Molecular analysis of astrocytoma associated with turcot syndrome type 1 - Case report

被引:11
作者
Okamoto, H [1 ]
Mineta, T [1 ]
Nakahara, Y [1 ]
Ichinose, M [1 ]
Shiraishi, T [1 ]
Tabuchi, K [1 ]
机构
[1] Saga Med Sch, Dept Neurosurg, Saga 8498501, Japan
关键词
astrocytoma; Turcot syndrome; mismatch repair genes; p53;
D O I
10.2176/nmc.44.124
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A 49-year-old man presented with a brain tumor and colon carcinoma. The patient had been treated under diagnoses of hereditary non-polyposis colorectal cancer syndrome and Muir-Torre syndrome. Magnetic resonance imaging revealed a mass lesion in the right frontal lobe with diffuse high intensity on T-2-weighted and fluid-attenuated inversion recovery images. A few small lesions were enhanced by gadolinium on the T-1-weighted images. Histological examination revealed the brain neoplasm was astrocytoma grade III according to the World Health Organization classification. Molecular genetic analysis detected microsatellite instability and p53 mutation only in the tumor tissue, indicating a failure of the deoxyribonucleic acid mismatch repair system. These results suggest that inactivation of mismatch repair system and p53 is closely associated with the tumorigenesis of this neoplasm. The final diagnosis was Turcot syndrome type 1.
引用
收藏
页码:124 / 128
页数:5
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