TY - JOUR
T1 - Relationship of severe dysplasia to Stage B adenocarcinoma of the prostate
AU - Quinn, Brian D.
AU - Cho, Kathleen R.
AU - Epstein, Jonathan I.
PY - 1990/5/15
Y1 - 1990/5/15
N2 - Severe dysplasia was studied in totally embedded radical prostatectomy specimens from 40 Stage B, intermediate‐grade prostate cancers. All 40 cases had severe dysplasia which varied in amount (extensive in 35% of cases; intermediate in 55%; minimal in 10%). Severe dysplasia was predominantly concentrated in peripheral and posterior regions of the gland. Those cases with extensive severe dysplasia had more multifocal small cancers (14.6/case) compared with cases with intermediate (7.5/case) or minimal severe dysplasia (5.5/case). Most dominant tumor nodules had some intermingled severe dysplasia, and in 30% of the dominant tumor nodules, intermingled severe dysplasia occupied between 10% and 25% of the tumor nodule. Severe dysplasia was located next to the dominant tumor nodule in all cases. Nineteen percent of dominant tumor nodules had extensive adjacent severe dysplasia ranging from 5 to 14 mm in maximum diameter, showing that the potential exists for needle biopsy of prostate cancers to obtain only severe dysplasia. These data show a close relationship between severe dysplasia and Stage B cancers. In contrast, centrally located low‐grade multifocal cancers, as seen in Stage A (incidental) carcinoma, had a significantly weaker association with severe dysplasia as compared with central, intermediate‐grade, multifocal tumors or peripheral multifocal tumors of any grade.
AB - Severe dysplasia was studied in totally embedded radical prostatectomy specimens from 40 Stage B, intermediate‐grade prostate cancers. All 40 cases had severe dysplasia which varied in amount (extensive in 35% of cases; intermediate in 55%; minimal in 10%). Severe dysplasia was predominantly concentrated in peripheral and posterior regions of the gland. Those cases with extensive severe dysplasia had more multifocal small cancers (14.6/case) compared with cases with intermediate (7.5/case) or minimal severe dysplasia (5.5/case). Most dominant tumor nodules had some intermingled severe dysplasia, and in 30% of the dominant tumor nodules, intermingled severe dysplasia occupied between 10% and 25% of the tumor nodule. Severe dysplasia was located next to the dominant tumor nodule in all cases. Nineteen percent of dominant tumor nodules had extensive adjacent severe dysplasia ranging from 5 to 14 mm in maximum diameter, showing that the potential exists for needle biopsy of prostate cancers to obtain only severe dysplasia. These data show a close relationship between severe dysplasia and Stage B cancers. In contrast, centrally located low‐grade multifocal cancers, as seen in Stage A (incidental) carcinoma, had a significantly weaker association with severe dysplasia as compared with central, intermediate‐grade, multifocal tumors or peripheral multifocal tumors of any grade.
UR - http://www.scopus.com/inward/record.url?scp=0025322678&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025322678&partnerID=8YFLogxK
U2 - 10.1002/1097-0142(19900515)65:10<2328::AID-CNCR2820651027>3.0.CO;2-O
DO - 10.1002/1097-0142(19900515)65:10<2328::AID-CNCR2820651027>3.0.CO;2-O
M3 - Article
C2 - 2346917
AN - SCOPUS:0025322678
SN - 0008-543X
VL - 65
SP - 2328
EP - 2337
JO - Cancer
JF - Cancer
IS - 10
ER -