How often are diagnostic features missed with less extensive histologic sampling of prostate needle biopsy specimens?

被引:26
作者
Brat, DJ [1 ]
Wills, ML [1 ]
Lecksell, KL [1 ]
Epstein, JI [1 ]
机构
[1] Johns Hopkins Hosp, Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21287 USA
关键词
prostate cancer; histologic sampling; core biopsy; misdiagnosis;
D O I
10.1097/00000478-199903000-00002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The authors determined whether clinically relevant diagnostic information would be lost by examination of < 3 levels per tissue core in prostate needle biopsy specimens. They evaluated 439 consecutive sextant biopsy specimens for the following three histopathologic features: presence of adenocarcinoma involving one core, Gleason pattern 4 in cases of grade 3 + 4 = 7 adenocarcinoma, and perineural invasion (PNI) by carcinoma. For all cases, 3 levels from each involved core were reviewed for the presence or absence of these three features. In 50 cases with adenocarcinoma involving only 1 core, diagnostic carcinoma was present on all 3 levels in 43 cores (86%). Carcinoma was present on only 2 levels in 3 cores (6%), present only on 1 level in 3 cores (6%), and present only on additional cut-downs, not on the original 3 levels in 1 core (2%). Among 32 cases, 51 cores were identified that contained Gleason grade 3 + 4 = 7 adenocarcinoma. In 41 cores (80%), pattern 4 was identified in all 3 levels. In 5 cores (10%), pattern 4 was identified on only 2 levels, and in another 5 cores (10%), pattern 4 was present on only 1 level. Among 36 cases, 69 tissue cores were identified that contained perineural invasion (PNI). In 54 cores (78%), PNI was present on all 3 levels. In 7 cores (10%), PNI was present on only 2 of 3 levels, while in 7 other cores (10%), PNI was present on only 1 of 3 levels. In 1 core (1.5%), PM was noted only on additional cut-downs, not on the original 3 levels. We estimated that reducing the number of levels to 1 per core could result in the misdiagnosis of PNI, grading, or carcinoma in similar to 8-11% of cores with these features and could have changed the case diagnosis in 9 of 439 cases. If only 2 levels were reviewed, we predict misdiagnosis in 5% to 6% of cores with these features and a change in the case diagnosis in 5 of 439 cases. Misdiagnosis of clinically relevant features on prostate biopsy specimens can be minimized with histologic review of 3 levels per tissue core.
引用
收藏
页码:257 / 262
页数:6
相关论文
共 14 条
[1]  
AMIN MB, 1998, PATHOL CASE REV, V3, P223
[2]   Prediction of capsular perforation and seminal vesicle invasion in prostate cancer [J].
Bostwick, DG ;
Qian, JQ ;
Bergstralh, E ;
Dundore, P ;
Dugan, J ;
Myers, RP ;
Oesterling, JE .
JOURNAL OF UROLOGY, 1996, 155 (04) :1361-1367
[3]   SAMPLING OF RADICAL PROSTATECTOMY SPECIMENS - HOW MUCH IS ADEQUATE [J].
COHEN, MB ;
SOLOWAY, MS ;
MURPHY, WM .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1994, 101 (03) :250-252
[4]   Prediction of progression following radical prostatectomy - A multivariate analysis of 721 men with long-term follow-up [J].
Epstein, JI ;
Partin, AW ;
Sauvageot, J ;
Walsh, PC .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (03) :286-292
[5]  
HALL GS, 1992, AM J SURG PATHOL, V16, P184
[6]  
HOLMES GF, 1999, IN PRESS UROLOGY
[7]   ADENOCARCINOMA OF THE PROSTATE .1. TISSUE SAMPLING CONSIDERATIONS [J].
HUMPHREY, PA ;
WALTHER, PJ .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1993, 99 (06) :746-759
[8]  
MCNEAL JE, 1990, CANCER, V66, P1225, DOI 10.1002/1097-0142(19900915)66:6<1225::AID-CNCR2820660624>3.0.CO
[9]  
2-X
[10]   Combination of prostate-specific antigen, clinical stage, and gleason score to predict pathological stage of localized prostate cancer - A multi-institutional update [J].
Partin, AW ;
Kattan, MW ;
Subong, ENP ;
Walsh, PC ;
Wojno, KJ ;
Oesterling, JE ;
Scardino, PT ;
Pearson, JD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (18) :1445-1451