Related Experiment Video
Updated: May 8, 2026

Analysis of Fluorescent-Stained Lipid Droplets with 3D Reconstruction for Hepatic Steatosis Assessment
Published on: June 2, 2023
Detection of macrovesicular steatosis in hematoxylin and eosin-stained histological images of human livers: A
E Malamutmann1, M Platte2, S Theurer3
1General, Visceral & Transplantation Surgery, University Hospital Essen, Hufelandstr. 55, 45147 Essen, Germany.
Background:
Macrovesicular steatosis (MaS) affects liver transplant outcomes. Traditional visual biopsy assessment is subjective and shows inter-observer variability (weighted κ = 0.595 in our cohort), which complicates allocation and prognostication.
Methods:
We developed a semi-automated image analysis method using HALCON Progress (evaluation license, 2019-2023) to quantify MaS in H&E whole-slide images (WSIs). The pipeline processes native SVS files at full resolution (average runtime 1.26 ± 0.53 min/WSI) without tiling, downsampling, or format conversion. Four shape features (area, roundness, circularity, and compactness) guide classification. Results were compared with three specialized pathologists using Pearson and Spearman correlations.
Results:
Across 129 WSIs (≈52,000 lipid droplets), artificial intelligence-pathologist correlations were statistically significant (Pearson r = 0.526-0.642; Spearman ρ = 0.498-0.615; all p < 0.001; n = 48-95 per pathologist). Correlation with the mean pathologist assessment reached R2 = 0.64 (r = 0.80, ρ = 0.782), within the inter-pathologist range (R2 = 0.34-0.62; weighted κ = 0.595). Using four shape features, the pipeline separates vacuoles from vessels and processing artifacts during interactive review. Processing native SVS at full resolution avoids extra compute while preserving precision.
Conclusions:
The method provides a rapid, objective readout of MaS and performs on par with inter-pathologist agreement (R2 = 0.64 vs. weighted κ = 0.595). It is best used as decision-support that supplies percentages and overlays for expert review. Main limitations are underestimation in severe, confluent steatosis (>30%), limited coverage of microvesicular fat, and single-center validation. Multi-center evidence across scanners and patient groups is still needed before routine use.

