首页> 美国卫生研究院文献>Journal of Anatomy and Physiology >Epididymal-testicular fusion anomalies in cryptorchidism are associated with proximal location of the undescended testis and with a widely patent processus vaginalis
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Epididymal-testicular fusion anomalies in cryptorchidism are associated with proximal location of the undescended testis and with a widely patent processus vaginalis

机译:隐睾症的附睾-睾丸融合异常与睾丸未降位的近端位置以及广泛的阴道未发育过程有关

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摘要

Past studies documented the presence of epididymal/testicular fusion anomalies and persistence of a patent processus vaginalis in a small case-series of cryptorchid and/or hydrocele patients. The primary aim of this study was to determine the prevalence of the epididymal/testicular anomalies in a series of more than 1000 cryptorchid patients compared with controls. Secondary aims were: (i) to investigate the association between the cryptorchidism and the patency of p. vaginalis; and (ii) to correlate the epididymal/testicular fusion anomalies with the position of the testis and with the patency of the p. vaginalis. The clinical and surgical data of 1002 cryptorchid patients and 230 controls were retrospectively retrieved and analysed. Epididymal/testicular fusion anomalies were classified as: (i) normal anatomy; (ii) minor anomalies; and (iii) major anomalies. Statistical analysis was performed using the Student's t-test and Chi-square tests. The prevalence of the epididymal/testicular fusion anomalies was higher in the cryptorchid group compared with that of the control group (minor and major anomalies in cryptorchids vs. controls, respectively: 42.2 vs. 5.6% and 9.3 vs. 1.6%, P < 0.0001). Moreover, we documented a correlation of these anomalies with a more proximal localization of the testis (minor and major anomalies in proximal vs. distal location of the testis, respectively: 62.5 vs. 34.8% and 19.1 vs. 6.3%, P < 0.0001) and with the persistence of a widely patent p. vaginalis (minor and major anomalies in widely patent p. vaginalis vs. narrow duct, respectively: 51.7 vs. 42.2 and 11.9% vs. 7.8%, P < 0.001). In conclusion, the epididymal/testicular fusion anomalies were strongly associated with cryptorchidism and the persistence of a widely patent peritoneal vaginal duct. Although it remains unclear whether these anomalies cause non-descent of the testis or, conversely, result from the cryptorchidism or from the persistence of a widely patent duct, our data re-enforce this association.
机译:以往的研究表明,在一小系列隐睾和/或鞘膜积液患者中,附睾/睾丸融合异常的存在和阴道未闭过程的持续存在。这项研究的主要目的是确定与对照组相比,一系列1000多名隐睾患者的附睾/睾丸异常的患病率。次要目标是:(i)研究隐睾症与p的开放性之间的关联。阴道(ii)将附睾/睾丸融合异常与睾丸的位置以及p的通畅性联系起来。阴道。回顾性分析了1002例隐睾患者和230例对照的临床和手术资料。附睾/睾丸融合异常分类为:(i)正常解剖; (ii)轻微异常; (iii)重大异常。使用学生t检验和卡方检验进行统计分析。隐睾组的附睾/睾丸融合异常患病率高于对照组(隐睾与对照组的轻微异常和主要异常分别为42.2 vs.5.6%和9.3 vs.1.6%,P <0.0001 )。此外,我们记录了这些异常与睾丸近端定位的相关性(睾丸近端与远端位置的较小和主要异常分别为:62.5 vs. 34.8%和19.1 vs. 6.3%,P <0.0001)并拥有广泛的专利p。阴道炎(广泛专利的阴道阴道炎与狭窄导管的微小异常和主要异常分别为:51.7对42.2和11.9%对7.8%,P <0.001)。总之,附睾/睾丸融合异常与隐睾症以及广泛的腹膜阴道阴道导管的持续存在密切相关。尽管目前尚不清楚这些异常是否导致睾丸未下降,或者相反是由隐睾症或广泛存在的专利导管引起的,但我们的数据仍加强了这种联系。

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