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Stream/Area:
-
Subject:
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Paper ID:
IJSREM68502
Volume:
10 |
10 |
Oct 2026
Pages:
1-8
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
School of Computer Science & Engineering
VIT - AP University
School of Computer Science & Engineering
VIT - AP University
School of Computer Science & Engineering
VIT - AP University
School of Computer Science & Engineering
VIT - AP University
School of Computer Science & Engineering
VIT - AP University
Deep-learning systems for skin-lesion screening are usually reported with one aggregate accuracy on one dataset, which says little about how they behave across skin tones, on images from other sources, or on photographs that are not lesions at all. We built DermaScan AI, a web-based pipeline that combines a DermNet-trained ResNet18 pre-filter, a three-tier (benign, monitor, urgent) ResNet18 risk classifier, Grad-CAM ex-planations, and a confidence gate whose threshold depends on the user’s Fitzpatrick skin type. Our questions were how a baseline classifier behaves across skin types, whether a changed training recipe helps, and how far accuracy falls on data from another source. A baseline trained on HAM10000 reached 80.84% vali-dation accuracy but only 44.2–51.9% on held-out Fitzpatrick17k images, depending on skin type. Retraining on HAM10000 plus half of the lesion-relevant Fitzpatrick17k images, with a lower learning rate, a scheduler and rotation augmentation (v3), raised validation accuracy to 88.69% and held-out accuracy to 54.4–74.8%. The gains for types I–V (14.2–25.5 points) exceeded run-to-run variation over three seeds (SD 1.1–2.2 points); the Type VI gain (2.5 points) did not. The gap between the best and worst skin type widened from 7.7 to 20.3 points. On ISIC 2019 images that are not in HAM10000 (n = 2, 403), balanced accuracy was 55.70% against 80.50% on the HAM10000 validation split. The pre-filter reached 86.20% in-domain. Splits are image-level, labels are tiers we derived from dataset diagnoses, no clinician reviewed any output, and the routing rule was not evaluated by risk–coverage analysis, so these results say nothing about clinical safety.
KEYWORDS
We built and measured a two-stage skin-lesion screening pipeline with a skin-type-dependent confidence gate and Grad-CAM explanations. Retraining raised validation accuracy from 80.84% to 88.69% and held-out accuracy for every skin type, with gains for types I–V that exceeded seed variation, but the gap between best and worst skin type grew from 7.7 to 20.3 points, the type VI gain was not distinguishable from noise, and balanced accuracy on ISIC 2019 images outside HAM10000 was 55.70% against 80.50% on the HAM10000 validation split. The gate, pre-filter and explanations work end to end, but their value for safety is unproven. Future work (not completed): split HAM10000 by lesion; compute calibration error for all sets; evaluate the gate with risk–coverage curves; ablate the v3 changes and add a control with skin-type-unbalanced Fitzpatrick17k data; collect more type V–VI images; test on phone photographs; and have der-matologists review the tier mapping and the system’s outputs.
[1] A. Esteva et al., “Dermatologist-level classification of skin cancer with deep neural networks,” Nature, vol. 542, pp. 115–118, 2017. [2] M. Groh et al., “Evaluating deep neural networks trained on clinical images in dermatology with the Fitzpatrick 17k dataset,” in Proc. IEEE/CVF Conf. Comput. Vis. Pattern Recognit. Workshops (CVPRW), 2021, pp. 1820–1828. [3] R. Daneshjou et al., “Disparities in dermatology AI performance on a diverse, curated clinical image set,” Sci. Adv., vol. 8, no. 32, Art. no. eabq6147, 2022. [4] R. R. Selvaraju, M. Cogswell, A. Das, R. Vedantam, D. Parikh, and A. Batra, “Grad-CAM: Visual explanations from deep networks via gradient-based localization,” in Proc. IEEE Int. Conf. Comput. Vis. (ICCV), 2017, pp. 618–626. [5] Y. Geifman and R. El-Yaniv, “Selective classification for deep neural networks,” in Adv. Neural Inf. Process. Syst. (NeurIPS), 2017. [6] P. Tschandl, C. Rosendahl, and H. Kittler, “The HAM10000 dataset, a large collection of multi-source dermatoscopic images of common pigmented skin lesions,” Sci. Data, vol. 5, Art. no. 180161, 2018. [7] N. Codella et al., “Skin lesion analysis toward melanoma detection 2018: A challenge hosted by the International Skin Imaging Collaboration (ISIC),” arXiv:1902.03368, 2019. [8] M. Combalia et al., “BCN20000: Dermoscopic lesions in the wild,” arXiv:1908.02288, 2019. [9] DermNet NZ, “Dermatology image dataset,” https://dermnetnz.org/ dermatology-image-dataset. Accessed: Aug. 18, 2026. [10] C. Vadivelraju, K. E. S., V. M. B. Kumar, P. Suraj, and M. H. Reddy, “DermaScan AI: Deep learning system for preliminary diagnosis of dermatological manifestations,” Int. J. Creative Research Thoughts (IJCRT), 2025, paper IJCRT2505389.
Publication Date
10/30/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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