# The feasibility and accuracy of real-time intra-operative confocal tissue diagnosis in brain and spine cancer surgery

**Authors:** William S. Bolton, Oluwaseyi Adebola, Piravin K. Ramakrishnan, Dharsshini Reveendran, Vassili Crispi, Richard Digby, Rohitashwa Sinha, Arundhati Chakrabarty, Ryan K. Mathew

PMC · DOI: 10.1007/s10143-025-04083-y · 2026-02-17

## TL;DR

This study evaluates a fast confocal microscope for real-time brain and spine tumor diagnosis during surgery, showing promising results for quick and accurate intraoperative decisions.

## Contribution

The study introduces and validates the use of an ultra-fast confocal scanner for real-time intraoperative tissue diagnosis in brain and spine cancer surgery.

## Key findings

- 94% of 47 tissue specimens produced interpretable images within 60 seconds using the Histolog® system.
- Histolog® matched gold standard diagnoses in 68% of cases, comparable to existing intraoperative methods.
- The system enabled real-time tumor cell identification in all specimens.

## Abstract

Real-time intra-operative brain tumour tissue analysis can reduce turnaround times and enable repeated sampling, enhancing diagnostic accuracy and guiding resection. We investigated the use of an ultra-fast confocal microscopy scanner (Histolog®, SamanTree Medical SA) for real-time brain tumour tissue diagnosis. This study aims to demonstrate Histolog®’s diagnostic accuracy in a cohort of brain or spinal cord tumour patients. A single-group, observational study included adult patients undergoing tissue biopsies or tumour debulking surgery. Multiple, freshly excised tissue samples were stained and imaged within 60 seconds using Histolog® alongside standard diagnostic methods. A Consultant Neuropathologist performed a blinded concordance analysis. Of 47 specimens, 94% produced interpretable images during surgery. Histolog® images enabled real-time tumour cell identification in all specimens and matched gold standard diagnoses in 68% of cases. Histolog® demonstrated rapid intraoperative imaging with diagnostic performance for tumour presence that was comparable to existing intraoperative methods in this small cohort, while exact histological concordance was lower (68%). Future studies will explore real-time margin zone analysis and machine learning for automatic diagnosis.

## Linked entities

- **Diseases:** brain tumour (MONDO:0021211), spinal cord tumour (MONDO:0021234)

## Full-text entities

- **Diseases:** glioma (MESH:D005910), prostate cancer (MESH:D011471), pituitary adenoma (MESH:D010911), CNS cancer (MESH:D009369), spinal tumour (MESH:D013125), metastatic (MESH:D000092182), schwannoma (MESH:D009442), neurological deficit (MESH:D009461), RD (MESH:D000077733), AC (MESH:D055577), metastasis (MESH:D009362), meningioma (MESH:D008579), CNS tumour (MESH:D016543), brain or spinal cord tumour (MESH:D013120), lymphoma (MESH:D008223), glioblastoma (MESH:D005909), Brain Tumour (MESH:D001932)
- **Chemicals:** Acridine Orange (MESH:D000165), paraffin (MESH:D010232), FDA 510(k) (-), H&amp;E (MESH:D006371)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909334/full.md

---
Source: https://tomesphere.com/paper/PMC12909334