MULTIPLE MELANOMA AND ATYPICAL MELANOCYTIC NAEVI EVIDENCE OF AN ACTIVATED AND EXPANDED MELANOCYTIC SYSTEM

被引:54
作者
MACKIE, RM
机构
关键词
D O I
10.1111/j.1365-2133.1982.tb00519.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:621 / 629
页数:9
相关论文
共 19 条
[1]   PRIMARY CHOROIDAL AND CUTANEOUS MELANOMAS OCCURRING IN A PATIENT WITH THE B-K MOLE SYNDROME PHENOTYPE [J].
BELLET, RE ;
SHIELDS, JA ;
SOLL, DB ;
BERNARDINO, EA .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1980, 89 (04) :567-570
[2]  
BRAUNFALCO O, 1979, FORTSCHR MED, V97, P1489
[3]  
BRAUNINGER BK, 1981, DERMATOLOGICA, V162, P191
[4]   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
[5]   HISTOLOGY AND PROGNOSIS IN MALIGNANT MELANOMA [J].
COCHRAN, AJ .
JOURNAL OF PATHOLOGY, 1969, 97 (03) :459-&
[6]  
ELDER DE, 1980, CANCER, V46, P1787, DOI 10.1002/1097-0142(19801015)46:8<1787::AID-CNCR2820460816>3.0.CO
[7]  
2-S
[8]  
FRICHOT BC, 1977, LANCET, V1, P864
[9]  
GREENE MH, 1980, 16TH P M AM SOC CLIN, P323
[10]  
HUNDEIKER M, 1980, HAUTARZT, V31, P42