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Management of non-vestibular schwannomas in adult patients: a systematic review and consensus statement on behalf of the EANS skull base section. Part I: oculomotor and other rare non-vestibular schwannomas (I, II, III, IV, VI).

Authors :
Bal J
Bruneau M
Berhouma M
Cornelius JF
Cavallo LM
Daniel RT
Froelich S
Jouanneau E
Meling TR
Messerer M
Roche PH
Schroeder HWS
Tatagiba M
Zazpe I
Paraskevopoulos D
Source :
Acta neurochirurgica [Acta Neurochir (Wien)] 2022 Feb; Vol. 164 (2), pp. 285-297. Date of Electronic Publication: 2021 Nov 09.
Publication Year :
2022

Abstract

Background: Non-vestibular schwannomas are relatively rare, with trigeminal and jugular foramen schwannomas being the most common. This is a heterogeneous group which requires detailed investigation and careful consideration to management strategy. The optimal management for these tumours remains unclear, and there are several controversies. The aim of this paper is to provide insight into the main principles defining management and surgical strategy, in order to formulate a series of recommendations.<br />Methods: A task force was created by the EANS skull base section along with its members and other renowned experts in the field to generate recommendations for the surgical management of these tumours on a European perspective. To achieve this, the task force performed an extensive systematic review in this field and had discussions within the group. This article is the first of a three-part series describing non-vestibular schwannomas (I, II, III, IV, VI).<br />Results: A summary of literature evidence was proposed after discussion within the EANS skull base section. The constituted task force dealt with the practice patterns that exist with respect to pre-operative radiological investigations, ophthalmological assessments, optimal surgical and radiotherapy strategies and follow-up management.<br />Conclusion: This article represents the consensually derived opinion of the task force with respect to the treatment of non-vestibular schwannomas. For each of these tumours, the management of these patients is complex, and for those which are symptomatic tumours, the paradigm is shifting towards the compromise between function preservation and progression-free survival.<br /> (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Details

Language :
English
ISSN :
0942-0940
Volume :
164
Issue :
2
Database :
MEDLINE
Journal :
Acta neurochirurgica
Publication Type :
Academic Journal
Accession number :
34755208
Full Text :
https://doi.org/10.1007/s00701-021-05048-y