IMMUNOHISTOCHEMICAL ASSESSMENT OF TUMOR VASCULARITY IN RECURRENT CLARK-II MELANOMAS USING ANTIBODY TO TYPE-IV COLLAGEN

被引:9
作者
GUFFEY, JM
CHANEY, JV
STEVENS, GL
SCHROER, KR
FENSKE, NA
REINTGEN, D
GLASS, LF
机构
[1] UNIV S FLORIDA,JAMES A HALEY VET HOSP,MOFFITT CANC CTR,CUTANEOUS ONCOL PROGRAM,TAMPA,FL
[2] UNIV S FLORIDA,JAMES A HALEY VET HOSP,RES INST,TAMPA,FL
关键词
D O I
10.1111/j.1600-0560.1995.tb01393.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Thin melanomas, measuring 0.76 mm or less, are generally associated with an excellent prognosis. However, a certain subset of these seemingly innocuous lesions have been reported to develop recurrences. Therefore, the predictive values of currently accepted prognostic indicators have been questioned in thin melanomas. Several studies concerning tumor vascularity in melanoma and certain non-melanocytic malignancies suggest that the degree of vascularization correlates with growth rate and biologic aggressiveness. In the present study, we determined the vascularity of a small group of Clark level II melanomas that resulted in recurrence, and compared these results to an equal number of nonrecurrent lesions with similar prognostic indicators. Blood vessels were labeled by immunoperoxidase staining techniques for Type IV collagen, and quantified by image analysis. No statistical difference was found between the two groups when mean blood vessel counts and percent vascular area were measured. The recurrent tumors had a mean PVA of 4.68 compared to 4.34 for the nonrecurrent group (p = 0.677). The mean blood vessel count beneath the recurrent group was 29.6 per 400 x field, and the corresponding value for the nonrecurrent group was 31.8 (p = 0.681). Our data is preliminary within this limited group of tumors, yet it suggests that tumor vascularity is not a distinctive prognostic indicator by which eventual outcome can be predicted in thin Clark level II malignant melanomas.
引用
收藏
页码:122 / 127
页数:6
相关论文
共 57 条
[1]
BAGLEY FH, 1981, CANCER-AM CANCER SOC, V47, P2126, DOI 10.1002/1097-0142(19810501)47:9<2126::AID-CNCR2820470904>3.0.CO
[2]
2-C
[3]
BARNHILL RL, 1993, AM J PATHOL, V143, P99
[4]
BARNHILL RL, 1992, LAB INVEST, V67, P331
[5]
ANGIOGENESIS AND THE SKIN [J].
BARNHILL, RL ;
WOLF, JE .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1987, 16 (06) :1226-1242
[6]
BRESLOW A, 1976, SURG GYNECOL OBSTET, V143, P799
[7]
EVALUATION OF PROGNOSIS IN STAGE-I CUTANEOUS MELANOMA [J].
BRESLOW, A ;
MACHT, SD .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1978, 61 (03) :342-346
[9]
EXPERIENCE OF THIN CUTANEOUS MELANOMAS (LESS-THAN 0.76MM AND LESS-THAN 0.85MM THICK) IN A LARGE PLASTIC-SURGERY UNIT - A 5 TO 17 YEAR FOLLOW-UP [J].
BRIGGS, JC ;
IBRAHIM, NBN ;
HASTINGS, AG ;
GRIFFITHS, RW .
BRITISH JOURNAL OF PLASTIC SURGERY, 1984, 37 (04) :501-506
[10]
THE VASCULARITY OF CUTANEOUS MELANOMA - A QUANTITATIVE HISTOLOGICAL STUDY OF LESIONS 0.85-1.25MM IN THICKNESS [J].
CARNOCHAN, P ;
BRIGGS, JC ;
WESTBURY, G ;
DAVIES, AJS .
BRITISH JOURNAL OF CANCER, 1991, 64 (01) :102-107