神经外转移性胶质肉瘤1例报告及文献复习

Glioma Pub Date : 2020-04-01 DOI:10.4103/glioma.glioma_7_20
Thara Tunthanathip, Niti Tawaranurak, Kanet Kanjanapradit
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引用次数: 0

摘要

胶质肉瘤(GS)的神经外转移是一种罕见的事件。在本报告中,我们描述了一名15岁的女孩,她患有额叶GS,接受了完全切除,但在3年后出现肿瘤复发,需要进行第二次手术。第二次手术后8个月,她出现左耳后肿块。对临床、神经影像学和组织病理学表现进行了描述。我们还进行了文献综述,确定了26例神经外转移的GS病例,包括目前的报告。伴有颅外转移的GS预后较差,中位生存期约为8.0个月。常见的转移器官是肺(65.4%)、肝(34.6%)和骨骼(23.1%)。我们还讨论了GS与神经外转移的发病机制。我们报告了一例罕见的儿童GS患者神经外转移,生存期长。神经外转移的GS应被视为软组织肿块患者的鉴别诊断。这项工作于2019年9月9日获得泰国宋克拉王子大学医学院伦理委员会的批准(REC 62-259-10-1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extraneural metastatic gliosarcoma: A case report and review of the literature
Extraneural metastasis of gliosarcoma (GS) is a rare event. In this report, we describe a 15-year-old girl with a frontal GS who underwent complete resection, but developed tumor recurrence requiring a second operation after 3 years. Eight months after the second operation, she presented with a left postauricular mass. The clinical, neuroimaging, and histopathological findings were described. We also conducted a literature review and identified 26 cases of GS with extraneural metastasis, including the current report. The prognosis of GS with extracranial metastasis was poor, with a median survival of approximately 8.0 months. The common metastatic organs were the lungs (65.4%), liver (34.6%), and skeleton (23.1%). We also discuss the pathogenesis of GS with extraneural metastasis. We report an unusual case of a pediatric patient with GS with extraneural metastasis, with a long survival. GS with extraneural metastasis should be considered as a differential diagnosis in patients with soft-tissue masses. This work was approved by the Ethics Committee of the Faculty of Medicine, Prince of Songkla University, Thailand (REC 62-259-10-1) on September 9, 2019.
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