Role
Co-author
Venue
Scientific Reports, vol. 16 (2026)
Status
Published

The problem

Most computer-assisted diagnostic systems are opaque. A clinician sees a label and a confidence score, with no way to tell how a particular clinical fact — the patient's age, whether the lesion itches, where it is on the body — moved the decision.

That matters practically: a system that cannot show its reasoning cannot be audited, and a system that is confidently wrong is more dangerous than one that says it does not know.

The approach

  1. Image prediction as a prior

    The vision backbone produces an initial distribution over lesion classes. Everything after that is evidence updating rather than a single opaque forward pass.

  2. Stepwise Bayesian updating over clinical features

    Each clinical attribute is incorporated one at a time, so the framework can be evaluated with incrementally available metadata. The intermediate states are the explanation — you can read off which feature moved the posterior and by how much.

  3. Stepwise calibration

    Sequential Bayesian updating compounds overconfidence. The calibration protocol scales with the volume of evidence seen so far, keeping the confidence estimate statistically reliable at every intermediate step, not only at the end.

  4. Validated across backbones and datasets

    Four competitive vision backbones on three datasets, compared against state-of-the-art attention-based multimodal methods.

Results

PAD-UFES-20, peak result across the evaluated backbones.

77.2 ± 3.6 % Balanced accuracy
4 Vision backbones
3 Datasets
≥ attention-based SOTA Comparison

Qualitative case studies show a reasoning process consistent with clinical logic.

Publication & code

Publication

Bouzon, P. H. G., da Rocha, W. F., de Souza, L. A., Pacheco, A. G. C. PRISM: a clinically interpretable stepwise framework for multimodal skin cancer diagnosis. Scientific Reports, vol. 16, 2026.

Related work

Other parts of the same research line.