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起源于少突胶质细胞瘤的胶质肉瘤(少突胶质肉瘤):一例基因分析病例报告

Gliosarcoma arising from oligodendroglioma (Oligosarcoma): A case report with genetic analyses.

作者信息

Tanaka Shunya, Hitotsumatsu Tsutomu, Sugita Yasuo, Ishido Katsuya, Ito Osamu, Hatae Ryusuke, Akagi Yojiro, Yoshimoto Koji, Iihara Koji

机构信息

Department of Neurosurgery, Stroke and Neurological Center, Shin-Koga Hospital, Kurume, Japan.

Department of Pathology, Kurume University School of Medicine, Kurume, Japan.

出版信息

Pathol Int. 2018 Oct;68(10):567-573. doi: 10.1111/pin.12723. Epub 2018 Sep 23.

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.

摘要

胶质肉瘤是一种由神经胶质和肉瘤成分组成的双相性肿瘤,被认为是胶质母细胞瘤(世界卫生组织IV级)的一种变体。迄今为止,仅有罕见的伴有少突胶质细胞成分的胶质肉瘤(少突肉瘤)病例报道。我们报告一例由复发性少突胶质细胞瘤发展而来的少突肉瘤病例。一名53岁男性,11年前曾接受少突胶质细胞瘤(世界卫生组织II级)的全切除手术,现出现局部肿瘤复发。患者接受了第二次全切除手术,组织病理学检查进一步显示有经典少突胶质细胞瘤的残留特征以及新出现的肉瘤特征。原发肿瘤和复发肿瘤均显示1p/19q共缺失和异柠檬酸脱氢酶1(IDH1)基因突变,符合少突胶质细胞性质。以往少突肉瘤的报道中很少分析1p/19q染色体杂合性缺失(LOH)和IDH1突变情况。我们报告一项有基因分析结果支持的罕见病例研究。我们的分析表明,肉瘤成分代表少突胶质细胞成分发生的化生改变。

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