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Li-Fraumeni syndrome: multiple distinct brain tumours in two brothers.
Lechien, J R; Brotchi, J; Van Maldergem, L; Costa de Araujo, P; Bruninx, G; Hilbert, P; Nubourgh, Y.
Affiliation
  • Lechien JR; Department of Anatomy, Faculty of Medicine, University of Mons, avenue du Champ-de-Mars, 6, 7000 Mons, Belgium. Electronic address: Jerome.lechien@ulb.ac.be.
  • Brotchi J; Department of Neurosurgery, Erasme Hospital, Université Libre de Bruxelles, Bruxelles, Belgium.
  • Van Maldergem L; Institute of Pathology and Genetics, Loverval, Belgium.
  • Costa de Araujo P; Department of Anatomy, Faculty of Medicine, University of Mons, avenue du Champ-de-Mars, 6, 7000 Mons, Belgium.
  • Bruninx G; Department of Radiology, CHU Charleroi, Université Libre de Bruxelles, Bruxelles, Belgium.
  • Hilbert P; Institute of Pathology and Genetics, avenue Georges-Lemaître, 25, 6041 Gosselies, Belgium.
  • Nubourgh Y; Department of Neurosurgery, CHU Charleroi, Université Libre de Bruxelles, Bruxelles, Belgium.
Neurochirurgie ; 60(1-2): 51-4, 2014.
Article in En | MEDLINE | ID: mdl-24636404
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Genes, p53 / Li-Fraumeni Syndrome / Mutation Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: Neurochirurgie Year: 2014 Document type: Article Country of publication: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Genes, p53 / Li-Fraumeni Syndrome / Mutation Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: Neurochirurgie Year: 2014 Document type: Article Country of publication: France