Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Sep 1;29(9):940-951.
doi: 10.1097/LVT.0000000000000142. Epub 2023 Apr 6.

Fluorescence confocal microscopy on liver specimens for full digitization of transplant pathology

Affiliations

Fluorescence confocal microscopy on liver specimens for full digitization of transplant pathology

Maximilian N Kinzler et al. Liver Transpl. .

Abstract

Fluorescence confocal microscopy (FCM) is a rapidly evolving tool that provides real-time virtual HE images of native tissue. Data about the potential of FCM as an alternative to frozen sections for the evaluation of donor liver specimens are lacking so far. The aim of the current study was to determine the value of FCM in liver specimens according to the criteria of the German Society for Organ Procurement. In this prospective study, conventional histology and FCM scans of 50 liver specimens (60% liver biopsies, 26% surgical specimens, and 14% donor samples) were evaluated according to the German Society for Organ Procurement. A comparison of FCM scans and conventional frozen sections revealed almost perfect levels of agreement for cholangitis (κ = 0.877), fibrosis (κ = 0.843), and malignancy (κ = 0.815). Substantial levels of agreement could be obtained for macrovesicular steatosis (κ = 0.775), inflammation (κ = 0.763), necrosis (κ = 0.643), and steatohepatitis (κ = 0.643). Levels of agreement were moderate for microvesicular steatosis (κ = 0.563). The strength of agreement between frozen sections and FCM was superior to the comparison of conventional HE and FCM imaging. We introduce FCM as a potential alternative to the frozen section that may represent a novel approach to liver transplant pathology where timely feedback is crucial and the deployment of human resources is becoming increasingly difficult.

PubMed Disclaimer

Comment in

References

    1. MAVIG (12/2020) Datasheet VivaScope® 2500M-G4. Accessed June 2022. https://www.vivascope.de/wp-content/uploads/2022/04/DS_VS-2500M-G4_12-20... 9
    1. Titze U, Hansen T, Titze B, Schulz B, Gunnemann A, Rocco B, et al. Feasibility study for ex vivo fluorescence confocal microscopy (FCM) on diagnostic prostate biopsies. Quant Imaging Med Surg. 2021;11:1322–1332.
    1. Cinotti E, Perrot JL, Labeille B, Cambazard F, Rubegni P. Ex vivo confocal microscopy: an emerging technique in dermatology. Dermatol Pract Concept. 2018;8:109–119.
    1. Dobbs J, Krishnamurthy S, Kyrish M, Benveniste AP, Yang W, Richards-Kortum R. Confocal fluorescence microscopy for rapid evaluation of invasive tumor cellularity of inflammatory breast carcinoma core needle biopsies. Breast Cancer Res Treat. 2015;149:303–310.
    1. Mir MC, Bancalari B, Calatrava A, Casanova J, Dominguez Escrig JL, Ramirez-Backhaus M, et al. Ex-vivo confocal fluorescence microscopy for rapid evaluation of renal core biopsy. Minerva Urol Nefrol. 2020;72:109–113.

Publication types

LinkOut - more resources