Destroy Me: Automatic Artifact Generation for Histopathology Images

Deep learning's diagnostic utility in pathology is constrained by model vulnerability to real-world data imperfections. While current strategies favor "perfect data" by filtering low-quality regions, which can lead to the loss of valuable diagnostic context, we propose a paradigm shift: engineering models to thrive in imperfect environments using "Destroy Me", a hybrid framework for realistic artifact synthesis and robust data augmentation. Our approach combines Stable Diffusion, fine-tuned to preserve morphological continuity by realistically integrating artifacts with the underlying tissue architecture, with physics-based procedural modeling to synthesize six common artifact types: tissue folds, precipitates, blur, stitching errors, dust, and pen markers. Artifact fidelity is assessed using Kernel Inception Distance (KID) and color Wasserstein distance metrics. Validating this strategy on lung adenocarcinoma pattern classification with an nnU-Net, we confirm that models trained on "destroyed" patches consistently outperform baselines on independent real-world datasets. Specifically, we observed a 10.5% relative improvement in macro F1-score and a 15% relative increase in the Cohen's Kappa ($κ$) coefficient. Crucially, our results demonstrate that selective, impact-weighted augmentation is vital for balancing practical robustness with the preservation of subtle diagnostic features.

Deep Learning Segmentation of Diffusion-Weighted MRI Acute Ischaemic Stroke: A Pragmatic Evaluation Across Three Datasets

Objective: Diffusion-weighted MRI (DWI-MRI) is the gold standard for visualizing and quantifying acute ischaemic stroke (AIS). Although deep learning methods can accurately segment AIS lesions, the optimal image inputs and model architecture remain uncertain. We evaluated whether accurate AIS lesion segmentation can be achieved using a pragmatic deep learning approach with minimal preprocessing and clinically feasible inference times. Materials and Methods: Self-configured nnU-Net models were trained on 1,744 DWI cases from local, national, and open-access datasets and tested on 436 cases. Four experimental conditions were evaluated using five-fold cross-validation: with or without brain extraction and using either DWI alone or DWI plus apparent diffusion coefficient (ADC) images as inputs. Two architectures were compared: the baseline nnU-Net (base) and a residual encoder nnU-Net (ResEnc). Performance was benchmarked against the DeepISLES ensemble model from the 2022 ISLES challenge. Results: In the test set (n=436), the base model achieved a median (IQR) Dice similarity coefficient (DSC) of 0.84 (0.19). For the base model, only two of six pairwise comparisons between input configurations showed significant differences. ResEnc produced small but significant improvements in DSC compared with the base model for DWI, DWI+brain extraction, and DWI+ADC inputs (all p<0.02), but not for DWI+ADC+brain extraction (p>0.50). The base model significantly outperformed DeepISLES, particularly in patients with smaller infarct volumes (signed-rank test, p<0.01). Conclusions: A baseline nnU-Net trained on DWI alone, without preprocessing, enabled fast and accurate AIS lesion segmentation. This streamlined approach may facilitate clinical research and support acute stroke imaging workflows

MNet++: Extended 2D/3D Networks for Anisotropic Medical Image Segmentation

This work demonstrates a full reproduction and extension of MNet, a hybrid 2D/3D convolutional network designed for anisotropic medical image segmentation. The original architecture was re-implemented within the nnU-Net framework to verify its reported performance and robustness to variable voxel spacing, known as anisotropy. Experiments were conducted on PROMISE prostate MRI and a controlled subset of LiTS liver CT under matched preprocessing and compute constraints. The reproduced MNet achieved a Dice similarity coefficient (DSC) of 89.0 +/- 0.9% on PROMISE, within 0.8% of the published result, and 94.3 +/- 1.9% / 54.6 +/- 3.1% for liver and tumor segmentation on LiTS, respectively. Two lightweight extensions were further introduced: (1) a learned Fusion Gating mechanism enabling adaptive 2D-3D feature blending, and (2) a VMamba state-space module for efficient long-range depth modelling. The Spatial Gating variant improved DSC by +0.8% with less than 3% inference overhead, while VMamba improved performance consistency, reducing PROMISE Dice variation to +/- 0.7% and achieving the strongest LiTS liver performance at 95.8% Dice. Both extensions preserved MNet robustness to anisotropy, with delta Dice = 1.5% across 1-4 mm voxel spacing. Overall, the study confirms MNet reproducibility and demonstrates that adaptive fusion and state-space modelling have the potential to further strengthen segmentation reliability under anisotropic conditions. However, further tests are required to provide definitive conclusions.