đ¤ AI Summary
Cell/nucleus segmentation in histopathological images suffers from severe annotation scarcityâparticularly for rare morphologiesâhindering robust model training.
Method: We propose a novel multimodal conditional diffusion model that jointly integrates morphological maps (horizontal/vertical), RGB color features, and BERT-encoded textual metadata via multi-head cross-attention, enabling fine-grained, controllable image-mask pair generation.
Contribution/Results: The method supports task-oriented data augmentation by synthesizing pixel-accurate, high-fidelity masks whose embedded feature distributions closely match those of real data (low Wasserstein distance). Experiments demonstrate substantial improvements in segmentation generalizationâespecially for underrepresented cell types such as columnar cellsâvalidating the efficacy and novelty of multimodal conditional generation for computational pathology data augmentation.
đ Abstract
Scarcity of annotated data, particularly for rare or atypical morphologies, present significant challenges for cell and nuclei segmentation in computational pathology. While manual annotation is labor-intensive and costly, synthetic data offers a cost-effective alternative. We introduce a Multimodal Semantic Diffusion Model (MSDM) for generating realistic pixel-precise image-mask pairs for cell and nuclei segmentation. By conditioning the generative process with cellular/nuclear morphologies (using horizontal and vertical maps), RGB color characteristics, and BERT-encoded assay/indication metadata, MSDM generates datasests with desired morphological properties. These heterogeneous modalities are integrated via multi-head cross-attention, enabling fine-grained control over the generated images. Quantitative analysis demonstrates that synthetic images closely match real data, with low Wasserstein distances between embeddings of generated and real images under matching biological conditions. The incorporation of these synthetic samples, exemplified by columnar cells, significantly improves segmentation model accuracy on columnar cells. This strategy systematically enriches data sets, directly targeting model deficiencies. We highlight the effectiveness of multimodal diffusion-based augmentation for advancing the robustness and generalizability of cell and nuclei segmentation models. Thereby, we pave the way for broader application of generative models in computational pathology.