性腺功能低下男性隐匿性前列腺癌的病理特征

Ping L. Zhang, G. Bubley, M. Upton, A. Morgentaler, W. DeWolf, S. Rosen
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引用次数: 3

摘要

目的:对于游离睾酮水平低(< 1.5 ng/dl)的性腺功能低下男性,雄激素治疗具有潜在危险,因为外源性雄激素可能刺激隐匿性前列腺腺癌(PA)。我们之前的研究报告了在前列腺特异性抗原(PSA)水平正常且直肠指检(DRE)结果正常的性腺功能低下男性中隐匿性PA(14%)的发生率。本研究的目的是检查性腺功能低下患者前列腺切除术标本中PA的程度和性质。材料与方法:将这14例患者(性腺功能低下组)的PA与对照组(n = 14)进行比较。两组患者的平均年龄、Gleason评分和PA的核心受累百分比相似。随后,对两组前列腺切除术标本中的PA进行分析,并对雄激素受体、PSA和前列腺酸性磷酸酶的免疫组化切片进行比较。结果:正如预期的那样,性腺功能低下组患者的PSA和游离睾酮水平明显低于对照组(PSA分别为2.32±0.60 ng/ml和8.06±1.17 ng/ml;游离睾酮分别为1.17±0.09 ng/dl和1.74±0.20 ng/dl)。性腺功能低下患者的前列腺切除术标本(n = 9)显示,与对照前列腺切除术标本(n = 14)(21%的边缘阳性,42%的神经周围浸润,21%的单侧肿瘤,58%的双侧肿瘤)相比,PA的范围较小(0%阳性边缘,11%神经周围浸润,78%单侧肿瘤,22%双侧肿瘤)。然而,使用抗雄激素受体、抗psa和抗前列腺酸性磷酸酶抗体的免疫组化研究显示,两组的癌细胞染色强度相当。结论:在DREs和PSA水平正常的性腺功能减退患者中,PA似乎不那么广泛,但在形态学上与正常患者没有不同,应以同样的方式治疗。在这些性腺功能低下的患者中,隐匿性前列腺炎的发生率很高,因此在雄激素替代治疗前进行前列腺活检筛查非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathologic Features of Occult Prostatic Carcinoma in Hypogonadal Men
Objectives: Androgen therapy in hypogonadal men with low free testosterone levels (< 1.5 ng/dl) is potentially dangerous because exogenous androgen may stimulate occult prostatic adenocarcinoma (PA). Our previous study reported occult PA (14% incidence) in hypogonadal men with normal prostate specific antigen (PSA) levels and normal findings on digital rectal examination (DRE). The purpose of the current study was to examine the extent and nature of PA in prostatectomy specimens of hypogonadal patients. Materials and Methods: PA in these14 patients (the hypogonadal group) was compared to a control group of patients (n = 14). The two groups of patients were matched with similar mean ages, Gleason scores, and percentage of core involvement by PA. Subsequently, PA in prostatectomy specimens was analyzed in the two groups with additional comparison of immunohistochemical sections for androgen receptors, PSA, and prostatic acid phosphatase. Results: As expected, patients in the hypogonadal group had significantly lower levels of PSA and free testosterone than those in the control group (PSA 2.32 ± 0.60 ng/ml versus 8.06 ± 1.17 ng/ml, respectively; free testosterone 1.17 ± 0.09 ng/dl versus 1.74 ± 0.20 ng/dl, respectively). Prostatectomy specimens in hypogonadal patients (n = 9) showed a less extensive PA (0% positive margins, 11% perineural invasion, 78% unilateral tumor, and 22% bilateral tumor) compared to control prostatectomy specimens (n = 14) (21% positive margins, 42% perineural invasion, 21% unilateral tumor, and 58% bilateral tumor). However, immunohistochemical studies using anti-androgen receptor, anti-PSA and anti-prostatic acid phosphatase antibodies showed that carcinoma cells stained with equivalent intensity in both groups. Conclusions: PA in hypogonadal patients who had normal DREs and PSA levels appears to be less extensive but otherwise is not morphologically different than usual and should be treated in the same manner. The high incidence of occult PA in these hypogonadal patients makes screening prostate biopsies important before the androgen replacement therapy.
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