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1.
Skin Res Technol ; 18(2): 133-42, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-21507072

RESUMO

BACKGROUND/PURPOSE: Border (B) description of melanoma and other pigmented skin lesions is one of the most important tasks for the clinical diagnosis of dermoscopy images using the ABCD rule. For an accurate description of the border, there must be an effective skin tumor area extraction (STAE) method. However, this task is complicated due to uneven illumination, artifacts present in the lesions and smooth areas or fuzzy borders of the desired regions. METHODS: In this paper, a novel STAE algorithm based on improved dynamic programming (IDP) is presented. The STAE technique consists of the following four steps: color space transform, pre-processing, rough tumor area detection and refinement of the segmented area. The procedure is performed in the CIE L(*) a(*) b(*) color space, which is approximately uniform and is therefore related to dermatologist's perception. After pre-processing the skin lesions to reduce artifacts, the DP algorithm is improved by introducing a local cost function, which is based on color and texture weights. RESULTS: The STAE method is tested on a total of 100 dermoscopic images. In order to compare the performance of STAE with other state-of-the-art algorithms, various statistical measures based on dermatologist-drawn borders are utilized as a ground truth. The proposed method outperforms the others with a sensitivity of 96.64%, a specificity of 98.14% and an error probability of 5.23%. CONCLUSION: The results demonstrate that this STAE method by IDP is an effective solution when compared with other state-of-the-art segmentation techniques. The proposed method can accurately extract tumor borders in dermoscopy images.


Assuntos
Dermoscopia/métodos , Processamento de Imagem Assistida por Computador/métodos , Melanoma/patologia , Neoplasias/patologia , Neoplasias Cutâneas/patologia , Algoritmos , Artefatos , Bases de Dados Factuais , Dermoscopia/instrumentação , Diagnóstico Diferencial , Humanos , Processamento de Imagem Assistida por Computador/instrumentação , Modelos Biológicos , Sensibilidade e Especificidade , Design de Software
2.
Skin Res Technol ; 17(1): 91-100, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21226876

RESUMO

BACKGROUND/PURPOSE: Automated border detection is an important and challenging task in the computerized analysis of dermoscopy images. However, dermoscopic images often contain artifacts such as illumination, dermoscopic gel, and outline (hair, skin lines, ruler markings, and blood vessels). As a result, there is a need for robust methods to remove artifacts and detect lesion borders in dermoscopy images. METHODS: This automated method consists of three main steps: (1) preprocessing, (2) edge candidate point detection, and (3) tumor outline delineation. First, algorithms to reduce artifacts were used. Second, a least-squares method (LSM) was performed to acquire edge points. Third, dynamic programming (DP) technique was used to find the optimal boundary of the lesion. Statistical measures based on dermatologist-drawn borders were utilized as ground-truth to evaluate the performance of the proposed method. RESULTS: The method is tested on a total of 240 dermoscopic images: 30 benign melanocytic, 50 malignant melanomas, 50 basal cell carcinomas, 20 Merkel cell carcinomas, 60 seborrheic keratosis, and 30 atypical naevi. We obtained mean border detection error of 8.6%, 5.04%, 9.0%, 7.02%, 2.01%, and 3.24%, respectively. CONCLUSIONS: The results demonstrate that border detection combined with artifact removal increases sensitivity and specificity for segmentation of lesions in dermoscopy images.


Assuntos
Dermoscopia/métodos , Processamento de Imagem Assistida por Computador/métodos , Melanoma/patologia , Neoplasias Cutâneas/patologia , Software , Artefatos , Carcinoma Basocelular/patologia , Bases de Dados Factuais , Dermoscopia/instrumentação , Cabelo , Humanos , Processamento de Imagem Assistida por Computador/instrumentação , Ceratose Seborreica/patologia , Lentigo/patologia , Modelos Biológicos , Neoplasias/patologia , Nevo/patologia , Sensibilidade e Especificidade
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