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Clinically recognized dysplastic nevi - A central risk factor for cutaneous melanoma
Author(s): Tucker MA, Halpern A, Holly EA, Hartge P, Elder DE, Sagebiel RW, Guerry D, Clark WH
Source: JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION    Volume: 277    Issue: 18    Pages: 1439-1444    Published: MAY 14 1997  
Times Cited: 193     References: 44     
Abstract: Objective.-To investigate the relationship of number and type of nevi to the development of melanoma.

Design.-Case-control study.

Setting.-Outpatient clinics in referral hospitals.

Patients.-Cases were 716 consecutive patients with newly diagnosed melanoma identified at 2 melanoma centers between January 1, 1991, and December 31, 1992. Stratified random sampling of patients from outpatient clinics was used to identify 1014 participating controls of the same age, sex, race, and geographic distribution as the melanoma cases. All study subjects underwent an interview, a complete skin examination, photography of the most atypical nevi, and, if the patient was willing, a biopsy of the most atypical nevus.

Main Outcome Measures.-Number and type of nevi on the entire body were systematically reported. All diagnoses of clinically dysplastic nevi were confirmed by expert examiners.

Results.-Risk for melanoma was strongly related to number of small nevi, large nondysplastic nevi, and clinically dysplastic nevi. In the absence of dysplastic nevi, increased numbers of small nevi were associated with an approximately 2-fold risk, and increased numbers of both small and large nondysplastic nevi were associated with a 4-fold risk. One clinically dysplastic nevus was associated with a 2-fold risk (95% confidence interval, 1.4-3.6), while 10 or more conferred a 12-fold increased risk (95% confidence interval, 4.4-31). Congenital nevi were not associated with increased risk of melanoma.

Conclusions.-Although nondysplastic nevi confer a small risk, clinically dysplastic nevi confer substantial risk for melanoma. On the basis of nevus number and type, clinicians can identify a population at high risk of this epidemic cancer for screening and intervention.

Document Type: Article
Language: English
Reprint Address: Tucker, MA (reprint author), NCI, GENET EPIDEMIOL BRANCH, NIH, EXECUT PLAXA N, SUITE 439, 6130 EXECUT BLVD, BETHESDA, MD 20892 USA
Addresses:
1. NCI, ENVIRONM EPIDEMIOL BRANCH, NIH, BETHESDA, MD 20892 USA
2. UNIV PENN, SCH MED, PIGMENTED LES STUDY GRP, PHILADELPHIA, PA 19104 USA
3. UNIV CALIF SAN FRANCISCO, DEPT EPIDEMIOL, SAN FRANCISCO, CA 94143 USA
4. UNIV CALIF SAN FRANCISCO, MELANOMA CLIN, SAN FRANCISCO, CA 94143 USA
Publisher: AMER MEDICAL ASSOC, 515 N STATE ST, CHICAGO, IL 60610
Subject Category: Medicine, General & Internal
IDS Number: WX852
ISSN: 0098-7484
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