Literature DB >> 17470137

Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?

D G R Evans1, R T Ramsden, C Gokhale, N Bowers, S M Huson, A Wallace.   

Abstract

Early onset of vestibular schwannoma (VS) is associated with the inherited condition neurofibromatosis type 2 (NF2). However, the majority of NF2 presents bilaterally and the proportion of early-onset apparent sporadic unilateral VS because of NF2 remains to be determined. We have determined the risk by studying NF2 risk in a population-based set of VS, looking at the mode of presentation in a large NF2 data set and the outcome of NF2 mutation analysis in 148 sporadic unilateral VS. The risk of NF2 in an apparently sporadic case of unilateral VS is small apart from in the very youngest age group (<20 years). NF2 germ line mutation testing is unlikely to reveal a mutation except <20 years as a result of the low risk and high rates of mosaicism. Germ line mutation testing is probably only justified in sporadic unilateral VS <20 years unless other features of NF2 are present. Ideally mutation testing should start with the original tumour specimen.

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Year:  2007        PMID: 17470137     DOI: 10.1111/j.1399-0004.2007.00778.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

Review 1.  Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review.

Authors:  Aamira Huq; Maira Kentwell; Amanda Tirimacco; Jacqueline Rossini; Lesley Rawlings; Ingrid Winship
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

2.  Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young Adults.

Authors:  Omar N Pathmanaban; Katherine V Sadler; Ian D Kamaly-Asl; Andrew T King; Scott A Rutherford; Charlotte Hammerbeck-Ward; Martin G McCabe; John-Paul Kilday; Christian Beetz; Nicola K Poplawski; D Gareth Evans; Miriam J Smith
Journal:  JAMA Neurol       Date:  2017-09-01       Impact factor: 18.302

Review 3.  Meningiomas and neurofibromatosis.

Authors:  Stéphane Goutagny; Michel Kalamarides
Journal:  J Neurooncol       Date:  2010-08-17       Impact factor: 4.130

Review 4.  Familial syndromes associated with intracranial tumours: a review.

Authors:  Adrianna M Ranger; Yatri K Patel; Navjot Chaudhary; Ram V Anantha
Journal:  Childs Nerv Syst       Date:  2013-11-06       Impact factor: 1.475

5.  Benign retroperitoneal schwannoma presenting as colitis: a case report.

Authors:  Gary Fass; Didier Hossey; Michel Nyst; Dirk Smets; Esmail-Najar Saligheh; Ruth Duttmann; Kathleen Claes; Pierre-Mendes da Costa
Journal:  World J Gastroenterol       Date:  2007-11-07       Impact factor: 5.742

6.  EANO guideline on the diagnosis and treatment of vestibular schwannoma.

Authors:  Roland Goldbrunner; Michael Weller; Jean Regis; Morten Lund-Johansen; Pantelis Stavrinou; David Reuss; D Gareth Evans; Florence Lefranc; Kita Sallabanda; Andrea Falini; Patrick Axon; Olivier Sterkers; Laura Fariselli; Wolfgang Wick; Joerg-Christian Tonn
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7.  Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene.

Authors:  D Gareth Evans; Andrew J Wallace; Claire Hartley; Simon R Freeman; Simon K Lloyd; Owen Thomas; Patrick Axon; Charlotte L Hammerbeck-Ward; Omar Pathmanaban; Scott A Rutherford; Mark Kellett; Roger Laitt; Andrew T King; Jemma Bischetsrieder; Jaishri Blakeley; Miriam J Smith
Journal:  Laryngoscope       Date:  2018-10-16       Impact factor: 3.325

Review 8.  Neurofibromatosis type 2 (NF2): a clinical and molecular review.

Authors:  D Gareth R Evans
Journal:  Orphanet J Rare Dis       Date:  2009-06-19       Impact factor: 4.123

Review 9.  Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis.

Authors:  Ryota Tamura
Journal:  Int J Mol Sci       Date:  2021-05-29       Impact factor: 5.923

  9 in total

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