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小儿接受治疗性颅脑照射后发生的脑肿瘤新生。

De novo formation of brain tumors in pediatric population following therapeutic cranial irradiation.

作者信息

Bilginer Burcak, Türk Cezmi Cagrı, Narin Fırat, Hazer Burcu, Hanalioglu Sahin, Oguz Kader Karlı, Soylemezoglu Figen, Akalan Nejat

机构信息

Department of Neurosurgery, Hacettepe University School of Medicine, Sıhhıye, Ankara, Turkey,

出版信息

Childs Nerv Syst. 2015 Jun;31(6):893-9. doi: 10.1007/s00381-015-2689-3. Epub 2015 Apr 2.

Abstract

PURPOSE

Tumors of central nervous system (CNS) are accounted as the second most common tumors in childhood (21% of all cancers) following hematologic malignancies. The patients can suffer more than one cancer in their lifetime, and radiotherapy is claimed for de novo formation of a new tumor in years after treatment of an initial tumor.

METHODS

We have retrospectively analyzed our database for defining radiotherapy-related de novo brain tumors operated in between January, 2000 and August, 2012. New tumors in the field of radiotherapy were included into the study.

RESULTS

The retrospective analysis revealed six patients (two girls and four boys) eligible for further evaluation. The children were irradiated at an age in the range of 5 and 12 years (mean, 7.8). The primary diagnoses were hematological malignancies in two (acute lymphocytic leukemia and non-Hodgkin lymphoma (NHL)) and solid tumors in other four (two pilocytic astrocytoma, one craniopharyngioma, and one grade 3 astrocytoma). All patients received cranial radiotherapy. The mean latency period for the "second tumor" was 9.5 years. The pathological diagnoses for de novo new tumors were as follows: glial tumor (two cases), medulloblastoma (two cases), mesenchymal tumor (one case), and meningeal sarcoma (one case). All de novo tumors were high graded. Mean survival was 14.6 months.

CONCLUSIONS

de novo brain tumors after irradiation has poor prognosis in neurosurgical practice. Vigilance and awareness for possibility of de novo new tumor are warranted for both families and physicians at follow-ups even years after the treatment of initial tumors.

摘要

目的

中枢神经系统(CNS)肿瘤是儿童期第二常见的肿瘤(占所有癌症的21%),仅次于血液系统恶性肿瘤。患者一生中可能患不止一种癌症,放疗被认为会在初始肿瘤治疗后的数年引发新肿瘤的形成。

方法

我们回顾性分析了2000年1月至2012年8月期间接受手术治疗的放疗相关新发脑肿瘤的数据库。放疗区域内的新肿瘤被纳入研究。

结果

回顾性分析发现6例患者(2名女孩和4名男孩)符合进一步评估条件。这些儿童接受放疗时的年龄在5至12岁之间(平均7.8岁)。原发诊断为血液系统恶性肿瘤的有2例(急性淋巴细胞白血病和非霍奇金淋巴瘤(NHL)),其他4例为实体瘤(2例毛细胞型星形细胞瘤、1例颅咽管瘤和1例3级星形细胞瘤)。所有患者均接受了颅脑放疗。“第二肿瘤”的平均潜伏期为9.5年。新发肿瘤的病理诊断如下:胶质瘤(2例)、髓母细胞瘤(2例)、间叶组织肿瘤(1例)和脑膜肉瘤(1例)。所有新发肿瘤均为高级别。平均生存期为14.6个月。

结论

在神经外科实践中,放疗后新发脑肿瘤预后较差。即使在初始肿瘤治疗数年之后的随访中,患者家属和医生也应警惕新发肿瘤的可能性。

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