Li-Fraumeni syndrome: Multiple distinct brain tumours in two brothers

被引:0
|
作者
Lechien, J. R. [1 ]
Brotchi, J. [2 ]
Van Maldergem, L. [3 ]
De Araujo, P. Costa [1 ]
Bruninx, G. [4 ]
Hilbert, P. [5 ]
Nubourgh, Y. [6 ]
机构
[1] Univ Mons, Fac Med, Dept Anat, B-7000 Mons, Belgium
[2] Univ Libre Bruxelles, Erasme Hosp, Dept Neurosurg, Brussels, Belgium
[3] Inst Pathol & Genet, Loverval, Belgium
[4] Univ Libre Bruxelles, CHU Charleroi, Dept Radiol, Brussels, Belgium
[5] Inst Pathol & Genet, B-6041 Gosselies, Belgium
[6] Univ Libre Bruxelles, CHU Charleroi, Dept Neurosurg, Brussels, Belgium
关键词
Li-Fraumeni syndrome; p53; Brain; Genetic; Tumour; MUTATIONS;
D O I
10.1016/j.neuchi.2013.11.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Li-Fraumeni syndrome is a rare autosomal dominant cancer-prone condition characterized by the occurrence of a large set of different types of cancer in a patient and their family. A germline disease-causing mutation of the gene encoding the p53 protein is associated with the syndrome. We report on a family in which segregation of a TP53 mutation in two generations was associated with two brain tumours, a leiomyosarcoma and a thyroid carcinoma in four male patients. The main patient presented with seizures revealing several primary brain tumours. We review recent views on its molecular basis and discuss management of the condition as well as a review of the literature. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:51 / 54
页数:4
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