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[前列腺“发育异常”改变的诊断价值]

[The diagnostic value of "dysplastic" changes in the prostate].

作者信息

Mehlhorn J

机构信息

Institut für Pathologie Stollberg/Sachsen.

出版信息

Zentralbl Pathol. 1991;137(5):395-401.

PMID:1801908
Abstract

The technique of serial section was used in systematic investigations of prostates obtained from 450 individuals who had died at the age of 40 to over 80 years. This was done, with a view to clearing up the precancerous potential of so-called dysplastic lesions (intraductal dysplasia, prostatic intraepithelial neoplasia). All accompanying pathomorphological findings were recorded, at the same time, with the totality of data being jointly evaluated and statistically processed by computerised methods. So-called dysplastic alterations were recordable from 57% of all cases (26% to 80%), with incidence rates growing along with advancing age and statistical security depending on age at large. Slight dysplasia was recorded from 41% of all cases, with an average of 2.6 foci (10 foci maximum) to one prostate. Severe dysplasia was recorded from 42% of all cases, with an average of 3.8 foci (24 maximum) to one prostate. The area of 90% of all foci was up to 4 mm2 (16 mm2 maximum in cases of slight dysplasia and 60 mm2 in severe cases). Dysplasia was localised in the posterior region of the organ in 60% of all cases and was detected in the central region in 8% maximum. Carcinoma was identified in 133 cases, with 114 of them (86%) being associated with dysplasia. Dysplasia was also detected in 45% of cases without carcinoma. Severe dysplasia was present in 79% of all carcinoma cases and in 26% of no-carcinoma cases. Slight dysplasia, on the other hand, was recordable form 7% of carcinoma cases and 19% of no-carcinoma cases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

连续切片技术被用于对450例年龄在40岁至80多岁死亡个体的前列腺进行系统研究。这样做是为了弄清楚所谓发育异常病变(导管内发育异常、前列腺上皮内瘤变)的癌前潜能。同时记录所有伴随的病理形态学发现,并通过计算机方法对所有数据进行联合评估和统计处理。在所有病例的57%(26%至80%)中可记录到所谓的发育异常改变,发病率随年龄增长而上升,且总体统计安全性取决于年龄。在所有病例的41%中记录到轻度发育异常,每个前列腺平均有2.6个病灶(最多10个病灶)。在所有病例的42%中记录到重度发育异常,每个前列腺平均有3.8个病灶(最多24个)。所有病灶的90%面积达4平方毫米(轻度发育异常病例中最大为16平方毫米,重度病例中为60平方毫米)。在所有病例的60%中,发育异常位于器官的后部区域,在中央区域最多检测到8%。在133例中发现了癌,其中114例(86%)与发育异常相关。在无癌病例的45%中也检测到发育异常。在所有癌病例的79%和无癌病例的26%中存在重度发育异常。另一方面,在7%的癌病例和19%的无癌病例中可记录到轻度发育异常。(摘要截断于250字)

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