ASSOCIATED FACTORS IN THE PREVALENCE OF MORE THAN 50 COMMON MELANOCYTIC NEVI, ATYPICAL MELANOCYTIC NEVI, AND ACTINIC LENTIGINES - MULTICENTER CASE-CONTROL STUDY OF THE CENTRAL MALIGNANT-MELANOMA REGISTRY OF THE GERMAN-DERMATOLOGICAL-SOCIETY
C. Garbe et al., ASSOCIATED FACTORS IN THE PREVALENCE OF MORE THAN 50 COMMON MELANOCYTIC NEVI, ATYPICAL MELANOCYTIC NEVI, AND ACTINIC LENTIGINES - MULTICENTER CASE-CONTROL STUDY OF THE CENTRAL MALIGNANT-MELANOMA REGISTRY OF THE GERMAN-DERMATOLOGICAL-SOCIETY, Journal of investigative dermatology, 102(5), 1994, pp. 700-705
Several case-control studies identified common and atypical melanocyti
c nevi as major risk indicators for the development of cutaneous melan
oma. The present investigation was planned to detect factors associate
d with the prevalence of these melanoma risk markers. Whole-body exami
nation findings and interview data of 513 melanoma patients and 498 ag
e- and sex-matched control subjects were analyzed. Existence of more t
han 50 common melanocytic nevi and the presence of atypical melanocyti
c nevi were significantly related to age and gender, with significantl
y elevated relative risk for their prevalence before the age of 60 and
in males. Additionally, sunburns before the age of 20 were significan
tly associated with both more than 50 common melanocytic nevi (relativ
e risk = 1.7) and the presence of atypical melanocytic nevi (relative
risk = 1.5). Actinic lentigines were found more frequently with increa
sing age, and the presence of actinic lentigines was significantly rel
ated to a tendency of freckling in adolescence (relative risk = 2.0) a
nd to two or more sunburns after the age of 20 (relative risk = 1.6).
In conclusion, sunburns before the age of 20 contribute to the develop
ment of multiple melanocytic nevi and atypical melanocytic nevi. In ad
ulthood, this type of sun exposure is associated with the development
of actinic lentigines. The relative risk of developing cutaneous melan
oma increases in association with the development of these benign mela
nocytic lesions.