mutant astrocytoma matching to methylation class oligosarcoma following embolization, a case report

Sean P. Ferris, Wajd N. Al‐Holou, Kyle Conway, Lina Shao, Arushi Tripathy, Edwin Nieblas‐Bedolla, Ryan Landvater
article en
3 citations

Abstract

The mesenchymal transformations of infiltrating gliomas are uncommon events. This is particularly true of IDH-mutant astrocytomas and oligodendrogliomas, in which mesenchymal transformation is exceedingly rare. oligosarcoma is a newly recognized methylation class (MC) that represents transformed 1p/19q co-deleted oligodendrogliomas, but recent studies indicate it may be non-specific. Herein we report the diffuse sarcomatous transformation of a multifocal recurrent astrocytoma from a precursor IDH-mutant astrocytoma, CNS WHO grade 3, in a young patient following embolization therapy and matching to MC oligosarcoma. The sarcomatous recurrence and original tumor showed identical 17q breakpoints with loss of heterozygosity of TP53. Both lack the defining 1p/19q co-deletion or copy-neutral heterozygosity of an oligodendroglioma and oligosarcoma. The findings in this case report both contribute to the apparent heterogeneity of the novel MC oligosarcoma and describe a second reported mesenchymal transformation of an IDH-mutant astrocytoma.

Acta Neuropathologica CommunicationsVol. 12(1)
University of Michigan (US)
Good health and well-being
Openalex Percentile: Top 17%
Glioma Diagnosis and Treatment
1.31
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Sarcomatous transformation of IDH-mutant astrocytoma matching to methylation class oligosarcoma following embolization, a case report — Sean P. Ferris, Wajd N. Al‐Holou, et al. · Acta Neuropathologica Communications (2024) | TGRS Research Map | TGRS