Nuwan Madusanka, Prathiksha Padmanabha, Kasunika Guruge, Byeong-Il Lee
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引用次数: 0
Abstract
Staining variability in histopathological images compromises automated diagnostic systems by affecting the reliability of computational pathology algorithms. Existing normalization methods prioritize color consistency but often sacrifice critical morphological details essential for accurate diagnosis. This work proposes a novel deep learning framework, integrating enhanced residual learning with multi-scale attention mechanisms for structure-preserving stain normalization. The approach decomposes the transformation process into base reconstruction and residual refinement components, incorporating attention-guided skip connections and progressive curriculum learning. The method was evaluated on the MITOS-ATYPIA-14 dataset containing 1420 paired H&E-stained breast cancer images from two scanners. The framework achieved exceptional performance with a structural similarity index (SSIM) of 0.9663 ± 0.0076, representing 4.6% improvement over the best baseline (StainGAN). Peak signal-to-noise ratio (PSNR) reached 24.50 ± 1.57 dB, surpassing all comparison methods. An edge preservation loss of 0.0465 ± 0.0088 demonstrated a 35.6% error reduction compared to the next best method. Color transfer fidelity reached 0.8680 ± 0.0542 while maintaining superior perceptual quality (FID: 32.12, IS: 2.72 ± 0.18). The attention-guided residual learning framework successfully maintains structural integrity during stain normalization, with superior performance across diverse tissue types, making it suitable for clinical deployment in multi-institutional digital pathology workflows.
组织病理学图像的染色变异性通过影响计算病理学算法的可靠性而危及自动诊断系统。现有的归一化方法优先考虑颜色一致性,但往往牺牲了准确诊断所必需的关键形态学细节。这项工作提出了一种新的深度学习框架,将增强残差学习与多尺度注意机制相结合,用于保持结构的染色归一化。该方法将转换过程分解为基重构和残差细化两个部分,结合了注意引导的跳过连接和渐进式课程学习。该方法在MITOS-ATYPIA-14数据集上进行了评估,该数据集包含来自两台扫描仪的1420对h&e染色的乳腺癌图像。该框架的结构相似指数(SSIM)为0.9663±0.0076,比最佳基线(StainGAN)提高了4.6%。峰值信噪比(PSNR)达到24.50±1.57 dB,优于所有比较方法。边缘保存损失为0.0465±0.0088,与次优方法相比,误差降低了35.6%。色彩传递保真度达到0.8680±0.0542,同时保持了较好的感知质量(FID: 32.12, IS: 2.72±0.18)。注意引导残差学习框架在染色归一化过程中成功地保持了结构完整性,在不同组织类型中具有卓越的性能,使其适合多机构数字病理工作流程的临床部署。
期刊介绍:
Aims
Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal:
● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings.
● Manuscripts regarding research proposals and research ideas will be particularly welcomed.
● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds.
Scope
● Bionics and biological cybernetics: implantology; bio–abio interfaces
● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices
● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc.
● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology
● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering
● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation
● Translational bioengineering