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Ultrasonography in Diagnosis of Congenital Absence of the Vas Deferens

机译:超声检查诊断先天性输精管狭窄

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BACKGROUND Congenital absence of the vas deferens is an important cause of obstructive azoospermia, and the lack of an imaging diagnostic test is a critical problem. The aim of this study is to discuss the use of ultrasonography in congenital absence of vas deferens, including dysplasia of the epididymis and the seminal vesical. MATERIAL AND METHODS Five fresh spermatic cord specimens were detected by ultrasonography (US) to evaluate the image of the spermatic cord segment of the vas deferens. Fifty normal males had scrotal US to confirm whether the normal spermatic cord segment of the vas deferens can be detected and to measure the internal and external diameter on the long axis view. Forty-six males clinically diagnosed as having congenital absence of vas deferens underwent scrotal US to evaluate the spermatic cord segment of the vas deferens and the epididymis. The seminal vesicals were detected with transrectal ultrasonography. We evaluated images of the vas deferens, epididymis, and seminal vesical. RESULTS Scrotal ultrasonography can distinguish the vas deferens from the other cord-like structures in the spermatic cord, and the vas deferens has a characteristic image. Scrotal ultrasonography detected all 50 normal males and measured the diameter. No statistically significant difference was found between the left and right measurements. In the 46 patients, the following anomalies were observed: 1) 42 cases of congenital bilateral absence of vas deferens; 2) 2 cases of congenital unilateral absence of the vas deferens; and 3) 1 case of congenital segmental absence of the vas deferens. All 46 cases were accompanied with epididymis and seminal vesical anomalies. CONCLUSIONS The spermatic cord segment of the vas deferens can be detected by US, which is a valuable tool in diagnosis of congenital absence of the vas deferens. Seminal vesical and epididymis anomalies often associated with congenital absence of the vas deferens were revealed by ultrasonography.
机译:背景技术先天性输精管缺失是阻塞性无精子症的重要原因,而缺乏影像学诊断测试是一个关键问题。这项研究的目的是讨论超声检查在先天性输精管缺失(包括附睾和精囊发育异常)中的应用。材料与方法通过超声检查(US)检测了五个新鲜的精索标本,以评估输精管精索段的图像。五十名正常男性进行阴囊超声检查,以确认是否可以检测到输精管的正常精索段,并在长轴视图上测量内径和外径。经临床诊断为先天性输精管缺失的四十六名男性行阴囊超声检查以评估输精管和附睾的精索段。经直肠超声检查发现精囊。我们评估了输精管,附睾和精囊的图像。结果阴囊超声检查可以将输精管与精索中的其他索状结构区分开,并且输精管具有特征性图像。阴囊超声检查可检测全部50名正常男性,并测量其直径。在左右测量之间没有发现统计学上的显着差异。在这46例患者中,观察到以下异常:1)42例先天性双侧输精管缺失。 2)2例先天性单侧输精管缺失; 3)1例先天性节段性输精管缺失。全部46例均伴有附睾和精囊异常。结论输精管的精索段可通过US检测,这是诊断先天性输精管缺失的有价值的工具。超声检查可发现通常与先天性输精管缺失有关的精囊和附睾异常。

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