VIN 3: a clinicopathologic review

被引:46
作者
McNally, OM
Mulvany, NJ
Pagano, R
Quinn, MA
Rome, RM
机构
[1] Aberdeen Royal Infirm, Dept Gynecol Oncol, Foresterhill AB25 2ZN, Scotland
[2] Gippsland Pathol Serv, Gippsland, Australia
[3] Royal Hosp Women, Dept Gynecol Oncol, Melbourne, Vic, Australia
关键词
VIN; 3; margin status; recurrence;
D O I
10.1046/j.1525-1438.2002.01140.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A retrospective review of the management of vulvar intraepithelial neoplasia 3 (VIN 3) over a 16-year period from 1981 to 1997 was conducted. Complete information was available for analysis on 101 patients. The mean age was 53.9 years (range 14-102 years). The mean duration of follow-up was 36 months (range 2-184 months). Fifty-eight percent of patients presented with pruritus. The disease was multifocal in 51% and unifocal in 49% of cases and the left labium majus was the most frequently affected site (27%). Co-existent or previous genital disease was identified in 39% of patients and 8% had a history of invasive gynecological cancer. Histologic evidence of human papillomavirus (HPV) infection was found in 31% of patients. Wide local excision was the most frequently used treatment modality (78%). Thirty-eight percent of patients required at least one further treatment for recurrent disease. Smoking, multifocality, HPV effect, and positive surgical margins were not found to be significant predictors of recurrence. There were three (3%) cases of progression to invasive squamous cell carcinoma of the vulva, one at 6, 7, and 7 years after initial treatment.
引用
收藏
页码:490 / 495
页数:6
相关论文
共 36 条
[1]  
Agarossi A, 1996, J REPROD MED, V41, P665
[2]  
ANDERSON M, 1992, TEXT ATLAS INTEGRATE, P179
[3]   Vulvar intraepithelial neoplasia and carcinoma [J].
Campion, MJ ;
Hacker, NF .
SEMINARS IN CUTANEOUS MEDICINE AND SURGERY, 1998, 17 (03) :205-212
[4]  
CHAFE W, 1988, COLP GYNECOL LAS SUR, V4, P125
[5]  
Edwards CL, 1996, OBSTET GYN CLIN N AM, V23, P295
[6]   Genetic changes during the multistage pathogenesis of human papillomavirus positive and negative vulvar carcinomas [J].
Flowers, LC ;
Wistuba, II ;
Scurry, J ;
Muller, CY ;
Ashfaq, R ;
Miller, DS ;
Minna, JD ;
Gazdar, AF .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 1999, 6 (04) :213-221
[7]   MANAGEMENT OF CARCINOMA INSITU OF VULVA [J].
FORNEY, JP ;
MORROW, CP ;
TOWNSEND, DE ;
DISAIA, PJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1977, 127 (08) :801-806
[8]  
Friedrich R., 1992, Gynaekologisch-Geburtshilfliche Rundschau, V32, P92
[9]   SURGICAL-PATHOLOGICAL VARIABLES PREDICTIVE OF LOCAL RECURRENCE IN SQUAMOUS-CELL CARCINOMA OF THE VULVA [J].
HEAPS, JM ;
FU, YS ;
MONTZ, FJ ;
HACKER, NF ;
BEREK, JS .
GYNECOLOGIC ONCOLOGY, 1990, 38 (03) :309-314
[10]   Vulvar intraepithelial neoplasia: Long term follow up of treated and untreated women [J].
Herod, JJO ;
Shafi, MI ;
Rollason, TP ;
Jordan, JA ;
Luesley, DM .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1996, 103 (05) :446-452