Diverse molecular pattern in a bihemispheric glioblastoma (butterfly glioma) in a 16-year-old boy

被引:13
作者
Zakrzewska, Magdalena
Szybka, Malgorzata
Zakrzewski, Krzysztof
Biernat, Wojciech
Kordek, Radzislaw
Rieske, Piotr
Golanska, Ewa
Zawlik, Izabela
Piaskowski, Sylwester
Liberski, Pawel P.
机构
[1] Med Univ Lodz, Dept Mol Pathol & Neuropathol, Chair Oncol, PL-92216 Lodz, Poland
[2] Med Univ Lodz, Dept Pathol & Oncol, Chair Oncol, PL-93509 Lodz, Poland
[3] Med Univ Lodz, Dept Pediat Neurosurg, Chair Pediat Neurosurg & Neurol, PL-93338 Lodz, Poland
[4] Med Univ Gdansk, Dept Neuropathol & Mol Pathol, PL-80210 Gdansk, Poland
关键词
D O I
10.1016/j.cancergencyto.2007.04.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Glioblastoma multiforme (GBM), the most common malignant brain tumor of adults, is relatively rare in children. In a GBM affecting a 16-year-old boy, the tumor spread across the corpus callosum (butterfly glioma). This type of bilateral hemispheric growth has previously been thought to result from spread along the white matter tracts. Two samples obtained from opposite sides of the same tumor were analyzed comprehensively for loss of heterozygosity (LOH) and microsatellite instability (MSI). Amplification of EGFR and MDM2 was studied by means of multiplex polymerase chain reaction. Exons 5, 6, 7, and 8 of TP53 were screened for mutations by sequencing. In neither specimen were molecular alterations found in the EGFR, MDM2, or TP53 genes. The specimen obtained from the right hemisphere exhibited a high level of NISI and LOH in chromosome arms 5q, 9p, and 13q. The specimen from the left hemisphere exhibited LOH in chromosome arms 3p, 5q, 9p, 9q, 10p, 10q, and l3q. Here we propose four plausible hypothetical scenarios underlying the tumorigenesis of this G13M. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
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