Cribiform and intraductal carcinoma in hereditary prostate cancer: clinical and pathological analysis of 20 cases.

IF 1.5 Q3 UROLOGY & NEPHROLOGY American journal of clinical and experimental urology Pub Date : 2024-04-15 eCollection Date: 2024-01-01 DOI:10.62347/XOIN3964
Yuhao Zhang, Yutao Zhang, Minjing Shi, Xiaoyan Liu, Han Zhang, Ping Zhao, Guoping Ren
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Abstract

Cribiform and intraductal carcinoma are patterns of aggressive prostate carcinoma. This study investigated the clinical and pathological features of hereditary prostate cancer. Twenty cases of hereditary prostate cancer from 11 family lines treated at the First Affiliated Hospital of Zhejiang University School of Medicine between 2016-2022 were included to summarize the clinical and pathological features by analyzing clinical information including follow up the survival of the patients and pathological features. Of the 20 hereditary prostate cancer cases, 19 were radical prostate specimens and 1 was a biopsy specimen. The mean age at diagnosis of the patients was 67.55 years and the mean PSA was 15.44 ng/ml, of which 10 cases had PSA ≥ 10 ng/ml and 5 cases had PSA ≥ 20 ng/ml. Of the 19 radical prostate specimens, Gleason cribriform pattern (Gleason grade 4) of PCa is observed in 15 cases (78.95%), and intraductal carcinoma, usually a rare form, is seen in 9 cases (47.3%). Two cases demonstrated pelvic lymph node metastasis, and 7 cases (35%) belonged to high-risk or very high-risk PCa. One case (5.26%) showed partial deletion of expression of RB1, and 13 cases (68.42%) showed deletion of expression of PTEN. Follow-up was 4-90 months, 2 cases had biochemical recurrence and 1 case died from prostate cancer. The mean age at diagnosis of this group of patients with hereditary prostate cancer was 67.55 years, the mean preoperative PSA was 15.44 ng/ml, and their histomorphology was characterized by a high percentage of intraductal carcinoma and cribriform pattern of the prostate.

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遗传性前列腺癌中的楔形癌和导管内癌:20 例病例的临床和病理分析。
楔形癌和导管内癌是侵袭性前列腺癌的模式。本研究调查了遗传性前列腺癌的临床和病理特征。纳入浙江大学医学院附属第一医院2016-2022年间收治的11个家系的20例遗传性前列腺癌患者,通过分析患者的随访生存期等临床资料和病理特征,总结遗传性前列腺癌的临床和病理特征。在20例遗传性前列腺癌病例中,19例为前列腺癌根治术标本,1例为活检标本。患者确诊时的平均年龄为67.55岁,平均PSA为15.44纳克/毫升,其中10例PSA≥10纳克/毫升,5例PSA≥20纳克/毫升。在 19 例前列腺癌根治术标本中,15 例(78.95%)观察到 PCa 的格里森楔形模式(格里森 4 级),9 例(47.3%)观察到导管内癌,导管内癌通常是一种罕见的形式。2 例病例出现盆腔淋巴结转移,7 例(35%)属于高危或极高危 PCA。1例(5.26%)表现为RB1部分缺失,13例(68.42%)表现为PTEN缺失。随访时间为 4-90 个月,2 例生化复发,1 例死于前列腺癌。这组遗传性前列腺癌患者确诊时的平均年龄为 67.55 岁,术前 PSA 平均值为 15.44 ng/ml,组织形态学特征为导管内癌和前列腺楔形形态比例较高。
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