AI Article Synopsis

  • Diagnosing malignant skin tumors is difficult due to their confusing visual features, necessitating a more precise approach that utilizes diverse clinical data sources, including images and patient history.
  • The proposed model, Remix-Former++, integrates three branches that focus on clinical images, dermoscopy images, and patient metadata, improving accuracy in identifying skin tumors through specialized attention techniques.
  • With impressive results, including a 5.3% increase in F1 score and 92.6% overall classification accuracy on a large dataset, this model shows potential for practical use in clinical settings, outperforming both previous methods and expert dermatologists.

Article Abstract

Diagnosing malignant skin tumors accurately at an early stage can be challenging due to ambiguous and even confusing visual characteristics displayed by various categories of skin tumors. To improve diagnosis precision, all available clinical data from multiple sources, particularly clinical images, dermoscopy images, and medical history, could be considered. Aligning with clinical practice, we propose a novel Transformer model, named Remix-Former++ that consists of a clinical image branch, a dermoscopy image branch, and a metadata branch. Given the unique characteristics inherent in clinical and dermoscopy images, specialized attention strategies are adopted for each type. Clinical images are processed through a top-down architecture, capturing both localized lesion details and global contextual information. Conversely, dermoscopy images undergo a bottom-up processing with two-level hierarchical encoders, designed to pinpoint fine-grained structural and textural features. A dedicated metadata branch seamlessly integrates non-visual information by encoding relevant patient data. Fusing features from three branches substantially boosts disease classification accuracy. RemixFormer++ demonstrates exceptional performance on four single-modality datasets (PAD-UFES-20, ISIC 2017/2018/2019). Compared with the previous best method using a public multi-modal Derm7pt dataset, we achieved an absolute 5.3% increase in averaged F1 and 1.2% in accuracy for the classification of five skin tumors. Furthermore, using a large-scale in-house dataset of 10,351 patients with the twelve most common skin tumors, our method obtained an overall classification accuracy of 92.6%. These promising results, on par or better with the performance of 191 dermatologists through a comprehensive reader study, evidently imply the potential clinical usability of our method.

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Source
http://dx.doi.org/10.1109/TMI.2024.3441012DOI Listing

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