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儿童髓母细胞瘤治疗后放射性非典型脑膜瘤的细胞遗传学发现:病例报告及文献复习。

Cytogenetic findings in pediatric radiation-induced atypical meningioma after treatment of medulloblastoma: case report and review of the literature.

机构信息

Laboratório de Pediatria, Division of Pediatric Oncology, Department of Pediatrics, Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto, University of São Paulo, Bloco G. Av. Bandeirantes, Bairro Monte Alegre 3900, Ribeirão Prêto, SP, CEP 14048-900, Brazil.

出版信息

J Neurooncol. 2012 Dec;110(3):397-402. doi: 10.1007/s11060-012-0982-5. Epub 2012 Oct 18.

Abstract

Ionizing radiation is the most recognized risk factor for meningioma in pediatric long-term cancer survivors. Information in this rare setting is exceptional. We report the clinical and cytogenetic findings in a radiation-induced atypical meningioma following treatment for desmoplastic medulloblastoma in a child. This is the second study to describe the cytogenetic aspects on radiation-induced meningiomas in children. Chromosome banding analysis revealed a 46, XX, t(1;3)(p22;q12), del(1)(p?)[8]/46, XX[12]. Loss of chromosome 1p as a consequence of irradiation has been proposed to be more important in the development of secondary meningiomas in adults. Deletions in the short arm of chromosome 1 also appear to be a shared feature in both pediatric cases so far analyzed.

摘要

电离辐射是儿科长期癌症幸存者中脑膜瘤最公认的危险因素。在这种罕见的情况下,信息是特殊的。我们报告了一例儿童促结缔组织增生型髓母细胞瘤治疗后发生的放射性非典型脑膜瘤的临床和细胞遗传学发现。这是第二例描述儿童放射性脑膜瘤细胞遗传学方面的研究。染色体带分析显示 46,XX,t(1;3)(p22;q12),del(1)(p?)[8]/46,XX[12]。据推测,照射后 1 号染色体短臂缺失在成人继发性脑膜瘤的发生中更为重要。到目前为止,在分析的两个儿科病例中,1 号染色体短臂缺失似乎也是一个共同特征。

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