Learning to Detect Blue-White Structures in Dermoscopy Images With Weak Supervision.

We propose a novel approach to identify one of the most significant dermoscopic criteria in the diagnosis of cutaneous Melanoma: the blue-white structure (BWS). In this paper, we achieve this goal in a multiple instance learning (MIL) framework using only image-level labels indicating whether the feature is present or not. To this aim, each image is represented as a bag of (nonoverlapping) regions, where each region may or may not be identified as an instance of BWS. A probabilistic graphical model is trained (in MIL fashion) to predict the bag (image) labels. As output, we predict the classification label for the image (i.e., the presence or absence of BWS in each image) and we also localize the feature in the image. Experiments are conducted on a challenging dataset with results outperforming state-of-the-art techniques, with BWS detection besting competing methods in terms of performance. This study provides an improvement on the scope of modeling for computerized image analysis of skin lesions. In particular, it propounds a framework for identification of dermoscopic local features from weakly labeled data.

Incorporating Colour Information for Computer-Aided Diagnosis of Melanoma from Dermoscopy Images: A Retrospective Survey and Critical Analysis.

Cutaneous melanoma is the most life-threatening form of skin cancer. Although advanced melanoma is often considered as incurable, if detected and excised early, the prognosis is promising. Today, clinicians use computer vision in an increasing number of applications to aid early detection of melanoma through dermatological image analysis (dermoscopy images, in particular). Colour assessment is essential for the clinical diagnosis of skin cancers. Due to this diagnostic importance, many studies have either focused on or employed colour features as a constituent part of their skin lesion analysis systems. These studies range from using low-level colour features, such as simple statistical measures of colours occurring in the lesion, to availing themselves of high-level semantic features such as the presence of blue-white veil, globules, or colour variegation in the lesion. This paper provides a retrospective survey and critical analysis of contributions in this research direction.

A probabilistic approach to quantification of melanin and hemoglobin content in dermoscopy images.

We describe a technique that employs the stochastic Latent Topic Models framework to allow quantification of melanin and hemoglobin content in dermoscopy images. Such information bears useful implications for analysis of skin hyperpigmentation, and for classification of skin diseases. The proposed method outperforms existing approaches while allowing for more stringent and probabilistic modeling than previously.

Automatic detection of blue-white veil by discrete colour matching in dermoscopy images.

Skin lesions are often comprised of various colours. The presence of multiple colours with an irregular distribution can signal malignancy. Among common colours under dermoscopy, blue-grey (blue-white veil) is a strong indicator of malignant melanoma. Since it is not always easy to visually identify and recognize this feature, a computerised automatic colour analysis method can provide the clinician with an objective second opinion. In this paper, we put forward an innovative method, through colour analysis and computer vision techniques, to automatically detect and segment blue-white veil areas in dermoscopy images. The proposed method is an attempt to mimic the human perception of lesion colours, and improves and outperforms the state-of-the-art as shown in our experiments.

Intrinsic melanin and hemoglobin colour components for skin lesion malignancy detection.

In this paper we propose a new log-chromaticity 2-D colour space, an extension of previous approaches, which succeeds in removing confounding factors from dermoscopic images: (i) the effects of the particular camera characteristics for the camera system used in forming RGB images; (ii) the colour of the light used in the dermoscope; (iii) shading induced by imaging non-flat skin surfaces; (iv) and light intensity, removing the effect of light-intensity falloff toward the edges of the dermoscopic image. In the context of a blind source separation of the underlying colour, we arrive at intrinsic melanin and hemoglobin images, whose properties are then used in supervised learning to achieve excellent malignant vs. benign skin lesion classification. In addition, we propose using the geometric-mean of colour for skin lesion segmentation based on simple grey-level thresholding, with results outperforming the state of the art.