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DSR-VGG: A Lightweight Depthwise Separable Residual VGG Architecture for Nasopharyngeal Histopathological Image Classification.

October 20, 2026pubmed logopapers

Authors

Abdullahi MK,Mansor S,Ahmad Fauzi MF

Affiliations (2)

  • Faculty of Artificial Intelligence and Engineering, Multimedia University (MMU), Cyberjaya 63100, Malaysia.
  • School of Digital Health, KPJ Healthcare University, Nilai 71800, Malaysia.

Abstract

<b>Background/Objectives:</b> Deep convolutional neural networks achieve strong histopathological image-classification performance but often require substantial computational resources. This study proposes DSR-VGG, a lightweight Depthwise Separable Residual VGG architecture for nasopharyngeal histopathological image classification. <b>Methods:</b> DSR-VGG comprises six Depthwise Separable Blocks with residual projection shortcuts, global average pooling, dropout regularization, and a classification layer. An inverse-frequency weighted random sampling strategy was used to address severe class imbalance. The primary evaluation used 88,002 nasopharyngeal histopathology patches from four classes: Normal, lymphoid hyperplasia, nasopharyngeal inflammation, and nasopharyngeal carcinoma. Training was repeated using three random seeds, with supplementary public datasets used to assess cross-dataset architectural robustness. <b>Results:</b> Across three runs, DSR-VGG achieved 99.764 ± 0.049% accuracy, 99.070 ± 0.365% balanced accuracy, and 99.219 ± 0.215% macro-F1. The model contained only 0.528 million parameters, required approximately 0.31 GFLOPs, and achieved 2.38 ms single-image inference latency under the stated GPU benchmarking conditions. Although several baseline architectures achieved marginally higher accuracy, DSR-VGG maintained competitive predictive performance with substantially lower computational complexity. <b>Conclusions:</b> DSR-VGG provides a favorable accuracy-complexity trade-off for histopathological patch classification. However, patient-/WSI-disjoint evaluation, independent multi-center validation, and whole-slide assessment remain necessary before clinical deployment.

Topics

Journal Article

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