MALIGNANT-MELANOMA IN CHILDREN

被引:17
作者
CHUN, K [1 ]
VAZQUEZ, M [1 ]
SANCHEZ, JL [1 ]
机构
[1] UNIV PUERTO RICO,SCH MED,DEPT DERMATOL,POB 365067,SAN JUAN,PR 00936
关键词
D O I
10.1111/j.1365-4362.1993.tb00962.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background. While significant risk factors for malignant melanoma may initially develop or are first seen in childhood, the actual occurrence of this neoplasm in prepubertal children is uncommon. Methods. A retrospective study of malignant melanoma in Puerto Ricans up to 16 years of age occurring from 1973 to 1990 was carried out by identifying those cases in the Puerto Rico Cancer Registry. Results. A total of seven cases were found consisting of three boys and four girls with ages ranging from 22 months to 16 years and comprising 0.94% of the total melanomas. In three of the seven cases, there was a history of a previously existent small congenital melanocytic nevus on the area. Three cases were Clark's level I, two level II, and in two cases with proved metastatic disease, Clark's level of invasion were not reported. Those cases with Clark's level I and II had a 100% 5-year survival. Conclusions. Although rare, malignant melanoma in children can be as aggressive as in adults. Among the known factors predisposing to malignant melanoma, three out of seven cases developed within a small congenital nevus, two of which occurred during the first decade of life. Due to the rarity of this event in our population, it appears unreasonable to excise all small congenital nevi during the first decade of life. Even for those who advocate excision of all small congenital nevi, the evidence at present suggests that such small nevi very rarely undergo malignant change before puberty and therefore a policy of observation in childhood and offering excision around the time of puberty is perfectly logical.
引用
收藏
页码:41 / 43
页数:3
相关论文
共 22 条
[1]  
BADER JL, 1985, AM J PEDIAT HEMATOL, V7, P341
[2]   MALIGNANT-MELANOMA IN CHILDREN AND YOUNG-ADULTS - EFFECT OF DIAGNOSTIC CRITERIA ON STAGING AND END RESULTS [J].
BODDIE, AW ;
SMITH, JL ;
MCBRIDE, CM .
SOUTHERN MEDICAL JOURNAL, 1978, 71 (09) :1074-1078
[3]   ORIGIN OF FAMILIAL MALIGNANT MELANOMAS FROM HERITABLE MELANOCYTIC LESIONS - B-K MOLE SYNDROME [J].
CLARK, WH ;
REIMER, RR ;
GREENE, M ;
AINSWORTH, AM ;
MASTRANGELO, MJ .
ARCHIVES OF DERMATOLOGY, 1978, 114 (05) :732-738
[4]   CONGENITAL NEVI LESS-THAN-OR-EQUAL-TO 10 CM AS PRECURSORS TO MELANOMA - 52 CASES, A REVIEW, AND A NEW CONCEPTION [J].
ILLIG, L ;
WEIDNER, F ;
HUNDEIKER, M ;
GARTMANN, H ;
BIESS, B ;
LEYH, F ;
PAUL, E .
ARCHIVES OF DERMATOLOGY, 1985, 121 (10) :1274-1281
[5]   CONGENITAL NEVOCYTIC NEVI AND MALIGNANT MELANOMAS [J].
KOPF, AW ;
BART, RS ;
HENNESSEY, P .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1979, 1 (02) :123-130
[6]  
KOPT AW, 1982, J DERMATOL SURG ONC, V8, P760
[7]   XERODERMA-PIGMENTOSUM - CUTANEOUS, OCULAR, AND NEUROLOGIC ABNORMALITIES IN 830 PUBLISHED CASES [J].
KRAEMER, KH ;
LEE, MM ;
SCOTTO, J .
ARCHIVES OF DERMATOLOGY, 1987, 123 (02) :241-250
[8]  
Lerman R I, 1970, Cancer, V25, P436, DOI 10.1002/1097-0142(197002)25:2<436::AID-CNCR2820250223>3.0.CO
[9]  
2-I
[10]  
MELNIK MK, 1986, AM SURGEON, V52, P142