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71. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
9. Joint Meeting mit der Japanischen Gesellschaft für Neurochirurgie

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

21.06. - 24.06.2020

Confocal laser endomicroscopy – a histological work-up of rare tumours

Konfokale Laserendomikroskopie – eine histologische Gegenüberstellung seltener Tumore

Meeting Abstract

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  • presenting/speaker David Breuskin - Universitätsklinikum des Saarlandes, Klinik für Neurochirurgie, Homburg, Deutschland
  • Joachim Oertel - Universitätsklinikum des Saarlandes, Klinik für Neurochirurgie, Homburg, Deutschland

Deutsche Gesellschaft für Neurochirurgie. 71. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 9. Joint Meeting mit der Japanischen Gesellschaft für Neurochirurgie. sine loco [digital], 21.-24.06.2020. Düsseldorf: German Medical Science GMS Publishing House; 2020. DocP137

doi: 10.3205/20dgnc422, urn:nbn:de:0183-20dgnc4228

Published: June 26, 2020

© 2020 Breuskin et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

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Objective: Confocal laserendomicroscopy (CLE) is a novel investigational technique in neurosurgery. Since the clarification of tumour histology during surgery can be crucial, neurosurgeons need to rely on frozen sections in order to gain a first evaluation. Confocal laserendomicroscopy allows neurosurgeons to evaluate tissue on a microscopic level and gain first estimates of what tumour entity is present. While we have already presented data on more common tumour entities, we aim at providing information on tumours that are rarer and could pose more difficulties for evaluation.

Methods: We have investigated 306 cases of CNS tumours with CLE. Of these, we present cases of the rarer tumor types, namely paraganglioma (n=1), pituitary adenoma (n=7), AVM (n=2), cavernoma (n=4), lymphoma (n=4), plexuspapilloma (n=1), gliosarcoma (n=1) and neuroblastoma (n=1) together with the histological work up in order to make this technology more comprehensible as well as more approachable.

Results: We were able to compare confocal laserendomicroscopic data with histological HE stained specimen in order to evaluate the images. Our work up highlights the specific characteristics of these different tumour typess and draws parallels in order to make the correct diagnostic choice.

Conclusion: Confocal laserendomicroscopy can help neurosurgeons to acquire first information on tumour entities before frozen sections are available. As soon as some knowledge and experience are acquired, CLE may become a strong complementary tool for neurooncological surgery.