Meningioma 40 years after radiation therapy for retinoblastoma: genetic and phenotypic analysis, and minireview of literature.

Zentralblatt Fur Neurochirurgie Pub Date : 2008-11-01 Epub Date: 2008-07-29 DOI:10.1055/s-2008-1077079
V Balik, M Sarissky, D Lohmann, I Sulla
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引用次数: 3

Abstract

The authors present a case of 44-year-old Caucasian female diagnosed with meningothelial meningioma 40 years after radiotherapy for sporadic unilateral retinoblastoma. The genetic analysis of DNA from the meningioma revealed no oncogenic mutation in the RB1 gene. The analysis of meningioma cells by flow cytometry revealed the following immunophenotype: vimentin++ CD56+ GFAP- EGFR-. Intermediate intensities of Her-2/neu and Pgp expression were detected in a small percentage of tumour cells. Data suggest that the tumour was most likely induced by radiotherapy and did not arise as a second tumour as there was no hereditary predisposition to retinoblastoma.

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视网膜母细胞瘤放射治疗后40年脑膜瘤:遗传和表型分析,以及文献综述。
作者报告一例44岁的高加索女性,在散发性单侧视网膜母细胞瘤放疗40年后被诊断为脑膜上皮脑膜瘤。脑膜瘤DNA的遗传分析显示,RB1基因没有致癌突变。流式细胞术分析脑膜瘤细胞的免疫表型为:vimentin++ CD56+ GFAP- EGFR-。在一小部分肿瘤细胞中检测到中等强度的Her-2/neu和Pgp表达。数据显示,该肿瘤很可能是由放疗引起的,由于没有视网膜母细胞瘤的遗传倾向,因此没有作为第二肿瘤出现。
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Zentralblatt Fur Neurochirurgie
Zentralblatt Fur Neurochirurgie 医学-神经科学
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Persistent cerebrospinal fluid rhinorrhea by intrasphenoidal encephalocele. Lumbar spinal osteoblastoma mimicking a dumbbell radicular schwannoma. Hemorrhage into cystic vestibular schwannoma following stereotactic radiation therapy. Meningioma 40 years after radiation therapy for retinoblastoma: genetic and phenotypic analysis, and minireview of literature. Spheno-orbital meningiomas: surgical approaches and outcome according to the intraorbital tumor extent.
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