Frequency and characteristics of enlarging common melanocytic nevi

被引:111
作者
Kittler, H
Seltenheim, M
Dawid, M
Pehamberger, H
Wolff, K
Binder, M
机构
[1] Univ Vienna, Sch Med, Dept Dermatol, Div Gen Dermatol, A-1090 Vienna, Austria
[2] Ludwig Boltzman Inst Clin & Expt Oncol, Vienna, Austria
关键词
D O I
10.1001/archderm.136.3.316
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: To analyze the frequency and characteristics of enlarging common melanocytic nevi. Design: Cohort study using digital epiluminescence microscopy (ELM) for documentation and follow-up, with a median follow-up interval of 11.4 months. Setting: A dermatology department at a university hospital in Vienna, Austria. Patients: One thousand six hundred twelve melanocytic nevi appearing clinically as common nevi, obtained from 385 patients (mean [+/-SD] age, 34.2 +/- 14.8 y; 55.6% female). Interventions: Follow-up examination and documentation by digital ELM. Main Outcome Measures: Frequency of enlarging nevi according to age and comparison of ELM features observed in enlarging and nonenlarging nevi. Results: Enlargement was found in 5.3% (n = 86) of nevi. The frequency of enlarging nevi was inversely related to age (P<.001), in that enlarging nevi were common in pa -tients younger than 20 years and relatively rare in older age groups. Epiluminescence microscopy revealed a peripheral rim of brown globules in 48.8% (n = 42) of enlarging nevi. In contrast, a peripheral rim of brown, globules was found in only 0.7% (n = 11) of nevi without enlargement (P<.001). Enlarging nevi that were excised in children and adolescents showed no histological signs of atypia. Tn older age groups, 48.1% of excised enlarging nevi that were clinically diagnosed as common nevi showed some histological signs of atypia. None of the excised enlarging lesions was histologically diagnosed as melanoma. Conclusions: The frequency of enlarging common nevi is inversely related to age. In the absence of clinical signs of atypia, enlargement alone does not indicate malignancy. A peripheral rim of brown globules is a characteristic ELM feature of symmetrically enlarging melanocytic nevi.
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页码:316 / 320
页数:5
相关论文
共 18 条
[1]  
BAHMER FA, 1990, HAUTARZT, V41, P513
[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]   A statistical analysis of the characteristics of pigmented skin lesions using epiluminescence microscopy [J].
Delfino, M ;
Fabbrocini, G ;
Argenziano, G ;
Magliocchetti, N ;
Nofroni, I .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 1997, 9 (03) :243-248
[4]   Epiluminescence videomicroscopy: Black dots and brown globules revisited by stripping the stratum corneum [J].
Guillod, JF ;
Skaria, AM ;
Salomon, D ;
Saurat, JH .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 36 (03) :371-377
[5]   NATURAL-HISTORY OF DYSPLASTIC NEVI [J].
HALPERN, AC ;
GUERRY, D ;
ELDER, DE ;
TROCK, B ;
SYNNESTVEDT, M ;
HUMPHREYS, T .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1993, 29 (01) :51-57
[6]   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
[7]   A sensitivity and specificity analysis of the surface microscopy features of invasive melanoma [J].
Menzies, SW ;
Ingvar, C ;
McCarthy, WH .
MELANOMA RESEARCH, 1996, 6 (01) :55-62
[8]   INVIVO EPILUMINESCENCE MICROSCOPY OF PIGMENTED SKIN-LESIONS .1. PATTERN-ANALYSIS OF PIGMENTED SKIN-LESIONS [J].
PEHAMBERGER, H ;
STEINER, A ;
WOLFF, K .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1987, 17 (04) :571-583
[9]  
PuspokSchwarz M, 1997, MELANOMA RES, V7, P307
[10]   Congenital nevomelanocytic nevi: Proportionate area expansion during infancy and early childhood [J].
Rhodes, AR ;
Albert, LS ;
Weinstock, MA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 34 (01) :51-62