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放射治疗诱发的两个异时性肿瘤:病例报告及文献复习

Two metachronous tumors induced by radiation therapy: case report and review of the literature.

作者信息

Sasayama Takashi, Nishihara Masamitsu, Tanaka Kazuhiro, Mizukawa Katsu, Ehara Kazumasa, Kanomata Naoki, Kohmura Eiji

机构信息

Department of Neurosurgery, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Japan.

出版信息

J Neurooncol. 2008 Jul;88(3):315-20. doi: 10.1007/s11060-008-9570-0. Epub 2008 Mar 29.

Abstract

Various radiation-induced tumors, including meningioma, glioma, and sarcoma, have been reported; however, metachronous intracranial double tumors induced by radiation therapy are extremely rare. A 1-year-old boy had undergone tumor removal and craniospinal radiation therapy (30 Gy) for cerebellar medulloblastoma. At 24 years old, parasagittal meningioma developed in the left parietal region and was totally removed. Six years later, an infiltrative tumor was newly found in the right fronto-temporal white matter. The patient underwent stereotactic biopsy, and the tumor was found to be an anaplastic astrocytoma. Chromosomal analysis by fluorescence in situ hybridization (FISH) revealed loss of heterozygosity (LOH) of 1p. As the patient had previously had craniospinal irradiation, no additional radiation therapy was delivered. He underwent chemotherapy with temozolomide and the disease is now stable. Since both secondary tumors were located within the area of previous radiation and the patient did not have any genetic disease predisposing him to tumors, radiation therapy was considered to be responsible for their tumorigenesis. To our knowledge, this case is the fourth case of radiation-induced double CNS tumors arising after radiotherapy to be described in the literature. Whenever radiation is administered to children or young adults, careful serial screening studies are needed.

摘要

已有报道多种辐射诱发的肿瘤,包括脑膜瘤、胶质瘤和肉瘤;然而,放射治疗诱发的异时性颅内双肿瘤极为罕见。一名1岁男孩因小脑髓母细胞瘤接受了肿瘤切除及颅脊髓放射治疗(30 Gy)。24岁时,左顶叶区域出现矢状旁脑膜瘤并被完全切除。6年后,在右额颞白质中新发现一个浸润性肿瘤。患者接受了立体定向活检,发现该肿瘤为间变性星形细胞瘤。荧光原位杂交(FISH)染色体分析显示1p杂合性缺失(LOH)。由于患者此前接受过颅脊髓照射,未进行额外的放射治疗。他接受了替莫唑胺化疗,目前病情稳定。由于这两个继发性肿瘤均位于先前放疗区域内,且患者没有任何易患肿瘤的遗传疾病,因此认为放射治疗是其肿瘤发生的原因。据我们所知,该病例是文献中描述的第四例放疗后发生的辐射诱发双中枢神经系统肿瘤。每当对儿童或年轻成人进行放疗时,都需要进行仔细的系列筛查研究。

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