对患有睾丸微石症和其他癌症风险因素的男性进行睾丸活检:病例系列。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-02-20 DOI:10.1111/andr.13610
Rasmus Hassing Frandsen, Emil Durukan, Elena von Rohden, Christian Fuglesang S Jensen, Andreas Key Milan Thamsborg, Nessn Azawi, Mikkel Fode
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引用次数: 0

摘要

背景:睾丸微石症是指睾丸实质中出现小钙化。睾丸微石症与睾丸癌的前兆--原位生殖细胞瘤之间的关系尚不清楚:目的:确定男性睾丸微石症患者生殖细胞原位肿瘤的发病率,并根据男性不育/精液质量下降、睾丸萎缩和隐睾病史等风险因素评估睾丸活检的适应症:该回顾性病例系列包括2007年至2021年间在丹麦三家医院接受睾丸活检的所有确诊为睾丸微石症的患者。研究人员查阅了167名患者的病历,收集了患者人口统计学、睾丸微石症特征、风险因素、组织学检查结果和治疗方法等方面的数据。主要结果指标是与各风险因素相关的生殖细胞原位肿瘤发病率。数据采用描述性统计进行分析。采用逻辑回归法检测睾丸微石症和睾丸萎缩患者发生生殖细胞原位瘤变的几率:结果:167 例患者中有 13 例(7.8% [95% 置信区间:4.3, 13.2])发现生殖细胞原位瘤。其中有 11 人患有睾丸萎缩,导致该组患者的发病率明显高于其他风险因素(几率比 9.36 [95% 置信区间:2.41, 61.88];P = 0.004):该研究是迄今为止对因睾丸微石症和其他风险因素而接受睾丸活检的男性进行的最大规模研究。结论:这项研究发现,患有睾丸微小结石和其他风险因素的男性睾丸活检患者中,睾丸原位生殖细胞瘤患者的绝对数量相对较少:本研究发现,患有睾丸微石症和睾丸萎缩的男性罹患生殖细胞原位肿瘤的风险较高。此外,我们的研究结果表明,对于同时患有不育症和双侧睾丸微石症的男性,应考虑进行活检。我们的研究结果不支持对患有睾丸微石症和其他风险因素的男性进行睾丸活检。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Testicular biopsies in men with testicular microlithiasis and additional risk factors for cancer: A case series.

Background: Testicular microlithiasis is the presence of small calcifications in the testicular parenchyma. The association between testicular microlithiasis and germ cell neoplasia in situ, a precursor to testicular cancer, is still unclear.

Objectives: To determine the incidence of germ cell neoplasia in situ in men with testicular microlithiasis and evaluate the indication for testicular biopsy according to risk factors in the form of male infertility/reduced semen quality, testicular atrophy, and history of cryptorchidism.

Materials and methods: This retrospective case series included all patients diagnosed with testicular microlithiasis who underwent testicular biopsies at three hospitals in Denmark between 2007 and 2021. The medical records of 167 patients were reviewed, and data on patient demographics, testicular microlithiasis characteristics, risk factors, histological findings, and treatments were collected. The main outcome measure was the incidence of germ cell neoplasia in situ in relation to each risk factor. The data were analyzed using descriptive statistics. Logistic regression was used to examine the odds ratio of germ cell neoplasia in situ in patients with testicular microlithiasis and testicular atrophy.

Results: Germ cell neoplasia in situ was found in 13 out of 167 patients (7.8% [95% confidence interval: 4.3, 13.2]). Eleven of these had testicular atrophy resulting in a significantly higher incidence in this group than other risk factors (odds ratio 9.36 [95% confidence interval: 2.41, 61.88]; p = 0.004).

Discussion: The study comprises the largest cohort to date of men who have undergone testicular biopsies because of testicular microlithiasis and additional risk factors. Limitations include its retrospective design, and relatively low absolute numbers of patients with germ cell neoplasia in situ on biopsies.

Conclusion: This study found that men with testicular microlithiasis and testicular atrophy are at an increased risk of germ cell neoplasia in situ. Additionally, our results indicate that biopsies should be considered in men with a combination of subfertility and bilateral testicular microlithiasis. Our findings do not support testicular biopsies for men with testicular microlithiasis and other risk factors.

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CiteScore
7.20
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