Cohen R J, McNeal J E, Baillie T
Urological Research Centre, University of Western Australia, Perth, Western Australia, Australia.
Prostate. 2000 Apr 1;43(1):11-9. doi: 10.1002/(sici)1097-0045(20000401)43:1<11::aid-pros3>3.0.co;2-b.
Cribriform prostatic intraepithelial neoplasia (C-PIN) identifies a unique histological pattern: dysplastic cells line ductal/acinar walls but also span across gland lumens. C-PIN is distinct from other forms of dysplasia; it is seldom seen except within invasive cancer, it is more frequent in larger/higher-grade cancers; and it appears to contribute independently to aggressive behavior. Hence, C-PIN may represent a separate, more aggressive entity: intraductal carcinoma of the prostate (IDC-P). Here, support for that distinction stems from a histologic/biologic subclassification of IDC-P, whose elements are linked to features of invasive cancer.
Histologic criteria were tested against 26 radical prostatectomies, using immunostains for prostate-specific antigen, MUC-2, androgen receptor (differentiation), and Ki-67 (proliferation). Invasive cancer grade, stage, and follow-up were compared.
Architecture of the central (luminal) cell compartment defined three subclasses of IDC-P: A (trabecular), B (cribriform), and C (solid/comedo), which represented progressive dedifferentiation with a reciprocal increase in proliferation. The IDC-P subpattern correlated with cancer stage, grade, and clinical course.
IDC-P is a separate entity, distinct from PIN; cancers associated with IDC-P are more aggressive than those associated with only PIN. It comprises a spectrum of histological patterns which appear to be determined in concert with invasive cancer, whose prognosis it worsens.
筛状前列腺上皮内瘤变(C-PIN)具有独特的组织学模式:发育异常的细胞排列于导管/腺泡壁,但也跨越腺腔。C-PIN不同于其他发育异常形式;除浸润性癌内少见外,在较大/高级别癌中更常见;且似乎独立地促成侵袭性行为。因此,C-PIN可能代表一种单独的、更具侵袭性的实体:前列腺导管内癌(IDC-P)。在此,对这种区分的支持源于IDC-P的组织学/生物学亚分类,其要素与浸润性癌的特征相关。
对26例根治性前列腺切除术的标本进行组织学标准检测,使用前列腺特异性抗原、MUC-2、雄激素受体(分化)和Ki-67(增殖)的免疫染色。比较浸润性癌的分级、分期和随访情况。
中央(管腔)细胞区室的结构定义了IDC-P的三个亚类:A(小梁状)、B(筛状)和C(实性/粉刺样),它们代表了逐渐的去分化,增殖相应增加。IDC-P的亚模式与癌症分期、分级和临床病程相关。
IDC-P是一种与PIN不同的单独实体;与IDC-P相关的癌症比仅与PIN相关的癌症更具侵袭性。它包括一系列组织学模式,这些模式似乎与浸润性癌共同决定,其预后更差。