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Gliosarcoma arising from oligodendroglioma (Oligosarcoma): A case report with genetic analyses.
Tanaka, Shunya; Hitotsumatsu, Tsutomu; Sugita, Yasuo; Ishido, Katsuya; Ito, Osamu; Hatae, Ryusuke; Akagi, Yojiro; Yoshimoto, Koji; Iihara, Koji.
Afiliación
  • Tanaka S; Department of Neurosurgery, Stroke and Neurological Center, Shin-Koga Hospital, Kurume, Japan.
  • Hitotsumatsu T; Department of Neurosurgery, Stroke and Neurological Center, Shin-Koga Hospital, Kurume, Japan.
  • Sugita Y; Department of Pathology, Kurume University School of Medicine, Kurume, Japan.
  • Ishido K; Department of Neurosurgery, Stroke and Neurological Center, Shin-Koga Hospital, Kurume, Japan.
  • Ito O; Department of Neurosurgery, Stroke and Neurological Center, Shin-Koga Hospital, Kurume, Japan.
  • Hatae R; Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Akagi Y; Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Yoshimoto K; Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Iihara K; Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Pathol Int ; 68(10): 567-573, 2018 Oct.
Article en En | MEDLINE | ID: mdl-30246385
ABSTRACT
Gliosarcomas are a type of bimorphic tumor composed of glial and sarcomatous elements, and are considered to be a variant of glioblastoma, WHO grade IV. To date, only rare cases of gliosarcoma with oligodendroglial components (oligosarcoma) have been reported. We report a case of oligosarcoma consisting of gliosarcoma arising from recurrent oligodendroglioma. A 53-year-old man, who had undergone a gross total resection of oligodendroglioma (WHO grade II) 11 years earlier, presented with a local tumor recurrence. The patient underwent a second gross total resection, whereupon a histopathological examination further revealed residual features of classical oligodendroglioma, and newly-developed sarcomatous characteristics. Both the primary and recurrent tumors showed 1p/19q co-deletion and mutation of the isocitrate dehydrogenase 1 (IDH1) gene, consistent with being oligodendroglial in nature. Loss of heterozygosity (LOH) of chromosome 1p/19q and IDH1 mutation have seldom been analyzed in previous reports of oligosarcomas. We report a rare case study supported by the results of genetic analyses. Our analyses have revealed that the sarcomatous component represents a metaplastic change occurring in the oligodendroglial element.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Oligodendroglioma / Neoplasias Encefálicas / Gliosarcoma / Recurrencia Local de Neoplasia / Neoplasias Primarias Múltiples Límite: Humans / Male / Middle aged Idioma: En Revista: Pathol Int Asunto de la revista: PATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Oligodendroglioma / Neoplasias Encefálicas / Gliosarcoma / Recurrencia Local de Neoplasia / Neoplasias Primarias Múltiples Límite: Humans / Male / Middle aged Idioma: En Revista: Pathol Int Asunto de la revista: PATOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Japón