Ex vivo fluorescence confocal microscopy: chances and changes in the analysis of breast tissue

Diagn Pathol. 2022 Jun 28;17(1):55. doi: 10.1186/s13000-022-01240-5.

Abstract

Background: Rapid histologic diagnosis of frozen sections is essential for a variety of surgical procedures. Frozen sections however, require specialized lab equipment, are prone to freezing artifacts and are not applicable to all types of tissue. Adipose tissue is especially difficult to process in frozen sections. Although these limitations are well known, no alternative method for microscopic tissue analysis that might replace frozen sections could be established. Our objective was to evaluate whether tissue imaging based on ex vivo fluorescent confocal microscopy (FCM) is applicable for rapid microscopic assessment of breast tumors specimens with abundant adipose tissue.

Methods: We evaluated 17 tissue samples from mastectomy specimens, rich in adipose tissue, submitted to the department of pathology at the Medical University of Vienna. We conducted our study on the FCM VivaScope® 2500M-G4 (Mavig GmbH, Munich, Germany; Caliber I.D.; Rochester NY, USA).

Results: When comparing FCM to frozen sections, we found a very similar overall processing time for FCM images and frozen sections respectively. Image quality was mostly superior to frozen sections (especially for adipose tissue and nuclear detail) but inferior to H&E stained FFPE sections. Limitations of the technology were uneven coloring, invisibility of ink applied for marking tissue margins and distortion artifacts if too much pressure is applied to the tissue.

Conclusion: FCM has the potential to expand the application and usefulness of rapid tissue analysis as speed is comparable and quality exceeds that of frozen sections especially in tissues rich in adipose cells such as breast specimen.

Keywords: Digital Pathology; Ex vivo fluorescence confocal microscopy; Frozen Sections; Gynecopathology.

MeSH terms

  • Breast Neoplasms* / diagnostic imaging
  • Female
  • Frozen Sections
  • Humans
  • Mastectomy
  • Microscopy, Confocal / methods
  • Microscopy, Fluorescence / methods