医学
银屑病
背景(考古学)
人工智能
特征(语言学)
皮肤病科
队列
卷积神经网络
皮肤损伤
诊断准确性
组织病理学
机器学习
模式识别(心理学)
深度学习
特征向量
计算机科学
基线(sea)
作者
Luis Carlos Rivera Monroy,Anne Petzold,Melissa Indah Sari,Katharina Breininger,Andreas Maier,Julio Vera-Gonzalez,Michael Erdmann,Stefan Schliep,Konstantin Drexler,Dennis Niebel,Stephan Schreml,Kinan Maurice Hayani,Valentin Aebischer,Stephan A. Braun,Paul Schmidle,Dieter Metze,Michael Sticherling,Carola Berking,Elias A. T. Koch,Markus Vincent Heppt
标识
DOI:10.1007/s00428-026-04445-x
摘要
Psoriasis and eczema are chronic inflammatory skin diseases with overlapping histopathological features, which often lead to diagnostic uncertainty even among experienced dermatopathologists. To address this challenge, we developed a computer-assisted diagnostic framework that combines the Virchow foundation model, pretrained on 1.5 million whole-slide images, with multi-instance learning (MIL) to classify psoriasis and eczema from digitized histopathology slides. Using an internal dataset (n = 40) and an external validation cohort (n = 40), equally balanced between both conditions and annotated by board-certified dermatopathologists, our best-performing configuration (Virchow + CLAM) achieved 85% accuracy, a macro-averaged F1 score of 0.80, and an AUC of 0.81 on the external cohort. This substantially outperformed baseline convolutional neural networks, which reached 61% accuracy, and models relying solely on pretrained feature extractors without MIL, which achieved an average accuracy of 68.8%. In a reader study on the same external cohort, individual dermatopathologist accuracies ranged from 47.5 to 70.0%, with a majority-vote consensus accuracy of 62.5%; our method outperformed both the average individual reader and the consensus under histology-only conditions. Furthermore, the model generates attention heatmaps that provide supportive visual context by highlighting regions associated with model predictions. Importantly, this study is designed as a methodological proof-of-concept conducted under controlled, histology-only conditions and is not intended for direct clinical deployment. Rather than demonstrating clinical readiness, it illustrates the potential of domain-specific foundation models combined with MIL for addressing diagnostically challenging inflammatory dermatoses.
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