Holistic and Historical Instance Comparison for Cervical Cell Detection
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Abstract (arXiv)
Cytology screening from Papanicolaou (Pap) smears is a common and effective tool for the preventive clinical management of cervical cancer, where abnormal cell detection from whole slide images serves as the foundation for reporting cervical cytology. However, cervical cell detection remains challenging due to 1) hazily-defined cell types (e.g., ASC-US) with subtle morphological discrepancies caused by the dynamic cancerization process, i.e., cell class ambiguity, and 2) imbalanced class distributions of clinical data may cause missed detection, especially for minor categories, i.e., cell class imbalance. To this end, we propose a holistic and historical instance comparison approach for cervical cell detection. Specifically, we first develop a holistic instance comparison scheme enforcing both RoI-level and class-level cell discrimination. This coarse-to-fine cell comparison encourages the model to learn foreground-distinguishable and class-wise representations. To emphatically improve the distinguishability of minor classes, we then introduce a historical instance comparison scheme with a confident sample selection-based memory bank, which involves comparing current embeddings with historical embeddings for better cell instance discrimination. Extensive experiments and analysis on two large-scale cytology datasets including 42,592 and 114,513 cervical cells demonstrate the effectiveness of our method. The code is available at https://github.com/hjiangaz/HERO.
Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 16 of its 21 references that are in the map. First posted on arXiv 21 Sep 2024.
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References · 16
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- 2023DoNet: Deep De-overlapping Network for Cytology Instance Segmentationcited by 16
- 2021Deep Semi-supervised Metric Learning with Dual Alignment for Cervical Cancer Cell Detectioncited by 6
- 2022Exploring Contextual Relationships for Cervical Abnormal Cell Detectioncited by 1
- 2022Sample hardness based gradient loss for long-tailed cervical cell detectioncited by 1
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