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Seeing Beyond the Lesion: Disease Recognition from Reactive CNS Tissue

Research Medical/Healthcare AI

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TL;DR - Weakly supervised pathology models can predict underlying CNS diseases from reactive, non-lesional biopsy tissue after controlling for sampling-related shortcuts. The findings suggest conventionally non-diagnostic tissue contains subtle disease signals and highlight provenance-only baselines as essential controls.

  • Four pathology foundation models were evaluated as frozen patch encoders on 245 whole-slide images from 186 patients.
  • Coarse disease categories were largely predictable from slide size, exposing a major acquisition confound.
  • For three finer diagnostic distinctions, predictions remained above chance after removing this confound (permutation testing, p ≤ 10⁻⁴).
  • Performance did not significantly differ among the four encoders; contribution maps and expert review assessed whether signals arose from reactive tissue rather than artifacts such as blood.

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Seeing Beyond the Lesion: Disease Recognition from Reactive CNS Tissue

arXiv eess.IV Jan Schnorrenberg, Jan Ernsting, Enrico Küllenberg, Tim Hahn, Benjamin Risse, Christian Thomas 2026-09-02 arXiv:2609.02390
Public signals Semantic Scholar citations 0 · Semantic Scholar influential citations 0
Providers: Hugging Face · N/A OpenAlex · N/A Publisher · N/A Semantic Scholar · Citations 0 · Influential citations 0 X · N/A Fetched 2026-09-25 14:24:35.669617 UTC

TL;DR - Weakly supervised pathology models can predict underlying CNS diseases from reactive, non-lesional biopsy tissue after controlling for sampling-related shortcuts. The findings suggest conventionally non-diagnostic tissue contains subtle disease signals and highlight provenance-only baselines as essential controls.

  • Four pathology foundation models were evaluated as frozen patch encoders on 245 whole-slide images from 186 patients.
  • Coarse disease categories were largely predictable from slide size, exposing a major acquisition confound.
  • For three finer diagnostic distinctions, predictions remained above chance after removing this confound (permutation testing, p ≤ 10⁻⁴).
  • Performance did not significantly differ among the four encoders; contribution maps and expert review assessed whether signals arose from reactive tissue rather than artifacts such as blood.
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