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Confocal neurolasermicroscopy in human brain - perspectives for neurosurgery on a cellular level (including additional comments to this article).

作者信息

Schlosser H-G, Suess O, Vajkoczy P, van Landeghem F K H, Zeitz M, Bojarski C

机构信息

Department of Neurosurgery, Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.

出版信息

Cent Eur Neurosurg. 2010 Feb;71(1):13-9. doi: 10.1055/s-0029-1237735. Epub 2009 Sep 28.

DOI:10.1055/s-0029-1237735
PMID:19787571
Abstract

BACKGROUND

During neurosurgery intraoperative imaging of vital neural structures on a cellular level would facilitate the development of new strategies for diagnosis and treatment. In vivo imaging would permit the detection of the tumour centre and infiltration zone. With targeted biopsies the lesion of interest could be determined before performing the biopsy, facilitating the final pathological diagnosis. In this study we present confocal neurolasermicroscopy as a new method in neurosurgery.

METHODS

A miniaturised confocal neurolasermicroscope (NLM) was used ex vivo immediately after tumour resection of glioblastoma multiforme (GBM). NLM was performed with subcellular magnification up to a tissue depth of 100 microm. NLM images were compared to conventional histological images of the same tumour.

RESULTS

The application of the method in nine patients allowed adequate diagnosis of a malignant glioma fulfilling the WHO criteria when compared to conventional histology. In one patient with glioblastoma multiforme NLM allowed the correct diagnosis of GBM to be made, demonstrating the high mitotic rate and cell pleomorphy of the tumour cells. Additional characteristics such as pleomorphic cells, mitotic figures, fibrillary matrix and the distinction between tumour centre and infiltration zone could be shown.

CONCLUSIONS

NLM is a tool which could be adapted for neurosurgical intraoperative applications with the potential to diagnose tumours and recognise the tumour centre and infiltration zone in vivo. Further applications of NLM to characterise subcellular structures and vascular architecture are possible.

摘要

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