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遗传性前列腺癌的病理特征

Pathological features of hereditary prostate cancer.

作者信息

Bastacky S I, Wojno K J, Walsh P C, Carmichael M J, Epstein J I

机构信息

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-2101.

出版信息

J Urol. 1995 Mar;153(3 Pt 2):987-92.

PMID:7853589
Abstract

The aim of this study was to characterize the pathological features of hereditary prostate cancer, a recently recognized variant of prostate cancer with an autosomal dominant inheritance of a rare highly penetrant gene associated with early onset of disease. We compared the histology at radical prostatectomy of clinical stage T2 prostate cancer, including its relationship to prostatic intraepithelial neoplasia, in men with a family history of prostate cancer to those without a family history of prostate cancer. Three cohorts (hereditary, familial and sporadic) were identified based on pedigree analysis. A hereditary subgroup (28 patients) met 1 of the following 3 criteria: 1) cluster of greater than 3 affected relatives within the nuclear family, 2) occurrence of prostate cancer in each of 3 generations in either the proband paternal or maternal lineage, or 3) a cluster of 2 relatives affected at an early age of less than 55 years. This subgroup was compared to an age-matched subgroup with family history of prostate cancer (26 patients) yet the aforementioned conditions for inclusion within the hereditary subgroup were not met and to a sporadic subgroup without a family history of prostate cancer (27 patients). All parameters were statistically similar among the groups except that hereditary and familial group multifocal tumors were of lower grade (p = 0.0001), sporadic cases had a greater proportion of small multifocal cancers associated with prostatic intraepithelial neoplasia (p = 0.02) and the familial group had a weaker correlation between total tumor volume and grade. In conclusion, our analysis failed to demonstrate substantial pathological differences among hereditary, familial and sporadic forms of prostate cancer. Rather, our data are remarkable for the wide range of all parameters studied in each group. Even the sporadic cases had features, such as increased numbers of precursor lesions and tumor multifocality, which in other organs are commonly associated with either hereditary cancer or cancer arising in a field effect due to diffuse exposure to a carcinogen.

摘要

本研究的目的是描述遗传性前列腺癌的病理特征,这是一种最近才被认识到的前列腺癌变体,具有常染色体显性遗传,由一个与疾病早发相关的罕见高外显率基因引起。我们比较了有前列腺癌家族史的男性与无前列腺癌家族史的男性在根治性前列腺切除术中临床分期为T2期前列腺癌的组织学情况,包括其与前列腺上皮内瘤变的关系。通过系谱分析确定了三个队列(遗传性、家族性和散发性)。一个遗传性亚组(28例患者)符合以下三项标准中的一项:1)核心家庭中有超过3名受影响亲属的聚集;2)先证者父系或母系三代中每一代都发生前列腺癌;或3)有2名亲属在55岁以下的早年受影响的聚集。将该亚组与年龄匹配的有前列腺癌家族史但不符合遗传性亚组上述纳入条件的亚组(26例患者)以及无前列腺癌家族史的散发性亚组(27例患者)进行比较。除遗传性和家族性组多灶性肿瘤分级较低(p = 0.0001)、散发性病例中与前列腺上皮内瘤变相关的小多灶性癌比例较高(p = 0.02)以及家族性组总肿瘤体积与分级之间的相关性较弱外,各组之间的所有参数在统计学上均相似。总之,我们的分析未能证明遗传性、家族性和散发性前列腺癌在病理上存在实质性差异。相反,我们的数据在每组研究的所有参数范围之广方面引人注目。即使是散发性病例也有一些特征,如前体病变数量增加和肿瘤多灶性,在其他器官中,这些特征通常与遗传性癌症或由于广泛接触致癌物而在场效应中发生的癌症有关。

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