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Sarcoma-like tumor originating from oligodendroglioma.

Abstract
We present a case of sarcoma occurring at a site of resected oligodendroglioma without preceding radiotherapy or chemotherapy. Oligosarcoma occurring at sites of resected oligodendroglioma or anaplastic oligodendroglioma with sarcomatous components are rare. Although meningioma or sarcoma-like lesions are sometimes reported after glioma-targeted radiotherapy, those without preceding radiotherapy are quite rare. Moreover, cases of sarcoma without oligodendroglial components occurring at a site of resected oligodendroglioma have never been reported. In this case, fluorescent in situ hybridization analysis revealed 1p/19q co-deletion in both the first tumor and second tumors. Additionally, immunohistochemistry revealed mutated isocitrate dehydrogenase 1 in both tumors. Taken together, these findings suggest a monoclonal tumor origin. Consequently, this case may indicate a new mechanism of development of sarcomatous lesions occurring at the site of a resected glioma.
AuthorsTakuhiro Shoji, Ryuta Saito, Masayuki Kanamori, Yukihiko Sonoda, Mika Watanabe, Teiji Tominaga
JournalBrain tumor pathology (Brain Tumor Pathol) Vol. 33 Issue 4 Pg. 255-260 (Oct 2016) ISSN: 1861-387X [Electronic] Japan
PMID27333891 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Isocitrate Dehydrogenase
Topics
  • Adult
  • Brain Neoplasms (diagnosis, genetics, pathology, surgery)
  • Cell Transformation, Neoplastic
  • Chromosomes, Human, Pair 1 (genetics)
  • Chromosomes, Human, Pair 19 (genetics)
  • Gene Deletion
  • Humans
  • Isocitrate Dehydrogenase (genetics)
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Neoplasms, Multiple Primary
  • Oligodendroglioma (diagnosis, genetics, pathology, surgery)
  • Sarcoma (diagnosis, genetics, pathology, surgery)

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