Bostwick David G, Liu Lina, Brawer Michael K, Qian Junqi
Rev Urol. 2004 Fall;6(4):171-9.
High-grade prostatic intraepithelial neoplasia is considered the most likely precursor of prostatic carcinoma. The only method of detection is biopsy; prostatic intraepithelial neoplasia (PIN) does not significantly elevate serum prostate-specific antigen concentration and cannot be detected by ultra-sonography. The incidence of PIN in prostate biopsies averages 9% (range, 4%-16%), representing 115,000 new cases of PIN diagnosed each year in United States. PIN has a high predictive value as a marker for adenocarcinoma, and its identification warrants repeated biopsy for concurrent or subsequent invasive carcinoma. Carcinoma will develop in most patients with PIN within 10 years. PIN is associated with progressive abnormalities of phenotype and genotype that are intermediate between normal prostatic epithelium and cancer, indicating impairment of cell differentiation and regulatory control with advancing stages of prostatic carcinogenesis. Androgen deprivation therapy decreases the prevalence and extent of PIN, suggesting that this form of treatment may play a role in chemoprevention.
高级别前列腺上皮内瘤变被认为是前列腺癌最可能的前驱病变。唯一的检测方法是活检;前列腺上皮内瘤变(PIN)不会显著提高血清前列腺特异性抗原浓度,也无法通过超声检查检测到。前列腺活检中PIN的发生率平均为9%(范围为4%-16%),在美国每年有115,000例新诊断的PIN病例。PIN作为腺癌的标志物具有较高的预测价值,识别出PIN需要对同时存在或随后发生的浸润性癌进行重复活检。大多数PIN患者在10年内会发展为癌症。PIN与表型和基因型的进行性异常有关,这些异常介于正常前列腺上皮和癌症之间,表明随着前列腺癌发生阶段的推进,细胞分化和调控受到损害。雄激素剥夺疗法可降低PIN的发生率和范围,表明这种治疗形式可能在化学预防中发挥作用。