Colour histogram analysis for melanoma discrimination in clinical images

被引:37
作者
Faziloglu, Y
Stanley, RJ
Moss, RH
Van Stoecker, W
McLean, RP
机构
[1] Univ Missouri, Dept Elect & Comp Engn, Rolla, MO 65409 USA
[2] Stoecker & Associates, Rolla, MO 65401 USA
关键词
image processing; dermatology; colour; malignant melanoma; histogram;
D O I
10.1034/j.1600-0846.2003.00030.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Malignant melanoma, the most deadly form of skin cancer, has a good prognosis if treated in the curable early stages. Colour provides critical discriminating information for the diagnosis of malignant melanoma. Methods: This research introduces a three-dimensional relative colour histogram analysis technique to identify colours characteristic of melanomas and then applies these 'melanoma colours' to differentiate benign skin lesions from melanomas. The relative colour of a skin lesion is determined based on subtracting a representative colour of the surrounding skin from each lesion pixel. A colour mapping for 'melanoma colours' is determined using a training set of images. A percent melanoma colour feature, defined as the percentage of the lesion pixels that are melanoma colours, is used for discriminating melanomas from benign lesions. The technique is evaluated using a clinical image data set of 129 malignant melanomas and 129 benign lesions consisting of 40 seborrheic keratoses and 89 nevocellular nevi. Results: Using the percent melanoma colour feature for discrimination, experimental results yield correct melanoma and benign lesion discrimination rates of 84.3 and 83.0%, respectively. Conclusions: The results presented in this work suggest that lesion colour in clinical images is strongly related to the presence of melanoma in that lesion. However, colour information should be combined with other information in order to further reduce the false negative and false positive rates.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 27 条
[1]  
Aitken JF, 1996, CANCER, V78, P252, DOI 10.1002/(SICI)1097-0142(19960715)78:2<252::AID-CNCR10>3.0.CO
[2]  
2-V
[3]  
Andreassi L., 1995, CHRONICA DERMATOL, V1, P11
[4]   HOW WELL DO PHYSICIANS RECOGNIZE MELANOMA AND OTHER PROBLEM LESIONS [J].
CASSILETH, BR ;
CLARK, WH ;
LUSK, EJ ;
FREDERICK, BE ;
THOMPSON, CJ ;
WALSH, WP .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1986, 14 (04) :555-560
[5]   SHAPE-ANALYSIS FOR CLASSIFICATION OF MALIGNANT-MELANOMA [J].
CLARIDGE, E ;
HALL, PN ;
KEEFE, M ;
ALLEN, JP .
JOURNAL OF BIOMEDICAL ENGINEERING, 1992, 14 (03) :229-234
[6]  
DHAWAN AP, 1988, ANAL QUANT CYTOL, V10, P405
[7]   ART-based image analysis for pigmented lesions of the skin [J].
Donohoe, GW ;
Nemeth, S ;
Soliz, P .
11TH IEEE SYMPOSIUM ON COMPUTER-BASED MEDICAL SYSTEMS, PROCEEDINGS, 1998, :293-298
[8]   NEURAL-NETWORK DIAGNOSIS OF MALIGNANT-MELANOMA FROM COLOR IMAGES [J].
ERCAL, F ;
CHAWLA, A ;
STOECKER, WV ;
LEE, HC ;
MOSS, RH .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1994, 41 (09) :837-845
[9]   EARLY DETECTION OF MALIGNANT-MELANOMA - THE ROLE OF PHYSICIAN EXAMINATION AND SELF-EXAMINATION OF THE SKIN [J].
FRIEDMAN, RJ ;
RIGEL, DS ;
KOPF, AW .
CA-A CANCER JOURNAL FOR CLINICIANS, 1985, 35 (03) :130-151
[10]   Automated melanoma recognition [J].
Ganster, H ;
Pinz, A ;
Röhrer, R ;
Wildling, E ;
Binder, M ;
Kittler, H .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 2001, 20 (03) :233-239