Early melanoma detection: Nonuniform dermoscopic features and growth

被引:51
作者
Lucas, CR [1 ]
Sanders, LL [1 ]
Murray, JC [1 ]
Myers, SA [1 ]
Hall, RP [1 ]
Grichnik, JM [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Div Dermatol, Durham, NC 27710 USA
关键词
D O I
10.1067/mjd.2003.283
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Dermoscopy alone is not sufficient to detect all early melanomas. Total body photos reveal growth of melanomas but also reveal growth of melanocytic nevi. Objective: We set Out to determine whether a simplified algorithm on the basis of nonuniform dermoscopic features combined with growth noted from baseline total body photos targeted the early melanocytic neoplasms most likely to be malignant. Methods: Lesions removed during follow-up of patients with total body photographs were reviewed and 169 melanocytic lesions were identified for which both gross clinical and dermoscopic photos were available. The images were evaluated separately by 3 academic dermatologists, without knowledge of the given pathologic diagnosis, for uniformity (consistent gradient of features from center to edge) and change (specifically, that which could indicate melanoma growth in normal skin or within a nevus). Results. Using a minimum of 2 out of 3 agreement for uniformity and change, 12 of 16 melanomas (including all 5 superficially invasive tumors) were graded as nonuniform and changed. The 4 melanomas not included in this category were in situ. The predicted odds of melanoma for lesions scored as both nonuniform and changed was 4.06 (P > .0195), If 3 out of 3 agreement was used, the odds ratio increased to 6 (P > .0010). Conclusion: An algorithm on the basis of dermoscopic nonuniformity and change suggestive of growth as determined by total body photography segregates melanocytic neoplasms most likely to be malignant.
引用
收藏
页码:663 / 671
页数:9
相关论文
共 22 条
[1]   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
[2]   THE EPIDEMIOLOGY OF ACQUIRED MELANOCYTIC NEVI - A BRIEF REVIEW [J].
GALLAGHER, RP ;
MCLEAN, DI .
DERMATOLOGIC CLINICS, 1995, 13 (03) :595-603
[3]  
GRICHNIK J, 1998, MELANOMA LETT, V16, P3
[4]   The 'ugly duckling' sign: Identification of the common characteristics at nevi in an individual as a basis for melanoma screening [J].
Grob, JJ ;
Bonerandi, JJ .
ARCHIVES OF DERMATOLOGY, 1998, 134 (01) :103-104
[5]  
HALPERN AC, 1993, J INVEST DERMATOL, V100, P346
[6]   A high incidence of melanoma found in patients with multiple dysplastic naevi by photographic surveillance [J].
Kelly, JW ;
Yeatman, JM ;
Regalia, G ;
Mason, G ;
Henham, AP .
MEDICAL JOURNAL OF AUSTRALIA, 1997, 167 (04) :191-194
[7]   CLINICAL-DIAGNOSIS OF PIGMENTED LESIONS USING DIGITAL EPILUMINESCENCE MICROSCOPY - GRADING PROTOCOL AND ATLAS [J].
KENET, RO ;
KANG, S ;
KENET, BJ ;
FITZPATRICK, TB ;
SOBER, AJ ;
BARNHILL, RL .
ARCHIVES OF DERMATOLOGY, 1993, 129 (02) :157-174
[8]   Follow-up of melanocytic skin lesions with digital epiluminescence microscopy: Patterns of modifications observed in early melanoma, atypical nevi, and common nevi [J].
Kittler, H ;
Pehamberger, H ;
Wolff, K ;
Binder, M .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 43 (03) :467-476
[9]   ACCELERATED DETECTION WITH PROSPECTIVE SURVEILLANCE FOR CUTANEOUS MALIGNANT-MELANOMA IN HIGH-RISK GROUPS [J].
MACKIE, RM ;
MCHENRY, P ;
HOLE, D .
LANCET, 1993, 341 (8861) :1618-1620
[10]   RISK OF CUTANEOUS MALIGNANT-MELANOMA IN PATIENTS WITH CLASSIC ATYPICAL-MOLE SYNDROME - A CASE-CONTROL STUDY [J].
MARGHOOB, AA ;
KOPF, AW ;
RIGEL, DS ;
BART, RS ;
FRIEDMAN, RJ ;
YADAV, S ;
ABADIR, M ;
SANFILIPPO, L ;
SILVERMAN, MK ;
VOSSAERT, KA .
ARCHIVES OF DERMATOLOGY, 1994, 130 (08) :993-998