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This research addresses cell mimicry in digital pathology by leveraging region-level tissue reasoning propagated via Unbalanced Optimal Transport, effectively bridging the gap between coarse MLLM estimates and fine-grained cellular classification. The proposed Loki-OT framework distills context-aware decision boundaries into a lightweight classifier that outperforms standard fully supervised models on ambiguous epithelium-rich tissues. This advancement represents a significant step forward in machine learning applications for medical imaging, specifically enhancing diagnostic accuracy through improved contextual feature utilization rather than introducing new AI paradigms like quantum computing or general foundation model shifts.
Lymphocyte Mimicry Correction via Region-Level Tissue Reasoning and Unbalanced Optimal Transport
arXiv:2608.17151v1 Announce Type: cross Abstract: Cell mimicry arises when different cell types appear morphologically similar. Human pathologists resolve this ambiguity using surrounding tissue context, whereas current vision models either lack contextual reasoning (cell foundation models) or cannot operate at the cell level (pathology MLLMs). We present Loki-OT, which propagates region-level tissue reasoning to individual cell predictions via Unbalanced Optimal Transport, using MLLM-derived density priors as soft guidance for ambiguous cell reassignment. Loki-OT is motivated by the observation that pretrained cell foundation model features already encode discriminative information, including tissue context, but standard cell-level supervision fails to use tissue context effectively. The resulting transport plan is distilled into a lightweight student MLP classifier that learns context-aware decision boundaries within the pretrained feature space. On the independent TCGA-BRCA cohort, Loki-OT achieved lower patient-level MAE than the fully supervised in-domain PanopTILs classifier and improved F1 in epithelium-rich mimicry tissues, using 278 weak region-level MLLM estimates built on a general-domain cell foundation model. Code: https://github.com/xiangli980/Lymphocyte_Mimicry_Correction_via_Loki_OT
Abstract:Cell mimicry arises when different cell types appear morphologically similar. Human pathologists resolve this ambiguity using surrounding tissue context, whereas current vision models either lack contextual reasoning (cell foundation models) or cannot operate at the cell level (pathology MLLMs). We present Loki-OT, which propagates region-level tissue reasoning to individual cell predictions via Unbalanced Optimal Transport, using MLLM-derived density priors as soft guidance for ambiguous cell reassignment. Loki-OT is motivated by the observation that pretrained cell foundation model features already encode discriminative information, including tissue context, but standard cell-level supervision fails to use tissue context effectively. The resulting transport plan is distilled into a lightweight student MLP classifier that learns context-aware decision boundaries within the pretrained feature space. On the independent TCGA-BRCA cohort, Loki-OT achieved lower patient-level MAE than the fully supervised in-domain PanopTILs classifier and improved F1 in epithelium-rich mimicry tissues, using 278 weak region-level MLLM estimates built on a general-domain cell foundation model. Code: this https URL
13 pages, 3 figures. Accepted to the MICCAI 2026 COMPAYL Workshop
Computer Vision and Pattern Recognition (cs.CV); Machine Learning (cs.LG)
arXiv:2608.17151 [cs.CV]
(or arXiv:2608.17151v1 [cs.CV] for this version)
https://doi.org/10.48550/arXiv.2608.17151 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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Full text under the publisher's open licence · 269 words
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