Assessment of the optimal interval for and sensitivity of short-term sequential digital dermoscopy monitoring for the diagnosis of melanoma

被引:107
作者
Altamura, Davide [2 ]
Avramidis, Michelle [1 ]
Menzies, Scott W. [1 ,3 ]
机构
[1] Royal Prince Alfred Hosp, Sydney Canc Ctr, Sydney Melanoma Diagnost Ctr, Camperdown, NSW 2050, Australia
[2] Univ Aquila, Dept Dermatol, I-67100 Laquila, Italy
[3] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia
关键词
D O I
10.1001/archderm.144.4.502
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: To determine whether 6 weeks could replace 3 months for short-term sequential digital dermoscopy imaging (ST-SDDI) of suspicious melanocytic lesions and determine the proportion of melanomas missed. Design: Consecutive lesions (n=2602) undergoing ST-SDDI monitored from 1859 patients were included. Half of the patients underwent 6-week monitoring followed by 3-month monitoring (range, 2.5-4.5 months) if changes were not seen. The remainder underwent 3-month monitoring only. Any change during this time led to excision. Lesions unchanged were then followed up over time. Setting: A teritary referrel instituion Main Outcome Measures: The proportion of changed melanomas (sensitivity) and odds ratios (ORs) for melanoma of changed lesions. Results: Eighty-one melanomas were detected using ST-SDDI (Breslow thickness: median, in situ; maximum, 0.8 mm). Of 39 melanomas detected using ST-SDDI in the 6-week monitored lesions, 27 (69%) were detected at 6 weeks and 12 (31%) at 3 months. The OR for melanoma for a lesion changing at 6 weeks was 19 (95% confidence interval [CI], 10-35), and the overall OR for melanoma for a lesion changing during the short-term monitoring period (6 weeks to 4.5 months) was 47 (95% CI, 23-94). For lesions remaining unchanged at 3 months, 99.2% (1118 of 1127 lesions) were shown to be benign as defined by an unremarkable further follow-up. Seventy-five percent (15 of 20) of the lentigo maligna melanomas, 93% (40 of 43) of other in situ melanomas, and 96% (26 of 27) of the invasive melanomas were detected using ST-SDDI. Conclusion: Three months remains the standard interval for ST-SDDI, where the sensitivity for the diagnosis of melanoma for changed (non-lentigo maligna) lesions is high but not 100%.
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页码:502 / 506
页数:5
相关论文
共 12 条
[1]   Surveillance of patients at high risk for cutaneous malignant melanoma using digital dermoscopy [J].
Bauer, J ;
Blum, A ;
Strohhäcker, U ;
Garbe, C .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (01) :87-92
[2]   Two types of pattern modification detected on the follow-up of benign melanocytic skin lesions by digitized epiluminescence microscopy [J].
Braun, RP ;
Lemonnier, E ;
Guillod, J ;
Skaria, A ;
Salomon, D ;
Saurat, JH .
MELANOMA RESEARCH, 1998, 8 (05) :431-437
[3]   Results from an observational trial: Digital epiluminescence Microscopy follow-up of atypical nevi increases the sensitivity and the chance of success of conventional dermoscopy in detecting melanoma [J].
Haenssle, Holger A. ;
Krueger, Ullrich ;
Vente, Claudia ;
Thoms, Kai-Martin ;
Bertsch, Hans P. ;
Zutt, Markus ;
Rosenberger, Albert ;
Neumann, Christine ;
Emmert, Steffen .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (05) :980-985
[4]   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
[5]   Identification of clinically featureless incipient melanoma using sequential dermoscopy imaging [J].
Kittler, Harald ;
Guitera, Pascale ;
Riedl, Elisabeth ;
Avramidis, Michelle ;
Teban, Ligia ;
Fiebiger, Manfred ;
Weger, Rickard A. ;
Dawid, Markus ;
Menzies, Scott .
ARCHIVES OF DERMATOLOGY, 2006, 142 (09) :1113-1119
[6]   Follow-up of melanocytic skin lesions with digital total-body photography and digital dermoscopy: A two-step method [J].
Malvehy, J ;
Puig, S .
CLINICS IN DERMATOLOGY, 2002, 20 (03) :297-304
[7]   Frequency and morphologic characteristics of invasive melanomas lacking specific Surface microscopic features [J].
Menzies, SW ;
Ingvar, C ;
Crotty, KA ;
McCarthy, WH .
ARCHIVES OF DERMATOLOGY, 1996, 132 (10) :1178-1182
[8]  
Menzies SW, 2001, ARCH DERMATOL, V137, P1583
[9]   Digital epiluminescence microscopy monitoring of high-risk patients [J].
Robinson, JK ;
Nickoloff, BJ .
ARCHIVES OF DERMATOLOGY, 2004, 140 (01) :49-56
[10]   Long-term dermoscopic follow-up of melanocytic naevi: clinical outcome and patient compliance [J].
Schiffner, R ;
Schiffner-Rohe, J ;
Landthaler, M ;
Stolz, W .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 149 (01) :79-86