arXiv:2608. 11280v1 Announce Type: cross Abstract: Skin cancer diagnosis from dermoscopic images remains challenging due to high intra-class variability, inter-class similarity, class imbalance, and the limited interpretability of deep learning models.
Accurate dermatological diagnosis naturally necessitates equitable performance across diverse populations, yet a systematic lack of expertly annotated images, especially for underrepresented skin tones and rare diseases, impedes progress toward measurably fair methods. We introduce cgDDI (Controllable Generation of Diverse Dermatological Imagery), a hybrid framework that (1) synthesizes realistic healthy skin samples without disturbing other input properties, (2) maps single-sample rare lesions onto novel skin-tones and locations non-parametrically, and (3) allows for efficient parametric generation with as few as 10 training samples.
The study examines why dermatology AI models, largely trained on light‑skinned, cancer‑focused images, perform poorly when applied to diverse patient populations. By comparing a cancer‑trained baseline, two dermatology foundation models, and a general‑purpose vision model on tone‑stratified and disease‑shifted datasets, the authors find that disease‑distribution shift, rather than skin‑tone underrepresentation, is the primary cause of generalization failure. Representation analysis shows that cancer‑specialized features lack transferable structure, while dermatology‑pretrained features maintain stronger clustering, and lightweight adaptation with about ten labeled examples per category can recover most performance.
Skin cancer diagnosis from dermoscopic images remains challenging due to high intra-class variability, inter-class similarity, class imbalance, and the limited interpretability of deep learning models. This paper proposes an uncertainty-aware and explainable deep learning framework for multi-class skin lesion classification.
arXiv:2609.07180v1 Announce Type: cross Abstract: Basal Cell Carcinoma (BCC) is the most common type of skin cancer, accounting for nearly 80% of skin cancer di- agnoses. Its optimal clinical managem...
Background/Objectives: Dermoscopic skin lesion classifiers often lose accuracy under domain shift across imaging devices, illumination, and capture artifacts. We study how data augmentation improves the robustness of a binary malignant-versus-non-malignant classifier, with emphasis on out-of-domain (OOD) generalization.
arXiv:2607. 26765v1 Announce Type: cross Abstract: Background/Objectives: Dermoscopic skin lesion classifiers often lose accuracy under domain shift across imaging devices, illumination, and capture artifacts.
The paper introduces MIFR, a modality‑invariant and fair representation framework for skin disease classification that jointly processes clinical photographs and dermoscopic images using ViT‑based encoders. It employs a five‑component multi‑objective loss to balance classification accuracy, fairness across skin tones, class alignment, and modality invariance. Experiments on paired and external datasets demonstrate competitive predictive performance and fairness, with t‑SNE visualizations confirming alignment of embeddings from different modalities.
The study compares five pre‑trained convolutional neural networks—ResNet50, VGG16, VGG19, MobileNet, and InceptionV3—for melanoma detection using dermatoscopic and histopathological image datasets. Accuracy varied across models and modalities, with ResNet50 achieving the highest scores (84% on HAM10000 and 83% on CR‑AI4SkIN) and InceptionV3 the lowest (71% on ISIC 2018). The results show that a model’s performance on dermatoscopic images does not necessarily predict its performance on histopathological images.
Skin diseases represent a major global public health burden, yet machine learning tools developed to assist in their diagnosis suffer from two critical limitations: reliance on only one modality for d...
CG-HAF is a global‑local fusion framework for ordinal acne severity grading that explicitly combines holistic facial severity probabilities with structured lesion‑burden descriptors such as lesion count, detection confidence, and lesion area. The model uses a lightweight, interpretable classifier to produce the final grade, achieving statistically significant improvements over global‑evidence‑only baselines, especially for severe cases. Cross‑dataset testing reveals that strong performance within a dataset does not automatically transfer, largely due to mismatched grading criteria rather than detection failures.
The paper introduces the Semantic Tri-view Pipeline, an interpretable system that automatically screens teledermatology photographs for gradability by analyzing epidermal micro-relief across up to three smartphone views. It uses a lightweight DeepLabV3+ model to segment micro-relief fidelity and aggregates the resulting spatial masks with logistic regression, leveraging viewpoint redundancy to improve robustness. Evaluated on the SCIN dataset, the approach raises the AUC from 0.81 to 0.96 on optically clear cases, offering real‑time, privacy‑by‑design feedback to filter ungradable photo sets before clinician review.