10094-MPC-8 小儿小脑髓母细胞瘤治疗后辐射诱发胶质母细胞瘤的分子病理分析

N. Ohe, Takafumi Okubo, Kenji Shoda, Tetsuya Yamada, N. Suzui, N. Nakayama, Tatsuhiko Miyazaki
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摘要

摘要:由于治疗方案的改进,儿童成神经管细胞瘤的长期幸存者数量一直在增加。然而,继发性癌症对长期幸存者来说可能是一个问题。我们报告两例放射诱导的胶质母细胞瘤的分子病理学评价。患者:在本院治疗的27例小脑髓母细胞瘤患者中,2例确诊时分别为3岁和11岁,均为女孩,初次治疗后分别在5岁11个月和22岁8个月发生小脑胶质母细胞瘤。这两例小脑胶质母细胞瘤临床诊断为放射性继发性肿瘤。结果临床诊断为放射性胶质母细胞瘤的2例患者免疫组化结果均为IDH-1阴性、EGFR阴性、p53阳性。据报道,EGFR表达为阴性是辐射诱导的胶质母细胞瘤的分子特征,我们所经历的两个病例与辐射诱导的继发性癌症一致。一般情况下,原发性胶质母细胞瘤的幕上区EGFR表达阳性,幕下区EGFR表达阴性。因此,在幕上胶质母细胞瘤的病例中,评估EGFR表达对于区分原发性胶质母细胞瘤和继发性胶质母细胞瘤是有用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
10094-MPC-8 MOLECULAR PATHOLOGICAL ANALYSIS OF RADIATION-INDUCED GLIOBLASTOMA AFTER PEDIATRIC CEREBELLAR MEDULLOBLASTOMA TREATMENT
Abstract INTRODUCTION The number of long-term survivors of pediatric medulloblastoma has been increasing due to improved treatment options. However, secondary cancer can be an issue for long-term survivors. We report the molecular pathological evaluation of two cases of radiation-induced glioblastoma. Patients: Of the 27 patients with cerebellar medulloblastoma treated at our institution, two who were 3 years old and 11 years old at the time of medulloblastoma diagnosis and both were girls, developed cerebellar glioblastomas after the initial treatment at five years and 11 months and 22 years and eight months, respectively. These two cerebellar glioblastomas were clinically diagnosed as radiation-induced secondary cancer. RESULTS Both of the two cases we clinically diagnosed as radiation-induced glioblastoma had negative IDH-1, EGFR expression and positive p53 expression in immunohistochemistry. DISCUSSION It has been reported that EGFR expression is negative as a molecular feature of radiation-induced glioblastoma, and the two cases we experienced were consistent with radiation-induced secondary cancers. In general, primary glioblastoma is positive for EGFR expression in the supratentorial region and negative in the infratentorial region. Therefore, in the case of supratentorial glioblastoma, it is useful to evaluate EGFR expression to distinguish primary glioblastoma from secondary glioblastoma.
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